The antigen doesn't decay much inside the tissue block, as long as the
sections were freshly done. We redo ER/PR on archived samples from 15 years
ago and they still stain very strongly.
Allan
On Thu, Feb 7, 2019 at 8:26 AM Heckford, Karen - SMMC-SF via Histonet <
Thanks all, looks like the consensus is that water into the clearing agent
causes it and I should change out alcohol more frequently.
Allan
On Wed, Oct 31, 2018 at 5:46 PM Allan Wang wrote:
> Hi histonet,
>
> For coverslipping Ventana IHC slides I have dish soap, rinse, alcohol 80%,
> 100%,
Hi histonet,
For coverslipping Ventana IHC slides I have dish soap, rinse, alcohol 80%,
100%, 100%, 100%, followed by three Clear-Rite 3 instead of xylene. In the
past I didn't have this issue, but now I frequently get a lot of residue on
the slides after they enter the Clear-Rite.
If I
I'd like to know as well.
Thanks,
Allan
On Thu, May 10, 2018 at 11:25 AM, Histology via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hi all,
>
> Can anyone share what type of benchtop fume hoods they are using in the
> lab? This would be for manual coverslipping and grossing.
>
>
A generator is probably the cheapest option if you can go manually start it
after a few hours.
I purchased a UPS for a DNA sequencer which shouldn't lose power when in
use. You may also want one to add a few hours of leeway before the
generator is needed.
You should measure the tissue processor's
How are labs validating for rarer biomarkers like ALK, ROS1, or MMR loss?
Following the guideline of 10 positive cases may be difficult.
I've seen other companies with control slides just with a few engineered
cell lines as positive and negative controls. Is that enough for validation
alone?
We
Hi,
We (at US Biomax) recently screened our colon TMAs for loss of expression
for MLH1, MSH2, MSH6, PMS2 using Ventana's antibodies.
If you need around 10 cases of negative tissue:
CO20813a, 208 cases of colon, contains loss of:
PMS2: 35
MLH1: 18
MSH6: 14
MSH2: 8
This TMA is not listed on our
Lysol IC as recommended by the tech and manual. I just buy the concentrated
one on Amazon and dilute it 1:250
Allan
On Mon, Jan 22, 2018 at 8:27 AM, Sharon Dwyer via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> What solution are you using to do the decontamination of the Ventana
>
Hi,
This information would be very useful for me and probably others as well,
since I've just arbitrarily chosen one.
Can you summarize the responses you received for us?
Allan
On Wed, Nov 8, 2017 at 10:28 AM, warda hassan via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hello to all
The LCS is fairly cheap in comparison to some other bulks and 650-010 is
half the price of 650-210. I don't know if there's actually any difference
between them.
I think an alternate formulation for EZ Prep (or Discovery Wash), CC1 and
especially CC2 would save more money.
Allan
On Fri, Nov 3,
Tim and Tony,
Why couldn't DAB be used on frozen sections in your example?
Allan
On Mon, Apr 17, 2017 at 9:03 PM, Tony Henwood (SCHN) via Histonet <
histonet@lists.utsouthwestern.edu> wrote:
> Hi Bianca,
> Well for most Pathology departments, Immunofluorescence (IF) is used for
> Renal and
I've found that using Clear Rite 3 instead of xylene prevented the stickers
from peeling at the bottom and producing that sticky residue. But I also
have the liquid level low to prevent direct contact.
Allan Wang
On Tue, Jan 24, 2017 at 8:53 AM, Duddey, Aimee via Histonet <
dney
> Tel: 612 9845 3306
> Fax: 612 9845 3318
> Pathology Department
> the children's hospital at westmead
> Cnr Hawkesbury Road and Hainsworth Street, Westmead
> Locked Bag 4001, Westmead NSW 2145, AUSTRALIA
>
> -Original Message-
> From: Allan Wang via Histone
Hello all,
Does someone know what would cause dirty flakes of light purple that showed
across the whole slide?
http://i.imgur.com/1nIXwAy.jpg
Reagents are relatively fresh but the H stainer hadn't been used for a
week over the holiday break.
Is it surface film on the hematoxylin? I didn't
Hello all,
I noticed CST sells most of their antibodies with 50% glycerol and
recommends -20C storage and no aliquoting. They remain in liquid form in
the freezer. A little bit more difficult to pipette precisely due to the
viscosity and temp difference, but it seems like a good trade-off for
Hello list,
I'm looking for a histotech with 2-4 years of experience, starting
immediately.
Position is at a small business which is a biorepository for cancer
researchers worldwide.
Job responsibilities:
1. Section, mount and stain very valuable tissue blocks. No tissue
processing for now.
2.
Hello list,
Thanks for your responses to my previous dehydration question. I pretty
much got conflicting responses about going straight to 100% alcohol, but I
think I will just start them out in 80% alcohol to be safe.
Something that's been bugging me: Every source states that diluted
antibodies
17 matches
Mail list logo