[Histonet] negative controls
Jan Shivers
shive003 <@t> umn.edu
Fri Oct 15 16:11:47 CDT 2010
Linda,
My system of negative controls is identical to yours.
Jan Shivers
Senior Scientist
Histology/IHC/EM Section Head
Pathology Teaching Program
University of Minnesota
Veterinary Diagnostic Laboratory
1333 Gortner Ave.
St. Paul, MN 55108
612-624-7297
shive003 <@t> umn.edu
(Confidentiality Notice: This message, together with any attachments, is
intended only for the use of the individual or entity to which it is
addressed and may contain confidential or privileged information. If you
think you have received this message in error, please advise the sender and
then delete this message and any attachments immediately.)
----- Original Message -----
From: "Sebree Linda A" <LSebree <@t> uwhealth.org>
To: <sgoebel <@t> xbiotech.com>; "Rene J Buesa" <rjbuesa <@t> yahoo.com>
Cc: "Histo Net list server" <HistoNet <@t> lists.utsouthwestern.edu>
Sent: Friday, October 15, 2010 11:07 AM
Subject: RE: [Histonet] negative controls
To clarify even further: we cut 2 patient sections, put one on a slide with
a section of positive control already on it. This slide gets stained with
the antibody The other section goes on another slide and is run as a
corresponding negative control using the same antibody protocol but
substituting a negative control serum for the antibody, thus this is a
"negative reagent control" slide. Elements within the patient slide that
received antibody and are expected to be negative, serve as a "negative
tissue control". Again, we run 1 negative control slide for EVERY 1 patient
block in a run but only 1 negative control per any number of antibodies run
on that same block, using the harshest protocol. Only autopsy cases differ
in that we run 1 negative control per TISSUE TYPE.
Linda A. Sebree
University of Wisconsin Hospital & Clinics
IHC/ISH Laboratory
DB1-223 VAH
600 Highland Ave.
Madison, WI 53792
(608)265-6596
-----Original Message-----
From: sgoebel <@t> xbiotech.com [mailto:sgoebel <@t> xbiotech.com]
Sent: Friday, October 15, 2010 10:48 AM
To: Rene J Buesa
Cc: Histo Net list server; Sebree Linda A
Subject: RE: [Histonet] negative controls
So for every HP you do, you process a control cassette with the patient
tissue cassette? That seems like alot? How do you get that many
control tissues on a daily basis? What do you do with the remaining
tissue in the control block? If you throw them away everyday, I would
be interested in some of them. How do you know what IHC stains the
pathologist is going to order to know what control tissue to fix and
process at the exact same time? We have always just had a bunch of
blocks that you cut a control from? I understand that there is
variability with processing, age, etc. not trying to be dense just still
don't understand... Most places I have ever worked have control blocks
that they cut a fresh control from everyday, then stain with the patient
tissue. If there are 3 HP cases, from what I am understanding, you guys
are saying you need 3 controls for slides that are on the same machine,
with the same reagents, same antibody, and same times. Why couldn't you
just have one for all 3 cases? Then the next day have a fresh ONE for
that day, date them, and file them. So if you needed to see the HP
control for October 15th, you could go pull the control for that day...
Sarah Goebel, B.A., HT (ASCP)
Histotechnician
XBiotech USA Inc.
8201 East Riverside Dr. Bldg 4 Suite 100
Austin, Texas 78744
(512)386-5107
-------- Original Message --------
Subject: RE: [Histonet] negative controls
From: Rene J Buesa <rjbuesa <@t> yahoo.com>
Date: Fri, October 15, 2010 8:33 am
To: Sebree Linda A <LSebree <@t> uwhealth.org>, sgoebel <@t> xbiotech.com
Cc: Histo Net list server <HistoNet <@t> lists.utsouthwestern.edu>
Because each tissue block has its own characteristics regarding fixation
and processing some of which can influence the reactivity. If you have a
bank of negative controls, how can you be sure that any of those blocks
have received exactly the same treatment and reacted in the same way to
the test block?
The same goes for any bank of positives, so that is why you should have
a positive control section in the same slide as the test section.
René J.
--- On Fri, 10/15/10, sgoebel <@t> xbiotech.com <sgoebel <@t> xbiotech.com> wrote:
From: sgoebel <@t> xbiotech.com <sgoebel <@t> xbiotech.com>
Subject: RE: [Histonet] negative controls
To: "Sebree Linda A" <LSebree <@t> uwhealth.org>
Cc: "Histo Net list server" <HistoNet <@t> lists.utsouthwestern.edu>
Date: Friday, October 15, 2010, 11:17 AM
Why do you need a negative control for each block if you are runn=
ing
the same antibody on each patient block? Is it just for case by c
ase reference so the negative is filed with the patient slide? Why
co= uldn't you have a control slide bank that was dated so all
the
slides you d= id on that day, on that run, could be referenced back
to
that control? = ; Just curious?
Sarah Goebel, B.A., HT (ASCP)
Histotechnician<= br>
XBiotech USA Inc.
8201 East Riverside Dr. Bld= g 4 Suite 100
Austin, Texas 78744
=
(512)386-= 5107
-------- Original Message --------
Subject: RE: [Histonet] negative controls
From: "Sebree Linda A" <[1]LSebree@= uwhealth.org>
Date: Fri, October 15, 2010 8:08 am
To: "Victoria Baker" <[2]bakevict= oria <@t> gmail.com>, "Histo Net
list
server"
<[3]HistoNet <@t> lists.uts= outhwestern.edu>
We run negative controls on every block of a case within the same
run.
On autopsy cases, we only run 1 negative per tissue type, within the
same run...this is the only exception to the rule of 1 negative per
block.
Linda A. Sebree
University of Wisconsin Hospital & Clinics
IHC/ISH Laboratory
DB1-223 VAH
600 Highland Ave.
Madison, WI 53792
(608)265-6596
-----Original Message-----
From: [4]histonet= -bounces <@t> lists.utsouthwestern.edu
[[5]mailto:histon= et-bounces <@t> lists.utsouthwestern.edu] On Behalf
Of
Victoria
Baker
Sent: Friday, October 15, 2010 9:26 AM
To: Histo Net list server
Subject: [Histonet] negative controls
Hi
I have a hypothetical question to those who run IHC on Ventana
instruments.
Are you running your negatives with your patient/test cases or on a
separate
run? Also, if you are doing this and have to use a different
detection
kit
how do you work the QA/QC portion of this for CAP requirements.
Thanks
Vikki
_______________________________________________
Histonet mailing list
[6]Histonet <@t> lists.utsouth= western.edu
[7]http:= //lists.utsouthwestern.edu/mailman/listinfo/histonet
_______________________________________________
Histonet mailing list
[8]Histonet <@t> lists.utsouth= western.edu
[9]http:= //lists.utsouthwestern.edu/mailman/listinfo/histonet
References
1. 3D"mailto:LSebree <@t> uwhealth.org"
2. 3D"mailto:bakevictoria <@t> gmail.com"
3. 3D"mailto:HistoNet <@t> lists.utsouthwestern.edu"
4. 3D"mailto:histonet-bounces <@t> lists.utsouthwestern.edu"
5. 3D"mailto:histonet-bounces <@t> lists.utsouthwestern.edu"
6. 3D"mailto:Histonet <@t> lists.utsouthwestern.edu"
7. 3D"http://lists.utsouthwestern.edu/mailman/listinfo/histonet"
8. 3D"mailto:Histonet <@t> lists.utsouthwestern.edu"
9. 3D"http://lists.utsouthwestern.edu/mailman/listinfo/histonet"
_______________________________________________
Histonet mailing list
Histonet <@t> lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
_______________________________________________
Histonet mailing list
Histonet <@t> lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
More information about the Histonet
mailing list