Dear all:

I am writing to discuss the use of rat-sourced primary antibody on rat tissue.
One concern (from Andrea Hooper's last email to me) is that the 10mg/ml IgG in normal blood will result in great background, or false-positive staining.
How do you think?

My personal opinions are:

(1) perfuse the rat well.
(2) use a control group without 1st antibody, just add goat-anti-Rat IgG, for example (care about the cross reactivity)
(3) use DAPI staining to see if the staings are located in cell, rather by blood contamination.


2008-07-16 



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