i want to check the surface expression of a receptor in clones of a stable cell line. I just got confused if i should add antibody to my negative control? my negative control is the cell that does not express the surface receptor. And my positive control is the stable cell line that express the surface receptor.
I just confused wether i should add antibody to the negative control or should it be no stain? thank you
negative control
Started by soymilk14, Apr 05 2010 05:35 PM
3 replies to this topic
#1
Posted 05 April 2010 - 05:35 PM
#2
Posted 05 April 2010 - 07:58 PM
I would use both controls, unstained cells (cells that express the surface receptor, but no antibody) and stained cells that don't express your receptor.
#3
Posted 06 April 2010 - 04:41 PM
leelee, on Apr 6 2010, 03:58 AM, said:
I would use both controls, unstained cells (cells that express the surface receptor, but no antibody) and stained cells that don't express your receptor.
Me too. Unstained cells will allow you to set the fluorescence so they are negative and cells that don't express the receptor but have been stained with antibody will allow you to gauge how specific your antibody is as you can see how much has stuck to the cells that don't express the receptor.
#4
Posted 03 June 2010 - 07:23 PM
i will do
for both stable cell lines (expess the surface receptor or not)
1. unstain
2. isotype of the antibodies
3. the targeted antibodies
with this u will have
FCM control(unstain-detect autofluorences, isotype-specificity of the antibodies) and experimental control( +ve or negative)
this may provide enough evidence to justified the result
cheers and happy flowing
a useful link
http://hsc.usf.edu/c...ow controls.htm
thanks to flowcytometry core lab ,UNIVERSITY OF SOUTH FLORIDA for the excellent and informative webpage
for both stable cell lines (expess the surface receptor or not)
1. unstain
2. isotype of the antibodies
3. the targeted antibodies
with this u will have
FCM control(unstain-detect autofluorences, isotype-specificity of the antibodies) and experimental control( +ve or negative)
this may provide enough evidence to justified the result
cheers and happy flowing
a useful link
http://hsc.usf.edu/c...ow controls.htm
thanks to flowcytometry core lab ,UNIVERSITY OF SOUTH FLORIDA for the excellent and informative webpage














