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
shive...@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" <lseb...@uwhealth.org>
To: <sgoe...@xbiotech.com>; "Rene J Buesa" <rjbu...@yahoo.com>
Cc: "Histo Net list server" <HistoNet@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: sgoe...@xbiotech.com [mailto:sgoe...@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 <rjbu...@yahoo.com>
Date: Fri, October 15, 2010 8:33 am
To: Sebree Linda A <lseb...@uwhealth.org>, sgoe...@xbiotech.com
Cc: Histo Net list server <HistoNet@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, sgoe...@xbiotech.com <sgoe...@xbiotech.com> wrote:


From: sgoe...@xbiotech.com <sgoe...@xbiotech.com>
Subject: RE: [Histonet] negative controls
To: "Sebree Linda A" <lseb...@uwhealth.org>
Cc: "Histo Net list server" <HistoNet@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]lseb...@= uwhealth.org>
  Date: Fri, October 15, 2010 8:08 am
  To:  "Victoria  Baker"  <[2]bakevict= o...@gmail.com>, "Histo Net
list
  server"
  <[3]histo...@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= -boun...@lists.utsouthwestern.edu
  [[5]mailto:histon=  et-boun...@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]histo...@lists.utsouth= western.edu
  [7]http:= //lists.utsouthwestern.edu/mailman/listinfo/histonet
  _______________________________________________
  Histonet mailing list
  [8]histo...@lists.utsouth= western.edu
  [9]http:= //lists.utsouthwestern.edu/mailman/listinfo/histonet

References

  1. 3D"mailto:lseb...@uwhealth.org";
  2. 3D"mailto:bakevicto...@gmail.com";
  3. 3D"mailto:HistoNet@lists.utsouthwestern.edu";
  4. 3D"mailto:histonet-boun...@lists.utsouthwestern.edu";
  5. 3D"mailto:histonet-boun...@lists.utsouthwestern.edu";
  6. 3D"mailto:Histonet@lists.utsouthwestern.edu";
  7. 3D"http://lists.utsouthwestern.edu/mailman/listinfo/histonet";
  8. 3D"mailto:Histonet@lists.utsouthwestern.edu";
  9. 3D"http://lists.utsouthwestern.edu/mailman/listinfo/histonet";
_______________________________________________
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


_______________________________________________
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet


_______________________________________________
Histonet mailing list
Histonet@lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet

Reply via email to