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Microscopy ListServer ArchivesFile Requested = 9502.txt
Retrival Software
Version=NJZ07060908
From: Riitta Harjula: rharjula-at-cc.oulu.fi Date: Wed, 1 Feb
199514:38:54 +0200 (EET)
Contents Retrieved from Microscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Subscribe Riitta Harjula
Riitta.Harjula-at-oulu.fi
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From: Marc Brande: brande-at-sdsc.edu Date: Wed, 1 Feb 199511:39:27
-0800 (PST)
Subject: Confocal Scope in San Diego Contents Retrieved
fromMicroscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Microscopy List {microscopy-at-aaem.amc.anl.gov} ,
Confocal Microscopy List {confocal-at-ubvm.bitnet}
Message-Id:{Pine.3.05.1.9502011127.A7624-9100000-at-pauline.sdsc.edu}
Mime-Version:1.0
Content-Type: TEXT/PLAIN; charset=US-ASCII
I am in need of access toa confocal scope in the San Diego area.
Would
anyone know of a lab that has oneand who to contact? Thanks in
advance
for your help.
Marc
Marc C.Brande, M.S. SD3D Email List:3D Imaging
San Diego 3D Imaging Group
Tosubscribe/unsubscribe:listserv-at-bobcat.etsu.edu
3840 Camino Lindo Topost a message:sd3d-at-bobcat.etsu.edu
San Diego, CA 92122 Email:BRANDE-at-SDSC.EDU
Voice:619-587-4830
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From: tivol-at-tethys.ph.albany.edu Date: Wed, 01 Feb 1995 16:45:52
EST
Subject: RE: EMLab scheduling ContentsRetrieved from Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Jan Coetzee asks about electronic vs. "dog-eared diary" for
schedules.
Dear Jan,
We use a large desk calendar ourselves. It seemseasier, since
there
are frequent changes, and everyone can check it instantly.I'm sure
that a
calendar page on a computer might do as well, but when a usercalls,
we are
not always booted up, so it would take us more time than it
doeswith paper
and pencil. If your scopes are computer-controlled, it might
savesome time
and/or effort to have schedules on the same computer--e.g.
thecomputer could
dial a user you need to contact re schedule changes--but we havenot
thought
this to be worthwhile for us. Sometimes low-tech works
verywell!
Yours,
Bill Tivol
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From: tivol-at-tethys.ph.albany.edu Date: Wed, 01 Feb 1995 17:43:19
EST
Subject:Peltier devices ContentsRetrieved from Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Jan Coetzee inquired about mfgrs of pltrs.
Dear Jan,
Melcor makes them. Their address, phone & fax are
1040Spruce Street
Trenton NJ 08648-4587
UnitedStates of America (our USA)
(609) 393-4178 (phone)
(609) 393-9461 (fax)
One potential problem is that Peltiers have alimited delta-T, and
can
get very expensive. I asked Melcor about setting up acold stage for
epitax-
ial deposition in a vacuum, and there was nothing whichwould get
cold enough.
Furthermore, if you wish to thermostat the device, youneed to use a
cooler
which has a 100% duty cycle and output currentproportional to the
difference
between target and actual temperatures. Wefound this out when we
installed
Peltiers in our darkroom as heaters/coolers tomaintain developer
temperature.
The intermittant current put out by the usualcommercially available
devices
blew the Peltiers out! Otherwise, Peltiers aremarvelous devices.
Good luck.
Yours,
Bill Tivol
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From: WayneWNB-at-aol.com Date: Wed, 1 Feb 1995 22:28:40
-0500
Subject: Electron MicroscopePictures ContentsRetrieved from
Microscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {25020121201502-at-vms2.macc.wisc.edu}
G'day Subscribers...
I've received this request for help onlocating micrographs
of bacteria. I could not help this individual. So isthere
anyone out there that can?
Cheers....Nestor Z.
Your FriendlyNeighborhood SysOp
=====================================
P.S.
I'm working on concept of adding an Image Library to
theSoftware
Library. When it's ready for contributions I'll post
a message totheListserver....
====================================
Ineed an electron microscope picture of Methanosarcina
barkeriand
Methanobacterium wolfei. I called the University of California
atBerkeley
and they gave me your address. They said that they don't keep a
fileof
their past work and would charge $300 per picture to do the work
again.I'm
fairly certain that the pictures already exist somewhere. I
believe
that
NASA may have some of them but I don't know who to ask there .
Thank youfor
any help in getting any pictures of the twobacteria.
------------------
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From: Richard Lee: richard_lee-at-qmgate.anl.gov Date: 2 Feb1995
13:01:13 -0600
Subject: subscibe Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {n1420392126.63194-at-qmgate.anl.gov}
subscibe2/2/95
subscribe, PLEASE!
12:46 PM
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9/125
From: richard.easingwood-at-stonebow.otago.ac.nz (Richard
Easingwood) Date: Fri, 3 Feb 1995 08:56:44+1100
Subject: TEM:Staining glycogen in sections Contents Retrieved from
Microscopy ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {199502022051.JAA12437-at-arwen.otago.ac.nz}
X-Sender: st004718-at-brandywine.otago.ac.nz
Mime-Version: 1.0
Content-Type: text/plain; charset="us-ascii"
One of EM Unit users is studyingdeveloping Red deer. The samples we
are
examining are skull and pedicle(developing antler) taken from the
deer at
set time intervals over atwo yearperiod. The samples are
processed
routinely, ie glutaraldehydefixed,decalcified, OsO4 post fixed,
uranyl
acetate bloc stain, dehydrated andembedded in Agar 100 epoxy
resin.
Our problem is that it now seems to bethat the glycogen content is
of some
significance to the investigation.Unfortunately the above process
is not
ideal for showing the glycogen.
Somerecently processed samples using potassium ferrocyanide with
the
osmium arebrilliant however we would like to enhance the glycogen
in the
previousblocks.
Does anyone out there know a method to enhance "unstainable"
glycogen
in
ultrathin sections?
Thanks in anticipation.
AllanMitchell
South Campus EM Unit
allan.mitchell-at-stonebow.otago.ac.nz
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From: randy nessler: rnessler-at-emiris.iaf.uiowa.edu Date: Thu,2
Feb 1995 14:51:56 -0600 (CST)
Subject: Site for JCPDS Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Does anyone know of a site that I can download filesfrom the
JCPDS?
Randy Nessler
rnessler-at-emiris.iaf.uiowa.edu
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From: Doug Arrell: ARRELL-at-jrc.nl Date: Fri, 3 Feb 199508:31:16
GMT+0200
Subject: Re: Convert PS files Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
} I am looking for a way to convert my PostScriptfiles into
"regular" image
} files. Does someone know of such siftwares oneither Mac or Unix
platforms?
} Any information would be appreciated.
}
Do you mean postscript or encapsulated postscript? If postscript
then
oneof the postscript interpreters available should do it. I use
one
an a PCcalled GoScript that outputs to TIFF files as well as
printers. I am not sure,but you should take a look at the GNU
Ghostscript interpreter that runs onvirtually anything -
certainly
on unix systems. If you mean encapsulatedpostscript (EPS) then
just
import the files into a Mac word processor such asWordPerfect
on
Microsoft Word and then copy and paste to whereever you
wantto.
+------------------------------------+
| Dr Douglas Arrell|
| Mechanical Performance and Joining |
| Institute for Advanced Materials|
| 1755 ZG Petten |
| Netherlands
|
| {ARRELL-at-JRC.NL} |
| Tel. (+31) 2246 5287|
| Fax (+31) 2246 1917 |
+------------------------------------+
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From: MicroToday-at-aol.com Date: Fri, 3 Feb 1995 08:58:20
-0500
Subject: Bacteria Micrographs Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Group -
Responding to an inquiry from Nestor, Custom
Medical Stock Photo is a
company which purchases micrographs and then sellsthem to
publications, etc.
They have a considerable inventory - in microscopy,and a number
"with"
bacteria.
Many readers may be interested in contactingthem and explore the
sale of
their micrographs. I have, of course, nofinancial interest in the
company.
Custom Medical Storck Photo,Inc.
3819 North Southport Ave
Chicago, IL 60613
Tel.: 312-248-3200
Fax: 312-248-7427
Regards,
Don Grimes, Microscopy Today
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From: Kris_Kavanau-at-dmcmail.ucsf.edu Date: Fri, 03 Feb 1995
10:03:40 PST
Subject: UranylGlass/FM Stds. ContentsRetrieved from Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {1995Feb03.100340.2874650620-at-dmcmail.ucsf.edu}
To: Microscopy-at-aaem.amc.anl.gov (M)
Subject:Time: 9:45 AM
OFFICE MEMO Uranyl Glass/FM Stds.Date: 2/3/95
Dear Microscopists,
Does anyone have any uranyl glass, or knowwhere it might be
obtained? I
have been told that it is no longer manufacturedcommercially. It
might be
an excellent "generic" fluorescence microscopycontrol.
Are there any commercially available, pre-mounted
fluorescencestandards
besides "MultiSpeck" from Molecular Probes? They are
veryconvenient, but
they are not ideal for our applications as DAPI, fluorescein,and
Texas Red
specific controls. Unfortunately, Flow Cytometry Standards Co.no
longer
makes pre-mounted standards.
I have been managing the UCSF coreflow and image cytometry facility
("Lab
for Cell Analysis") for 2 years, but Ihad no real QC for our
2
occasionally used fluorescence microscopes. Now Ineed to establish
QC
protocols for 6 additional multi-user, computerized
fluorescence (one
scanning confocal) microscopes in the "National
MolecularCytogenetics
Resource." I was surprised that so few standards (and
journalreferences)
seem to be available.
Any suggestions or comments would begreatly appreciated. Thank you
very
much. KrisKavanau; kavanau-at-dmc.ucsf.edu
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From: John Kloetzel: kloetzel-at-umbc.edu (John Kloetzel) Date:Fri,
3 Feb 1995 14:14:17 -0500
Subject: EM network Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
subscribe microscopy kloetzel-at-umbc.edu
** JAK**
****************************************************************************
John A. Kloetzel, Ph.D. {kloetzel-at-umbc.edu}
Department of Biological Sciences
University of Maryland Baltimore County (UMBC)
Catonsville, MD 21228-5329 USA
Phone: (410) 455-2247 or-3913 (Lab)
FAX: (410) 455-3875
****************************************************************************
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From: Dr. William Dentler,University of Kansas, Dept. of Cell
Biology, Date: Fri, 3 Feb 1995 15:24:59-0600
Subject: fix pepper redux Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {m0raUmA-00011cC-at-pegasus.cc.ucf.edu}
Afew months ago a thread ran on fixation and embedding pepper
contaminant
artefact in biological ultrathin sections. A colleague of mine read
the Pepper
Summary I compiled and sent me the following fixation protocols
that he hasused
successfully without pepper. Notice the first one in which
glutaraldehyde,
phosphate buffer AND OSMIUM are all mixed TOGETHER!
If anyone outthere wants a copy of my Pepper Summary, contact me
off-line at my
e-mail and Iwill zip a copy out toyou.
------------------------------------------------------------------------
"1. For fixing cilia in mammalian trachea, I have used an
"instantfixation"
method using a combination of osmium, phosphate buffer,
andglutaraldehyde - in
the cold - for many years and have never seen the pepperdescribed
in the Pepper
Summary you sent to me. Right - all that stuff in the
same buffer dumped on the
tissue. Works great, but may extract a bit of actin.
"The method I used was one described in a paper by Omnoto
and Kung inthe J. Cell Biol 87:33-46. I think it uses 50 mM
NaPhosphate,
pH 7.2, 2% OsO4,2% glutaraldehyde. Add the Osmium just before you
add
the tissue and fix onice for 10 min. If you want, you can remove
the
black fix after 10 min and addanother slug of fix for another 10
min but
that is optional.
"Omoto andKung used it to fix Paramecium and their cilia. I have
used it to
fixmammalian trachea (with their cilia). The advantage is that it
seems
to"freeze" cilia in position, as opposed to glutaraldehyde, in
which cells
actualy swim for a dab before either being fixed or dying (we fix
cells,
we don't kill them, do we?). The osmium does not penetrate for more
than
afew cell layers but, with epithelial tissue or single cells, it
does
not makemuch difference.
"I have never tried that fix method on Chlamydomonas or
Tetrahymena. Over the
last year I have done a lot of embedding of Chlamy andhave never
seen pepper.
For those beasts, I find that cacodylate gives thebest preservation
of the
cytoplasm, although others find that phosphate bufferworks fine
too.
I do fix with glutaraldehyde in culture medium (pretty
muchphosphate buffer),
overnight in glut in cacodylate, rinse a few times incacodylate,
then
into 0.5-1% OsO4 in cacodylate for 30-60 min on ice, rinsewith a
few
changes of water and into uranyl acetate for a few hours prior
todehydrating in
acetone and embedding in epon.
"I've also tried anothermethod in which you fix with glut in
phosphate buffer,
rinse, then incubateovernight in uranyl acetate (in water) at 70
degrees
C. It works on Chlamy andavoids osmium. It is supposed to eliminate
the
need for poststaining ofsections, but I did not find this to be
the
case. I believe that I once readthat the reason for staining
sections is
to put a dab of stain on structures
at the last surface of the plastic
that the beam sees before blasting throughthe objective lens. I
don't
know, but, for Chlamy, I usually use the more oldfashioned method
that I
gave you above. Pepper does not seem to be one of
myproblems."
------------------------------------------------------------------------
Contributed to MICROSCOPY by:
--
Gib Ahlstrand, MMSNewsletter Editor
Electron Optical Facility, University of Minnesota, Dept.Plant
Pathology
495 Borlaug Hall, St. Paul, MN 55108 (612)625-8249
612-625-9728 FAX, giba-at-puccini.crl.umn.edu
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From: tivol-at-tethys.ph.albany.edu Date: Fri, 03 Feb 1995 18:23:23
EST
Subject: Re:TEM film ContentsRetrieved from Microscopy Listserver
Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Dear Lucille,
I just got a number from Kodak for
technical questions, but they could
probably direct you to a distributer. Itis (800) 242-2424 x19. We
usually
use a local vendor, National Graphics, but Ihave not noticed a
great range
of prices with other vendors. Good luck.
Yours,
Bill Tivol
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From: Dr. Edmund Glaser: eglaser-at-umabnet.ab.umd.edu Date: Fri,
3Feb 1995 22:12:08 -0500 (EST)
Subject: Re: TEM film Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
I am not aware that "cheap" is an a.k.a. for "reliable".Please be
kind
to the English language.
On Fri, 3 Feb 1995, Lucille A.Giannuzzi wrote:
} Can anyone recommend a reliable (a.k.a. cheap) U.S.vendor for TEM
film?
}
} Thanks in advance,
} Lucille Giannuzzi
}
}
}*************************************************************************
}Lucille A. Giannuzzi, Ph.D.
}
} Dept. of Mechanical and Aerospace Eng.phone (407) 823-5770
} University of Central Florida fax(407) 823-0208
} 4000 Central Florida Blvd. email lag-at-pegasus.cc.ucf.edu
} Orlando, FL 32816-2450 USA
}*************************************************************************
}
}
}
}
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From: Karpura V Kommineni: komminen-at-student.msu.edu Date: Sun, 5
Feb1995 12:32:08 -0500 (EST)
Subject: immunolabeling of wood Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {9502051732.AA72211-at-student1.cl.msu.edu}
DDoes anyone know about work done on immunolabelling of wood tissue
offruit
trees. I'm interested in any kind of information I can get
onfixation,
embedding and the labelling procedure. I plan to be using
ProteinA-colloidal
gold to tag the antibody.I'll be using a confocal microscope for
thisstudy.If
anyone knows any work done in this area could you please send
methe
references. Thank you in advance.
my email address: komminen-at-student.msu.edu
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From: Ian Hall: hall-at-me.udel.edu Date: Mon, 6 Feb 199508:31:26
-0500 (EST)
Subject: WDS Software Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Dear Fellow Microscopists,
We have recentlyacquired a scanning electron microscope with
a
four crystal WavelengthDispersive Spectrometer but the
associated
computer system is rather old andprobably not worth
re-activating.
I know that there is software for theMacintosh, such as
"D.T.S.A." and "Flame", for ENERGY Dispersive Spectroscopybut my
question
is "Is there any (Mac) software out there which can
handleW(AVELENGTH)DS
spectral acquisition and processing?".
Any leads would bevery much appreciated. Thanks.
Rick Hall
Materials ScienceProgram
University of Delaware
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From: Not Specified: Kris_Kavanau-at-dmcmail.ucsf.edu Date: Fri,03
Feb 1995 10:03:40 PST
Subject: Uranyl Glass/FM Stds. Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Reply to: RE} Uranyl Glass/FM Stds.
HiKris,
Uranium glass slides can be purchased from:
Newport IndustrialGlass, Inc.
1631 Monrovia Ave.
Costa Mesa, CA 92627
Tel: 714-642-9980
Fax: 714-645-6800
Contact person: Bill Larsen (you can tell him I sentyou).
Sold as a 6.5x6.5" sheet (you can specify 1 mm height), so you may
wantto form
a "consortium" to have Newport pre-cut a sheet to slide size
(nominalextra
cost, but your lab only needs one or two slides). If there is a
lotof
interest, my company may start selling single slides.
As forreferences and the Shading Correction equation: please see my
article in
the11/94 issue of Journal of NIH Research 6(11): 80 (usual
Internet
disclaimer:yes, that is an ad from my company on the facing page).
Also look
at Jericevicet al (1989) Methods in Cell Biology 30:47-83.
MutliSpeck beads: TheMolecular Probes pre-mounted slide kits should
be ideal
for DAPI and
Fluorescein. I believe they were optimized for Rhodamine,
but
should still workok for Texas Red. If your problem is with
mounting, Mol.
Probes now sells thebeads in solution, so you can 'sprinkle' some
on your
specimens. If you have adifferent problem with the current
MultiSpeck's, Mol.
Probes may be able towork something out for you.
Sorry, but I usually buy my reference materialfrom Mol. Probes and
don't keep
close track of other slidemanufacturers.
Sincerely,
Dr. George McNamara
Universal ImagingCorporation
George_M-at-Image1.com
--------------------------------------
Subject: Time: 9:45AM
OFFICE MEMO Uranyl Glass/FM Stds. Date:2/3/95
Dear Microscopists,
Does anyone have any uranyl glass, or know whereit might be
obtained? I
have been told that it is no longer manufacturedcommercially. It
might be
an excellent "generic" fluorescence microscopy
control.
Are there any commercially available, pre-mounted
fluorescencestandards
besides "MultiSpeck" from Molecular Probes? They are
veryconvenient, but
they are not ideal for our applications as DAPI, fluorescein,and
Texas Red
specific controls. Unfortunately, Flow Cytometry Standards Co.no
longer
makes pre-mounted standards.
I have been managing the UCSF coreflow and image cytometry facility
("Lab
for Cell Analysis") for 2 years, but Ihad no real QC for our
2
occasionally used fluorescence microscopes. Now Ineed to establish
QC
protocols for 6 additional multi-user, computerizedfluorescence
(one
scanning confocal) microscopes in the "National
MolecularCytogenetics
Resource." I was surprised that so few standards (and
journalreferences)
seem to be available.
Any suggestions or comments would begreatly appreciated. Thank you
very
much. KrisKavanau; kavanau-at-dmc.ucsf.edu
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From: SiSTek-at-aol.com Date: Mon, 6 Feb 1995 13:53:07 -0500
Subject: subscribe Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Subscribe, please.
Thanks,
Mark Anderson,
SiSTek
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From: Deborah Holmberg: dlholmberg-at-ucdavis.edu Date: Mon, 6
Feb1995 11:01:33 -0800 (PST)
Subject: Scanning 95 meeting Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
The organizers of the 28-31 March 1995 Scanning 95 meetingwant
about 25
student volunteers to run the slide projectors for the
sessionsin
exchange for full meeting registration ($275). Please
contact:
Mary K.Sullivan
FAMS, Inc
P.O. Box 832
Mahwah, New Jersy
07430,0832
or leave me a message.
Debe Holmberg e-mail {dlholmberg-at-peseta.ucdavis.edu}
Lab 916-752-9021
FAX 916-752-4604
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From: David Leaffer(415)852-1828 : David.Leaffer-at-syntex.com
Date: 06 Feb 1995 11:56:02 -0800 (PST)
Subject: TEM Calibration Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Return-receipt-to: David.Leaffer-at-syntex.com
Registered-mail-reply-requested-by:
David.Leaffer-at-syntex.com
I am going to beworking on an TEM project that will be under "GLP"
. GLP are
guidlines fordoing certain experiments for the FDA (I think the
equivalent in
Europe is ISO9000). I was wondering if anyone out there is doing
TEM under
these guidlines?And if so what are they using for magnification
calibration.
I do not believethat there are any vendors who can supply a
certified
magnification standardfor TEM, which, I think is required for
GLP.
Thanks,
DavidLeaffer
Syntex Research
david.leaffer-at-syntex.com
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From: Deborah Holmberg: dlholmberg-at-ucdavis.edu Date: Mon, 6
Feb1995 16:38:54 -0800 (PST)
Subject: Scanning 95 meeting Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
The organizers of the 28-31 March 1995 Scanning 95 meetingwant
about 25
student volunteers to run the slide projectors for the
sessionsin
exchange for full meeting registration ($275). Please
contact:
Mrs.Mary K. Sullivan
FAMS. Inc.
P.O. Box 832
Mahwah, NJ 07430-0832
or leave me a message.
Debe Holmberg
Lab 916-752-9021
Fax 916-752-4604
dlholmberg-at-peseta.ucdavis.edu
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From: richard.easingwood-at-stonebow.otago.ac.nz (Richard
Easingwood) Date: Wed, 8 Feb 1995 13:50:28+1100
Subject: Academic role Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Dear All,
We are are multi-user electron microscopefacility which has an
extensive
range of equipment and uses a wide range oftechniques.
Five technical staff from three contributing University
departmentsare
employed full-time to undertake for work coming from both
insideand
outside the University.
The role of the 'academic in charge' of thefacility is shortly to
come up
for reassessment and so it is a pertinent timefor us to reconsider
what
that role should entail.
We are looking forfeedback from other individuals as to what they
see the
contribution of anacademic in this environment should be.
Any opinions/suggestions?
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From: Nestor J. Zaluzec-Argonne Nat. Lab. :
ZALUZEC-at-AAEM.AMC.ANL.GOV Date: Tue, 7 Feb 1995 21:59:52 -0600
(CST)
Subject: Post Doc InTribology ContentsRetrieved from Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
From: wabutter-at-ix.netcom.com (Wayne A. Buttermore) Date: Tue, 7
Feb 1995 20:03:15 -0800
Subject: subscribe Contents Retrieved from Microscopy Listserver
Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {9502071626.AA16923-at-riker.ml.wpafb.af.mil}
Subscribe
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From: Peter Goodhew: goodhew-at-liverpool.ac.uk Date: Wed, 8
Feb1995 08:43:25 GMT
Subject: Re: Academic role Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
} The role of the 'academic in charge' of thefacility is shortly to
come up
} for reassessment and so it is a pertinenttime for us to
reconsider what
} that role should entail.
} We are lookingfor feedback from other individuals as to what they
see the
} contribution ofan academic in this environment should be.
Easy -
1. Keep abreast of alltechniques which a) you have, b) exist, and
c) potentially exist.
2. Be anexpert practionioner of two or more of these. Publish a lot
in your ownname.
3. Give advice on the application of all techniques and on the
high-levelinterpretation of all results. Publish
jointly with others.
4. Raise fundsto replace equipment and to buy new techniques as
they become applicable.
5.Make sure all users publish, and tell you about it!
6. Establish a reputationas a scientist in some major subject area,
not just as a microscopist. Publish alot.
7. Keep friendly with the heads (or budget controllers) of all
potential
user departments.
8. Get to know lots of people in your institution by
playingsport/drinking/etc with them.
9. In your spare time, publish somemore.
I offer this advice after 20 years of running such afacility!
PeterGoodhew
----------------------------------------------------------------------------------------------------------
Professor Peter J Goodhew,Department of Materials Science &
Engineering
University of Liverpool
LIVERPOOL Fax (44) (0)51 794 4675
L69 3BX, UKTel (44) (0)51 794 4665 (secretaryDebra)
----------------------------------------------------------------------------------------------------------
inter alia: Director of the MATTER projectfor
educationalsoftware
----------------------------------------------------------------------
------------------------------------
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From: Philip.P.Edge-at-ioppl.co.uk (Tel 0272 297481) Date: Wed, 8
Feb 1995 11:11:01 +0000
Subject: Subscribe Contents Retrieved from Microscopy Listserver
Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
X400-Received: by /PRMD=pipex/ADMD=pipex/C=gb/; Relayed; Wed, 8
Feb 1995 11:15:19 +0000
X400-Received: by mta relay1.pipex.net
in/PRMD=pipex/ADMD=pipex/C=gb/; Relayed; Wed, 8 Feb 1995 11:15:19
+0000
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11:11:01 +0000
subscribe
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From: Philip.P.Edge-at-ioppl.co.uk (Tel 0272 297481) Date: Wed, 8
Feb 1995 11:14:29 +0000
Subject: Bioimaging Contents Retrieved from Microscopy Listserver
Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
X400-Received: by /PRMD=pipex/ADMD=pipex/C=gb/; Relayed; Wed, 8
Feb 1995 11:18:34 +0000
X400-Received: by mta relay1.pipex.net
in/PRMD=pipex/ADMD=pipex/C=gb/; Relayed; Wed, 8 Feb 1995 11:18:34
+0000
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Relayed; Wed, 8 Feb 199511:14:42 +0000
X400-Received: by /PRMD=iopp/ADMD=0/C=GB/; Relayed; Wed, 8 Feb1995
11:14:29 +0000
Institute of Physics Publishing
Techno House Tel: +44 272 297481
RedcliffeWay Fax: +44 272 294318
Bristol
BS1 6NX England Telex: 449149 INSTPG
E-mail Contact Details
----------------------
Internet :{mailbox} -at-ioppublishing.co.uk
Janet : {mailbox} -at-uk.co.ioppublishing
X400 : /s= {mailbox}/o=ioppl/prmd=iopp/admd=0/c=gb/
IOPP Internetservices
----------------------
Gopher : gopher.ioppublishing.com
WWW
Url : http://www.ioppublishing.com
Dear Moderator
I am thePublisher of the journal Bioimaging which I hope you have
heard
of. I wouldlike to place information about the journal, including
tables
of contents, onyour bulletin board. Will this be possible and how
should I
do it?
Bestwishes, Philip Edge.
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From: jester-at-crnjjsgi.swmed.edu (James V. Jester) Date: Wed, 08
Feb 1995 12:10:01 -0600
Subject: Lab Design Contents Retrieved from Microscopy Listserver
Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Several years ago there appeared an article in
Science discussing
laboratory space design and a recent "New" model beingimplemented
in
England. Does anyone remember this article, and what
hashappened
to the English experiment?
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From: Marc Brande: brande-at-sdsc.edu Date: Wed, 8 Feb 199510:04:15
-0800 (PST)
Subject: Timelapse Cell Culture Movies Contents Retrieved
fromMicroscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Microscopy List {microscopy-at-aaem.amc.anl.gov} ,
Functional Neuroimaging List {lat-at-po.cwru.edu} ,
ConfocalMicroscopy List {confocal-at-ubvm.bitnet} ,
Cell Bio List {cellbiol-at-net.bio.net}
Message-Id:
{Pine.3.05.1.9502081015.B14211-a100000-at-pauline.sdsc.edu}
Mime-Version: 1.0
Content-Type: TEXT/PLAIN; charset=US-ASCII
Can Anyone point me to sources (free to minimal cost) of analog
(VCRtape)
or digital timelapse movies of cells in culture? This is
notfor
commercial use, only presentation demonstration. Of course I
wouldcredit
each source in the presentation. Thanks in advance for any help you
cangive.
Marc
Marc C. Brande, M.S. SD3D Email List:3D Imaging
San Diego 3D Imaging Group To
subscribe/unsubscribe:listserv-at-bobcat.etsu.edu
3840 Camino Lindo To post a message:sd3d-at-bobcat.etsu.edu
San Diego, CA 92122 Email:BRANDE-at-SDSC.EDU
Voice:619-587-4830
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From: evansnd-at-ornl.gov(Neal D. Evans) Date: Wed, 8 Feb 1995
13:17:21 -0500
Subject: Subscribe Contents Retrieved fromMicroscopy Listserver
Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Subscribe Microscopy evansnd-at-ornl.gov
Dr. Neal
D. Evans
Shared Research Equipment Program
Oak Ridge NationalLaboratory
Building 5500, MS 6376, Oak Ridge, TN 37831-6376
voice(615-576-4427) fax(615-574-0641)
email(evansnd-at-ornl.gov
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From: stuw-at-lanl.gov(Stuart Wright) Date: Wed, 8 Feb 1995
11:22:29 -0700
Subject:Reconditioned #SEMs Contents Retrieved from Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {9502081818.AA09732-at-mustang.mst6.lanl.gov}
X-Sender: stuw-at-mustang.mst6.lanl.gov
Mime-Version: 1.0
Content-Type:text/plain; charset="us-ascii"
Is anyone aware of a company that sellsreconditionedSEMs?
+---------------------------------------------------------+
|Stuart Wright Los Alamos National Lab, MST-6 |
|.........................................................|
| Mail StopG770 phone: (505) 665-3647 |
| Los Alamos, NM 87545 fax:(505) 667-5268 |
+---------------------------------------------------------+
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From: Daniel E. Sampson: des-at-rupture.ucsc.edu Date: Wed, 8
Feb1995 11:22:29 -0700
Subject: Reconditioned SEMs Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Is anyone aware of a company that sells reconditionedSEMs?
+---------------------------------------------------------+
|Stuart Wright Los Alamos National Lab, MST-6 |
|.........................................................|
| Mail StopG770 phone: (505) 665-3647 |
| Los Alamos, NM 87545 fax:(505) 667-5268 |
+---------------------------------------------------------+
------ Forwarded message ends here ------
*******************************************************************
Daniel E. Sampson dsampson-at-earthsci.ucsc.edu
Instrumentation Specialist Phone: (408) 459-4992
Earth Sciences FAX: (408) 459-3074
University of California
Santa Cruz, CA
95064
*******************************************************************
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From: Elinor Solit: cambrex-at-world.std.com Date: Wed, 8 Feb1995
17:34:11 +0001 (EST)
Subject: Re: Reconditioned #SEMs Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Stuart,
Have you tried contacting the instrumentmanufacturers themslves?
I
believe that JEOL and Hitachi, for instance, maysell the
reconditioned SEMs that comes in on trade-ins. Failing that,
give
us a call, we'll try to direct you to more sources.
Ellie Solit,
Publisher of MICROSCOPE TECHNOLOGY & NEWS AND
THE MICROSCOPEBOOK
On Wed, 8 Feb 1995, Stuart Wright wrote:
} Is anyone awareof a company that sells reconditioned SEMs?
}
}
}+---------------------------------------------------------+
} | Stuart WrightLos Alamos National Lab, MST-6 |
}|.........................................................|
} | Mail Stop G770phone: (505) 665-3647 |
} | Los Alamos, NM 87545 fax: (505)667-5268 |
}+---------------------------------------------------------+
}
}
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From: richard.easingwood-at-stonebow.otago.ac.nz (Richard
Easingwood) Date: Thu, 9 Feb 1995 16:43:19+1100
Subject: Academic role Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {199502090437.RAA16024-at-arwen.otago.ac.nz}
X-Sender: st004718-at-brandywine.otago.ac.nz
Mime-Version: 1.0
Content-Type: text/plain; charset="us-ascii"
Dear All,
Further to my message of8.2.95, thank you very much to those who
have
responded so candidly to myrequest for people's feelings and
experiences
on this topic. I appreciate thatit can be a sensitive issue, not
helped
when one is replying to someone whodoesn't even identify
themselves
properly.
As I neglected to state who I amand where I work (I changed
computers days
ago and forgot to put the automaticsignature on - the ramifications
of
this I am just becoming aware of...) thatinfo now follows.
Maybe now I'll get some more replies...
RichardEasingwood
South Campus Electron Microscope Unit
Otago Medical School
POBox 913
Dunedin
NEW ZEALAND
Telephone: 64-03-479 7301
Facsimile:64-03-479 7254
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From: Kathy Walters: kwalters-at-emiris.iaf.uiowa.edu Date: Thu,9
Feb 1995 07:17:27 -0600 (CST)
Subject: Neg stain of lipids Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Dear Fellow Microscopists,
I have been asked to doparticle sizing of a 10% fat immulsion (pH
8.0)
and had hoped to be able to doa very quick negative staining
procedure as
this may need to be run frequently.I toyed with the idea of
freeze
fracture, but the time involved is notconvenient for lots of runs.
Has
anyone tried this? What stains would yousuggest? Is Osmium
vaper fixation nessecary?
Thanks for anyhelp!
Kathy Walters
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From: stuw-at-lanl.gov(Stuart Wright) Date: Thu, 9 Feb 1995
09:06:22 -0700
Subject:reconditioned SEMs Contents Retrieved from Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {199502091342.AA01519-at-mail.mmmg.com}
Is
anyone aware of a company that sells reconditionedSEMs?
+---------------------------------------------------------+
| Stuart Wright Los Alamos National Lab, MST-6 |
|.........................................................|
| Mail StopG770 phone: (505) 665-3647 |
| Los Alamos, NM 87545 fax:(505) 667-5268 |
+---------------------------------------------------------+
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From: Jay Jerome: jjerome-at-isnet.is.wfu.edu Date: Thu, 9 Feb1995
11:10:54 -0500 (EST)
Subject: Re: Neg stain of lipids Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
We have considerable experience with negative stain
ofphospholipid
vesicles, lipoproteins, and triacylglyceride emulsions. In
these
circumstances fixation is not critical, and in fact can
produce
artefacts.PTA stain seems to work best. We concentrate our sample
on
grid by dryingmultiple drops under gentle nitrogen gas stream prior
to
negative stain. Thisavoids clumping in the suspension. Some
sizing
artefacts can occur as dryedparticles of large size can deform
slightly.
See Ganz et al, 1991, J Lipid Res31:163 for nice discussion of
this.
Good luck-
JayJerome
**************************************************************
* aka:W. Gray Jerome *
* Dept. of Pathology*
* Bowman Gray School of Medicine of Wake Forest University *
* MedicalCenter Blvd *
* Winston-Salem, NC 27157-1092 *
* 910-716-4972
*
* jjerome-at-isnet.is.wfu.edu*
**************************************************************
On Thu,9 Feb 1995, Kathy Walters wrote:
} Dear Fellow Microscopists,
}
}I have been asked to do particle sizing of a 10% fat immulsion (pH
8.0)
} andhad hoped to be able to do a very quick negative staining
procedure as
} thismay need to be run frequently. I toyed with the idea of
freeze
} fracture,but the time involved is not convenient for lots of
runs. Has
} anyone triedthis? What stains would you suggest? Is Osmium
} vaper fixationnessecary?
}
} Thanks for any help!
} Kathy Walters
}
}
}
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From: tivol-at-tethys.ph.albany.edu Date: Thu, 09 Feb 1995 12:06:33
EST
Subject: Re:Neg stain of lipids Contents Retrieved from Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Dear Kathy,
Staining is not really my field, but I'd
suggest a water-soluble heavy
metal and NO osmium. The Os would only dissolvein the lipid and
reduce con-
trast. If possible, looking at a frozen, hydrated(or lyophyllized
in-situ)
specimen would be best. You don't specify either thematrix of the
emulsion
(I assume aqueous) nor the technique to be used (Iassume TEM), but
a possible
protocol would be to add the stain to the emulsionand rapidly
freeze, then
cryo-section, examine on a Friday, raise the temp to~-90C, come in
Saturday
and raise the temp to -80C, Sunday to -70C, and look atthe
freeze-dried spec-
imen Monday. If you can do the particle sizing from
thefrozen-hydrated spec-
imen, the last steps can be omitted. Keeping the stainstrictly in
the aqueous
phase should prevent size changes, etc. in the lipiddrops. Good
luck.
Yours,
BillTivol
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From: jacobb-at-ux5.lbl.gov Date: Thu, 9 Feb 1995 13:50:06
-0800
Subject: Re: Reconditioned SEMs Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Stuart,
E.J. Fjeld Co,
3 Executive Park
Drive
North Billerica MA 01862
Phone 508-667-1416
Providesreconditioned AMRAY microscopes. They also make special
stages and
accessories.They've been around for a long time and are
reliable.
Jacob Bastacky,MD
1-116
Lawrence Berkeley Laboratory EMail: sjbastacky-at-lbl.gov
University of California Phone: (510) 486-4606
Berkeley, California 94720 Fax: (510) 486-4750
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From: Elinor Solit: cambrex-at-world.std.com Date: Thu, 9 Feb1995
15:20:13 +0001 (EST)
Subject: Re: reconditioned SEMs Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Stuart, my attempts to reply to your question by email haveresulted
in 6
notices of undelivered mail. I left a voice message on yourphone
this
morning. I think we can help you in yoursearch.
Regards,
Ellie Solit, Publisher/Executive Editor of MicroscopeTechnology
& News
and The Microscope Book, a Smart catalog.
On Thu,9 Feb 1995, Stuart Wright wrote:
} Is anyone aware of a company that sellsreconditioned SEMs?
}
}
}
}+---------------------------------------------------------+
} | Stuart WrightLos Alamos National Lab, MST-6 |
}|.........................................................|
} | Mail Stop G770phone: (505) 665-3647 |
} | Los Alamos, NM 87545 fax: (505)667-5268 |
}+---------------------------------------------------------+
}
}
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From: Jean Armour Polly: jpolly-at-nysernet.ORG Date: Thu, 9 Feb
199513:00:28 -0500
Subject: Apple QuickTime Conferencing Contents Retrieved from
Microscopy ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-ID:
{95020916094142E.RQDA-at-USCN.USCN.UGA.EDU}(UMass-Mailer
4.04)
Neuroscience List {neur-sci-at-net.bio.net} ,
Microscopy List {microscopy-at-aaem.amc.anl.gov} ,
Digital Video List{digvid-l-at-ucdavis.edu} ,
Confocal Microscopy List {confocal-at-ubvm.bitnet} ,
Cell Bio List {cellbiol-at-net.bio.net}
Message-Id:{Pine.3.05.1.9502091131.A22203-e100000-at-pauline.sdsc.edu}
Mime-Version:1.0
Content-Type: TEXT/PLAIN; charset=US-ASCII
I thought this postshould be quickly disseminated.
Marc C. Brande, M.S. SD3D EmailList:3D Imaging
San Diego 3D Imaging Group To
subscribe/unsubscribe:listserv-at-bobcat.etsu.edu
3840 Camino Lindo To post a message:sd3d-at-bobcat.etsu.edu
San Diego, CA 92122
Email:BRANDE-at-SDSC.EDUVoice:619-587-4830
---------- Forwarded message ----------
THEFOLLOWING RELEASE MOVED OVER PR NEWSWIRE ON TUESDAY, FEBRUARY 7,
1995 AT
11:42
AM, PST.
Contact:
Julie Karbo
Stirling & Cohan
(415) 513-0974
e-mail: jkarbo-at-applelink.apple.com
Brooke Cohan
Stirling &Cohan
(415) 513-0973
e-mail:cohan-at-applelink.apple.com
AppleAnnounces QuickTime Conferencing
Open, Cross Platform Conferencing,Collaboration and
Multimedia
Communications Technology
SAN FRANCISCO,California--February 7, 1995--Apple Computer
today
announced a cross platformconferencing, collaboration and
multimedia communications technology thatallows personal
computer
users to share real-time information, images and soundanywhere
in
the world. Apple is currently making the technology,called
QuickTime Conferencing, available to corporate allies who
planto
create or have announced they are creating end user
applications
based onthe technology. QuickTime Conferencing is a
standards-
based architecture thatallows users to:
-- video conference and collaborate--to share and annotate
text,
images, screen capture, sound, video and virtual scenes
real-time
among fellow conference participants in a variety oflocations
worldwide. QuickTime Conferencing allows users torecord
conversations and transform those conversations intoQuickTime
movies. All of this can be done on a variety of networks
suchas
an Integrated Services Digital Network (ISDN), the worldwide
internet,local area and wide area networks and Asynchronous
Transfer Mode (ATM)networks. QuickTime Conferencing can be
used
by a number of simultaneoususers, the total number being only
by
available network bandwidth.
--conduct cross platform video conferencing connectivity
between Macintoshcomputers, PCs, UNIX systems and room-based
conferencing systems through theuse of the H.320 worldwide
teleconferencing standard.
-- broadcast andview multimedia content--digital audio, music
and video on a local or wide area
network.
Through alliances QuickTime Conferencing technology is
expectedto
yield product bundles such as:
-- Apple Media Conference Kit--Consistingof the QuickTime
Conferencing system extension, the Apple MediaConference
application and a high quality, color video camera.
-- AppleMedia Conference Pro Kit--Consisting of the QuickTime
Conferencing systemextension, the Apple Media Conference
application, a color video camera and anH.320 codec/ISDN
adapter
board. Being developed by Sagem/SAT, a leadinginternational
communications product company, the board is designed toallow
interoperability between platforms (Power Macintosh to
Macintosh,
PC,UNIX and room systems) and full-screen image sharing.
--Complete MediaConference System--Consisting of an Apple
Media
Conference Kit, a Power
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Macintosh 7100 AV, a 17 inch color
monitor, external speakers and akeyboard.
Because QuickTime Conferencing is software-based, it iseasily
incorporated into new and existing third party products.
Assuch,
Apple believes that QuickTime-compatible products couldyield
extremely affordable prices:
-- Apple Media Conference Kit--under$200
-- Apple Media Conference Pro Kit--under $1,750
-- Complete MediaConferencing System--under $6,000
Apple is working with a wide range ofcompanies including
telcos,
network, software and hardware providers and
developers to provide
a range of solutions that take advantage of the benefitsof
QuickTime Conferencing (see associated releases). These
allies
haveannounced that they expect to make products available in
the
second quarter of1995.
From the home office to university campuses to
themultinational
enterprise network, QuickTime Conferencing will allow usersto
communicate with people across the country or across the
world.
Userswon't have to worry about whether their hardware
equipment,
networkingequipment and applications are compatible with the
solutions being used on theother end of the network line.
QuickTime Conferencing is designed to be fullyoperational
with
H.320 standards-based systems.
"The introduction ofQuickTime Conferencing will not only
extend
Apple's leadership in multimedia,but will make an important
difference in the video conferencing andcollaboration
market,"
said Rick Shriner, vice president of Apple's Core
Technologies
Group. "Our goal in designing QuickTime Conferencing wasto
develop a solution that allowed people the opportunity to
communicate andcollaborate. By making it open in every sense
of
the word, our users canmetaphorically break down the walls of
their homes, schools and offices andexpand the boundaries of
their lives."
QuickTime Conferencing users canhave access to people,
information, sights and sounds that could never becombined
before. For example:
-- An author in Tokyo, Japan and herpublisher in San
Francisco,
California can view and discuss cover art for a newnovel.
They
can each view the design at several different angles,change
the visual perspective of the artwork, and annotate the
imageand
accompanying text for the other to see.
-- A sixth grade class inDallas, Texas can discuss and view
the
effects of global warming with anenvironmental scientist at
U.C.
Berkeley's Lawrence Labs in California by using
QuickTime
Conferencing over the internet.
-- A special effects producer inHollywood, California can take
a
movie director on the East Coast through avirtual tour of a
proposed set design. While the producer records
theirdiscussion
as a QuickTime movie, the director can pan around the
scene,zoom
in to look at props and view the set design from a varietyof
angles.
-- A breast cancer patient and her doctor in Fargo,
NorthDakota
can consult with a leading oncologist in Boston, Massachusetts
on
herprognosis and course of treatment. The Boston physician
can
view hermammograms and annotate her medical chart as they
converse.
-- A CEO'scompany-wide address can be broadcast for easy
viewing
by all employees attheir personal desktop.
Because QuickTime Conferencing allows for sharingof
multimedia
data and reduces the time and expense of travel, it
allowspeople
to be more productive than ever before.
"In the past people found
video conferencing easy to resist
because prices were high and the number ofpeople they could
communicate with was extremely limited," said RickLeFaivre,
senior vice president of the Apple Technology Group. "Nowfor
what we expect to be very aggressive prices, people can conduct
a
mediaconference with virtually anyone, anywhere in the world.
A
Power MacintoshQuickTime Conferencing user can share QuickTime
VR
(virtual reality) images,annotate text documents and share
digital
music over networks from basic rateISDN to the internet to
ATM."
Because QuickTime Conferencing is a software-based
architecture,
application developers, communications providers andhardware
vendors can easily develop compatible solutions. Forexample,
Crosswise Corporation, the maker of Face to Face, a cross-
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platform
document conferencing application, developed aQuickTime
Conferencing-compatible version of their software in justone
month. A QuickTime Conferencing compatible application
sharesthe
interface of other QuickTime Conferencing-enabled thirdparty
applications, so customers can begin using applications
quickly
andeasily.
QuickTime Conferencing is based on Apple's award
winningQuickTime
technology. It is a conferencing architecture whichallows
support for both industry standards such as H.320, as well
as
proprietary architectures, and codecs such as Indeo by Intel
Corporation.QuickTime Conferencing is transport, compression
and
media-device independent.Apple's built-in AV capabilities
combined with the performance of the PowerPCRISC
architecture,
make it easy for users to make multimedia connections
withothers
on the information superhighway almost as soon as they pull
QuickTimeConferencing out of the box.
"Having QuickTime Conferencing available in myhome, office,
and
studio literally allows me to be in multiple locations atone
time--it's the next best thing to having a Star Trek
transporter,"
saidLos Angeles-based screenwriter and multimedia special
effects
consultantMichael Backes, co-author of the screenplay for
Jurassic Park and other motionpictures. "Within the next few
months, I'll be counting on QuickTimeConferencing as the
backbone
for my business."
"The short and sweet ofQuickTime Conferencing is that it
requires
less network bandwidth and uses
innovative technology," says Matt
Ghourdjian, National Director of Technologyat Howrey & Simon,
a
300-lawyer law firm serving Fortune 50 clients. Howrey
&Simon
intends to use the product to send QuickTime movies of
depositions
andre-enactments for lawyers to use in court; for live document
sharing;
forconsultation between partners; and to conduct tours of the
firm's
Washington,DC office from Los Angeles. "It's simply outstanding,"
says
Chris Masten,Howrey & Simon's Technical Litigation Support
Manager.
To use the AppleMedia Conference Kit on the Macintosh, users
need
at least 16 Megabytes of RAM,a 68040 or PowerPC-based
Macintosh,
System 7.5, a network interface such asEthernet, ISDN, Token
Ring, and optionally the ability to digitize audio andvideo
using
the built-in AV subsystem or a third party digitizer card.
Touse
the Apple Media Conference Pro Kit on Macintosh, users need
at
least 16Megabytes of RAM, an AV PowerPC-based Macintosh and
an
ISDN connection. To
communicate with QuickTime Conferencing users
from the PC and other platforms,users will need an H.320
compatible codec on their machine, available from avariety of
vendors. QuickTime Conferencing technology is currentlyunder
development and products using the technology have not
yetbeen
completed. Apple will provide pricing and availability
informationwhen products are completed and ready for release.
Apple Computer, Inc., arecognized pioneer and innovator in
the
information industry, creates powerfulsolutions based on easy
to
use personal computers, servers, peripherals,software, online
services, and personal digital assistants. Headquarteredin
Cupertino, California, Apple (NASDAQ:AAPL)
develops,manufactures,
licenses and markets products, technologies and services
forthe
business, education, consumer, scientific & engineering
and
governmentmarkets in over 140 countries.
-30-
Apple, the Apple logo,
QuickTime and Macintosh are registered
trademarks and Power Macintosh is atrademark of Apple
Computer,
Inc. Additional company and product names may betrademarks or
registered trademarks of the individual companies andare
respectfully acknowledged.
END
Applelink pathway:
NewsBreak
Apple & Industry News
PR Express
Apple PressReleases
2/7/95
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From: Dascorr-at-aol.com Date: Fri, 10 Feb 1995 10:38:26
-0500
Subject: Reconditioned SEMs Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
I know of a company that reconditions old AMRAY SEMs. The
owner used to work
at AMRAY before starting his own company. Company is E.J.Feld
located in
Massachusetts. I can give you the phone on Monday, 2/13 when
Ireturn to
work.
Dr. David A. Shifler
Powell Labs Ltd.
Baltimore, MD31231
(410) 327-3500
(410) 327-7506 (FAX)
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From: Liang, Long: LLIANG-at-is.Arco.COM Date: 10 Feb 199511:07:11
CST
Subject: Books-- EM & Geology ? Contents Retrieved from
Microscopy ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id:
{MACMS.LLIANG.061405110095041FMACMS-at-IS.ARCO.COM}
Dear Microscopists,
Does anyone know if there isany recent books about applications
of
microbeam techniques to mineralogy andpetrology?
The one I have was published by Mineralogical Association
ofCanada
(Short Course in Microbeam Techniques) in May 1976.
Thanks inadvance.
Long LIang
ARCO EPMA/SEM Lab
PLano, TX
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From: JoRita Jordan: jjordan-at-world.std.com Date: Fri, 10 Feb1995
13:27:19 +0001 (EST)
Subject: TEM comments sought Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
TEM users:
Thanks to all the replies to my recentTEM survey, I am well on my
way to
preparing the survey for publication. I needsome information -- I'm
a
chemist, not a microscopist -- What do TEM users seeas important
trends in
TEM? New technology? Important applications? Is thereother
technology that
is replacing TEM in any way. How important areaccessories like EDS
and
EELS? For what uses?
Any comments on today'sTEM would be greatly appreciated -- I'll
send a copy
of the survey to anycontributor.
Jo Rita Jordan
Analytical Consumer
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From: DCROMEY-at-CCIT.ARIZONA.EDU Date: Fri, 10 Feb 1995 13:50:01
-0700 (MST)
Subject:Phone # for Presetation Technol. needed Contents Retrieved
from Microscopy ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Does anyone in the group have the phone number
forPRESENTATION
TECHNOLOGY? We are in the information gathering stage for
thepurchase
of a 35mm slide maker and the phone number we have (408-774-3733)
isnot
correct.
Thanks for your help.
Doug
Douglas W.Cromey, M.S.
Cell Biology and Anatomy
Arizona Health Sciences Center
1501 N. Campbell Ave.
Tucson, AZ 85724
(602)626-2824dcromey-at-ccit.arizona.edu
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From: Peter D. Barnett: pbarnett-at-crl.com Date: Fri, 10 Feb
199522:41:51 -0800 (PST)
Subject: Phone # for Presetation Technol. needed Contents Retrieved
fromMicroscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
help
Peter D. Barnett - Forensic Science Associates- Richmond CA
pbarnett-at-crl.com VOICE: 510-222-8883 FAX: 510-222-8887
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From: timonf-at-earth.ruu.nl(Timon Fliervoet) Date: Mon, 13 Feb
1995 08:24:35 +0100
Subject: Re:Books-- EM & Geology ? Contents Retrieved from
Microscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {n1419587852.54350-at-qmgate.anl.gov}
}
Dear Microscopists,
}
} Does anyone know if there is any recent books aboutapplications
of
} microbeam techniques to mineralogy and petrology?
}
}The one I have was published by Mineralogical Association of
Canada
} (ShortCourse in Microbeam Techniques) in May 1976.
}
} Thanks in advance.
}
} Long LIang
} ARCO EPMA/SEM Lab
} PLano, TX
Try:
McLaren,A.C., 1991, TEM of minerals and rocks, Cambridge
UniversityPress,
Cambridge
Boland, J.N. & FitzGerald, J.D. (eds), 1993, Defectsand
processes in the
solid state: geoscience applications, Developments inPetrology, Vol
14,
Elsevier, Amsterdam
Buseck, P.R. (ed), 1992, Mineralsand reactions at the atomic scale:
TEM,
Mineralogical Society of America,Reviews in Mineralogy, vol
27.
CheersTimon
------------------------------------------------
Timon Fliervoet,Timonf-at-earth.ruu.nl, Faculty of Earth Sciences,
Department
of Geology,
Utrecht University, P.O. Box 80.021 3508 TA Utrecht, the
Netherlands.
tel:++31 30 - 535054, fax: ++31 30 - 537725
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From: SiSTek-at-aol.com Date: Mon, 13 Feb 1995 09:29:32 -0500
Subject: Need TEM analysis Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Help please!! SiSTek is looking for TEM analytical services
in the
southwestern US, preferably in the Phoenix metropolitan area where
weare
located. We are a company that provides consultant services to a
numberof
manufacturers of Si-related deposition systems and need
*local*(turnaround
time and iterative analysis is important for our clients)
TEMsupport. We
believe there is a company in the Phoenix area offering
TEMservices, but
can't find the name. Does anyone know thename/contact?
Many thanks,
Mark Anderson, SiSTek
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From: ckblack-at-dow.com(U096585) Date: Tue, 14 Feb 1995 11:03:19
-0500
Subject: mycoplasm incell culture ContentsRetrieved from Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Hello folks.....
This may not be the correct forum
for the
following query, however, any info out there would
be greatlyappreciated.
We are interested in microscopy techniques,
testingprocedures, staining , etc., for detection
of mycoplasm in cellcultures.
Thankyou in advance.
Cary Black (ckblack-at-dow.com)
Dave Williams
The Dow Chemical Company
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From: Doug Davis: doug_davis-at-maillink.berkeley.edu Date: 14Feb
1995 09:05:10 -0800
Subject: Ecomet Polisher for sale Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-ID: {n1419369693.44281-at-maillink.berkeley.edu}
Subject: Time: 9:13AM
OFFICE MEMO Ecomet Polisher for sale Date:2/14/95
FOR SALE: ECOMET 1 8" Polisher/grinder, complete with
variouspolishing
discs, alumina and lapping oil. 115 volt, 5 amp, new price in
1988=
$1250.00
Best offer.
Call Doug Davis of EM Lab at UC Berkeley at(510) 642-2085
or e-mail: doug_davis-at-maillink.berkeley.edu
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From: jad1-at-cec.wustl.edu(Joe DeMaro) Date: Tue, 14 Feb 1995
12:02:43 -0600
Subject: SEM wellplates Contents Retrievedfrom Microscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Any tips on cutting wells out of 24 well cell culture
plates would be
greatly appreciated.
Joe
Joseph A.DeMaro
Washington University Medical School
Department of Neurology
660S. Euclid
Rm 212 Biotech
St. Louis, MO 63110
jad1-at-cec.wustl.edu
314-362-9448
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From: Self: SALES/GREGB Date: Thu, 9 Feb 1995 13:25:54
Subject: Re: printers for gray scale prints Contents Retrieved from
Microscopy ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Forwarded message:
All,
LaserMasterCorporation - Imaging Division is the ONLY company
that manufactures a 1800 dpiplain paper laser printers. I work
for
LaserMaster and have just completedprinting the 100/300 dpi
Round
Robin Greyscale Test images. If you areinterested in
obtaining
them, you may e:mail me at Gregb-at-Sales.LMT.com and Iwill mail
you a
printout of the test images from the LaserMaster printer. I
canbe
reached at 1-800-950-6363 Ext: 3207 if you have questions
aboutyour
specific situation and resolution needs.
Thank You all,
GregBegin - LaserMaster Corp.
Scientific/Medical Imaging Div.
/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\/\\/\/\/\/\/\/\/\/\/
} Date sent: Thu, 09 Feb 95 07:42:30 -600
} From:Supratik_Guha-at-mail.mmmg.com (SG)
} To: microscopy-at-aaem.amc.anl.gov
} Subject: printers for gray scale prints
} I
am looking around for a gray scale printer to attach with our
Gatan
} slowscan CCD image aquisition system and would appreciate
any
} suggestions. Wewould prefer not to get a dye-sub printer due to
the
} high costs ofprinting. I understand that there are 1800 dpi
laser
} printers available,could someone point out manufacturers for
these
} machines?
}
}Supratik Guha
} Senior Materials Scientist
} 3M Corporate ResearchLabs.
}
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From: NANCY SMITH: NSMITH-at-darwin.sci.csuhayward.edu Date:Tue, 14
Feb 1995 13:51:37 PSD8PDT
Subject: sem culture well Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Hello Joe:
When I want to process cells for SEM from24 well culture dishes
I
use a Bunsen burner and a scoopula (the curved metaldevice
for
scooping out dry chemicals). First, the cells are fixed as
usualwith
glutaraldehyde then washed in buffer and distilled water.
Then,
working within a fume hood and wearing a heatproof glove, the
scoopula
isheated until red then touched to the underside of the culture
dish.
The curvedmetal is about the right size for the 24 well dishes.
It
takes 2 or 3 times toheat and cut until the whole bottom is
released. Once the initial cut is madeyou need to keep the cells
wet
and this is easily done using a squirt bottleof distilled
water.
This technique does not appear to cause damage to thecells but
we
normally look at the more centrally positioned cells to avoid
any
artefacts. Hope this helps.
Nancy Smith
Cal State Hayward
nsmith-at-csuhayward.edu
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From: Eric Wang: ewang-at-u.washington.edu Date: Tue, 14 Feb1995
15:07:16 -0800 (PST)
Subject: Electron mean free path Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
X-Sender: ewang-at-hardy.u.washington.edu
Hello,everyone:
Does anyone know where I can find some reference on
measurement
of electron mean free path of different materials? The mean free
path I
mean here is the mean free path for measuring the thickness when
doing
EELS, so this includes electrons of all the energy losses rather
than one
particular energy loss. We are particularly interested in getting
the
right electron mean free path for Chrome Oxide and evaporated
Carbon.
Thanks a lot.
Eric Wang
FB-10 Roberts Hall
Univ. ofWashington
Seattle. Wa 98195
(206) 543-1514
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From: richard.easingwood-at-stonebow.otago.ac.nz (Richard
Easingwood) Date: Wed, 15 Feb 1995 16:49:15+1100
Subject: SEM well plates Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {199502150442.RAA12340-at-arwen.otago.ac.nz}
X-Sender: st004718-at-brandywine.otago.ac.nz
Mime-Version: 1.0
Content-Type: text/plain; charset="us-ascii"
)Joe,
} Subject: SEM wellplates
} Any tips on cutting wells out of 24 well cell culture plates
wouldbe greatly
} } appreciated.
} Joe
} Joseph A. DeMaro
Depending onwhat exactly it is you are doing, how about using
Thermanox
(Thermonox?)plastic slides on the bottom of the wells - they make
them
specially to fitinto the wells of 12 well plates and possibly the
24 well
ones too. They comesterilised and you just pop them into the well
before
you add medium and cellsand remove later, fix, dry etc and mount on
a
stub. The slide surfaceproperties are supposed to duplicate the
ordinary
well bottoms.
Its easierthan cutting wells out of the bottom of the trays.
Regards REasingwood
Richard Easingwood
South Campus Electron Microscope
Unit
Otago Medical School
PO Box 913
Dunedin
NEWZEALAND
Telephone: 64-03-479 7301
Facsimile: 64-03-479 7254
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From: MatlsMicrs-at-aol.com Date: Wed, 15 Feb 1995 01:11:08
-0500
Subject: Subscribe Contents Retrieved fromMicroscopy Listserver
Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Please Subscribe
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From: Rich2442-at-aol.com Date: Wed, 15 Feb 1995 02:45:32
-0500
Subject: Request to join mailinglist Contents Retrievedfrom
Microscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
I work for an OEM of scanning electron microscopes and am
interested in
keeping up with the latest technology and issues. I would liketo
subscribe
to the mailing list. Could you please let me know what I need
todo.
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From: W.L. Steffens: STEFFENS.B-at-calc.vet.uga.edu Date: Wed,
15Feb 1995 08:41:37 EST
Subject: Cell culture plates Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
We process a considerable number of cell cultures for bothSEM and
TEM,
and have found what we consider to be the ideal system. For
thispurpose,
we have our investigators culture their cells in
Leightontubes...these
are cell culture tubes with a flat bottom which holds a
long,narrow
plastic coverslip. Once the cells are attached, the medium is
replaced
with fixative, then the coverslip (which is attached to a nifty
little
handle) is removed. The plastic on the coverslip is impervious to
all
solvents used in microscopy, and can be embedded and sectioned
forTEM.
I wouldn't think of doing it any other way.
-=W.L.Steffens=-
College of Veterinary Medicine
University of Georgia
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From: Fermin, Cesar: Fermin.Cesar-at-tmc.tulane.edu Date: 15
Feb1995 09:37:10 -0600
Subject: Beseler Enlarger tune-up Contents Retrieved from
Microscopy ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
ref.: Beseler enlarger tune-up.
We have two Beselerenlarger needing adjustments. Any
information
on available service person inthe south, please remit details
directly to me. Number I called wasdisconnected!
************************************************************
*Cesar D. Fermin, Ph.D \|*|/ Fax (504) 587-7389 *
*Tulane MedicalSchool /|*|\ Answ. Mach.(504) 584-2618 *
*Pathology/SL79 \|*|/Secretary (504) 584-2436 *
*New Orleans, La 70 112 /|*|\ Lab (504) 5841*
*Fermin-at-TMC.Tulane.edu -} Director of Morphological
Services*
************************************************************
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From: dhoyle-at-tic.ab.ca(David Hoyle) Date: Wed, 15 Feb 1995
10:59:42 -0700
Subject:registration ContentsRetrieved from Microscopy Listserver
Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id: {25021509453900-at-vms2.macc.wisc.edu}
Thank you for responding so quickly to my inquiry.
I look forward toyour news letters and hope to be able to
contribute any information Ican.
Subscribe Microscopy dhoyle.tic.ab.ca
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From: Michael Cammer: cammer-at-aecom.yu.edu Date: Wed, 15 Feb1995
11:24:52 -0500 (EST)
Subject: Re: Beseler Enlarger tune-up Contents Retrieved
fromMicroscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Back around '82 or '83 I found that I had a problem with
myBesseler's
constantly slipping focus just a tiny bit. So I put pipe
clamps(those
metal rings that can be tightened of loosened with the turn a a
screw)on
the metal guides for the focus which I would tighten when
focusingthe
bellows particulalry tight.
-mc
On 15 Feb 1995, Fermin, Cesarwrote:
} ref.: Beseler enlarger tune-up.
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From: W.L. Steffens: STEFFENS.B-at-calc.vet.uga.edu Date: Wed,
15Feb 1995 13:37:13 EST
Subject: Leighton Tubes Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
For those interested, Leighton tubes for cell culture
aremanufactured by
Corning Costar and are available from Fisher Scientific
(Cat.#07-200-
367). They appear in the 95-96 catalog on page 721.
-=W.L.Steffens=-
College of Veterinary Medicine
University of Georgia
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From: tivol-at-tethys.ph.albany.edu Date: Wed, 15 Feb 1995 15:14:40
EST
Subject: Re:Electron mean free path Contents Retrieved from
Microscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Dear Eric,
If no expert in the field has a table of
the mfp's, I can fax you
tables of stopping powers for electrons in carbon,oxygen, iron
& titanium--
you have to interpolate for chromium and calculatethe mpf from
dE/dx. Good
luck.
Yours,
Bill Tivol
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From: BARBARA.HARTMAN-at-1773.220.SCHERING-PLOUGH.sprint.com Date:
Thu, 16 Feb 1995 08:42:49 -0500
Subject: FIXATION OF TESTES FOR HISTOLOGY Contents Retrieved from
Microscopy ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
GREETINGS,
DOES ANYONE KNOW OF ABETTER FIXATIVE FOR TESTES THAN BOUINS
FOR
LIGHT MICROSCOPY? WE ARE TRYING TOAVOID THE LONG RINSING REQUIRED
WITH
BOUINS.
THANK YOU!
BARBARAHARTMAN
SCHERING-PLOUGH RESEARCH
LAFAYETTE, NJ
(201) 579-4343
(201)570-4211 (FAX)
E-MAIL:
MAIL/ADMD=TELEMAIL/PRMD=SCHERING-PLOUGH/PN=BARBARA.HARTMAN/C=US/-at-SPRINT.COM
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From: SiSTek-at-aol.com Date: Thu, 16 Feb 1995 13:48:59 -0500
Subject: Need TEM / Many thanks!! Contents Retrieved fromMicroscopy
Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Many thanks to all who responded for my call for help with
locating TEM
service near us in the Phoenix metro area. As we thought, there
isan
established group in Phoenix who have been around for a few years
andwho
provide TEM services.
For anyone else who might be interested, thecompany is called
NanoTEM, Inc,
7620 E. McKellips Rd., Suite 4109, Scottsdale,Arizona 85257, phone
602 759
2808, fax 602 947 7615.
Again, manythanks for all your help.
Mark Anderson, SiSTek
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From: baskin-at-biosci.mbp.missouri.edu (Tobias Baskin) Date: Fri,
17 Feb 1995 13:47:11 -0600
Subject: TEM/formvar substitute/thin films Contents Retrieved from
Microscopy ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Greetings,
Is there something out there thatwill make a thin film that
isn't formvar? I have been using wire loops coatedwith a film of
1.2%
formvar to support my small samples during rapid freezingand
substitution.
This works fine for acetone substitution but we would like
totry
Tetrahydrafuran (THF) as a substitution medium and, alas, THF
eatsthe
formvar.
We get a formvar film on the wire loop by castingsmall
rectangles
of formvar on water and then trasfering one to a loop.
Are there other compounds that could be used to make a film
across
the loop andthat might survive THF??
Thanks for any suggestions,
Tobias Baskin
- - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -- - -
- -
___ ____ ^ ____ _____ Tobias I.Baskin
/ \ / / \ / \ / University ofMissouri
/ | / / \ / / Biological
Sciences
/___ / /__ /_____\ / /__ 109 Tucker Hall
/ / / \ ( / Columbia, MO 65211 USA
// / \ \ / voice: 314-882-0173
/ /____ /\ \____/ /_____ fax: 314-882-0123
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From: Liang, Long: LLIANG-at-is.Arco.COM Date: 17 Feb 199514:34:14
CST
Subject: Sample Prep--Steel Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id:
{MACMS.LLIANG.644426140095048FMACMS-at-IS.ARCO.COM}
Dear Microscopists,
I am trying to preparepolished sections from steel samples for
EPMA
analysis. Are there anyrecommended abrasive/size for rough
grinding,
fine grinding, rough polishing,and final polishing?
Your help is high appreciated.
LongLiang
ARCO EPMA/SEM Lab
Plano, TX
LLIANG-at-is.arco.com
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From: Doug Arrell: ARRELL-at-jrc.nl Date: Mon, 20 Feb 199508:25:04
GMT+0200
Subject: Re: Sample Prep--Steel Contents Retrieved from Microscopy
ListserverArchives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
Message-Id:
{MAILQUEUE-101.950220082504.256-at-FS-IAM-1.JRC.NL}
}
} I am trying to prepare polished sections from steelsamples for
EPMA
} analysis. Are there any recommended abrasive/size forrough
grinding,
} fine grinding, rough polishing, and finalpolishing?
I have always stuck to the simple silicon carbide paper
(insteps
from 120 to 1200 grade) and then diamond (6,3,1um) route, and
found
no problems withthat.
Doug
+------------------------------------+
| Dr DouglasArrell |
| Mechanical Performance and Joining |
| Institutefor Advanced Materials |
| 1755 ZG Petten |
|Netherlands |
| {ARRELL-at-JRC.NL}|
| Tel. (+31) 2246 5287 |
| Fax (+31) 2246 1917|
+------------------------------------+
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From: Joyce Craig: bafpjec-at-uxa.ecn.bgu.edu Date: Mon, 20 Feb1995
11:10:51 -0600 (CST)
Subject: student microscopy competition Contents Retrieved
fromMicroscopy Listserver Archives
http://www.microscopy.com/MicroscopyListserver/MicroscopyArchives.html
CALL FOR PAPERS
STUDENT COMPETITION
TO BE HELDAT
THE UNIVERSITY OF WISCONSIN
WHITEWATER, WISCONSIN
Friday, March 24,1994
AWARDS:
FIRST PLACE $100
SECOND PLACE $75
THIRD PLACE$25
Abstracts will be published in Midwest Microscopy.
Microsgraphs fromfirst place winner will be on the cover of
Midwest
Microscopy.
Studentswill be judged on written abstract, presentation, and
quality of
study.
Student competition is open to undergraduate and graduate students
and
mayinvolve any type of microscopy.
S