Hello Histonetters,
I have been contacted with a site that is looking to fill several HT positions
at their Grenville, SC lab. If interested, please contact me and I will give
you the contact information. No recruiters please!
Jerry Santiago
Email: sant...@bellsouth.net
Hi all,
I'm still looking for ideas about the best types of TEM around at the moment.
If you have recently purchased one or have been a regular user of a late model
digital TEM please share your experience with me.
regards
Steve Weston
Lab Manager
Breathe-Well Centre of Research Excellence for Chr
Amber: I find this EXTREMELY irritating when an outside institution either
writes their accession number on the label or puts another label over the top
of my hospitals labels. It is not rude to ask other hospitals to not do this;
that doesn't mean they won't do it. I will forward you my slid
I think it's pretty standard that outside institutions put their accession ID
on the front of the consult slides.
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of Amber McKenzie
Sent: Wednesday, March 19,
Would it be rude to ask other hospitals that review my slides to NOT WRITE
their accession number on the front of my slides, but instead put their
accession number on the back of my slides? Sometimes, I get slides back that
have stickers on the front under my accession number or they'll hand wr
Dear Histonet Colleagues,
I hope everyone is doing well--
We are going to be using a goat mandible model (embedded in MMA) for a project
and will need to administer tetracycline and/or calcein (others if suggested)
for histomorphometric analysis. Would anyone be kind enough to share their
know
I am out of the office until 03/21/2014.
I will be out of the office from March 18th until March 21st. I will be
checking emails periodically and will attempt to reply to your message
within 24 hours.
Thank You,
Bruce Palmatier
Market Portfolio Manager
VWR Healthcare
bruce_palmat...@vwr.com
mob
Hi Valerie,
Why would you need to remove the sucrose? I would place the frozen blocks in
room temperature fixative or buffer with one or two changes, especially if you
have OCT that needs also to thaw.
Why fixative? You may want to consider adding additional fixation if the tissue
was minimall
We have one tech who does all of the steps in EM processing, staining
etc., but we are a research lab.
Mark Elliott
Centre for Heart Lung Innovation
Vancouver, BC
Date: Wed, 19 Mar 2014 14:25:15 +
From: "Gauch, Vicki"
Subject: [Histonet] Question for Labs performing Electron Microscop
It's the same for me here. But then again, we're pure research.
Kathleen
Principal Lab Technician
Neurotoxicology Labs
Molecular Pathology Facility Core
Dept of Pharmacology & Toxicology
Rutgers, the State University of NJ
41 B Gordon Road
Piscataway, NJ 08854
(848) 445-1443
> We used to do TE
We used to do TEM at our lab. The work volume was not high and one of
histotechnologists was trained to do ALL tasks (fixation → printing the photos
of the areas selected by the pathologist).
When not doing TEM tasks, he took care of any of any of all HTL tasks for which
he was also trained.
Ren
Hi everyone,
I have been asked to post the following question regarding EM...
If you are providing EM services in your laboratory, who is performing the EM,
what is their job title and what are their job duties ( do they process, embed,
cut,stain,etc. or just certain portions ).
Any information w
Hi Histonetters!!
I hope everyone is having a great day. I wanted to put up a quick post
because I have been talking to some managers who have told me they have been
having trouble finding "the right techs" for the positions they have open in
their labs. I know it is tricky at best to find that p
We have plenty, we just use placenta, I can send you a block or two if still
needed. What's everyone else using?
Curt
-Original Message-
From: histonet-boun...@lists.utsouthwestern.edu
[mailto:histonet-boun...@lists.utsouthwestern.edu] On Behalf Of S hay
Sent: Tuesday, March 18, 2014
Hi,
I am new to Histonet. Here is my question.
We have brain samples that were fixed in 4% paraformaldehyde then placed in 30%
sucrose (cryoprotectant) prior to freezing on dry ice. These samples have been
stored at -80 for a couple of years. We want to thaw these samples then process
them to
15 matches
Mail list logo
