[Histonet] Protocol for MOM kit ( whole mount staining)
Guillermo Palao
gpbnas <@t> yahoo.es
Fri Apr 28 10:02:30 CDT 2006
In my experience trying to block deposited endogenous mouse IgG in mouse kidney from being detected with secondary anti-mouse Abs MOM kit did not work. I tried increasing concentration of blocking reagent up to 6 times what they recommended together with increased blocking times, without result. Primary Ab incubation was not important because the Ab was quite good and it worked in 1 h RT or O/N 4 ºC. Of course your level of background will depend on the amount of endogenous IgG in your mouse samples. I have now changed to rabbit mAbs with Jackson´s secondary Abs pre-adsorbed with mouse Ags.
Best regards,
Guillermo
sohail ejaz <sohail_e <@t> yahoo.com> escribió:
I am trying whole mount staining of mouse Retina, Trachea and 20 micrometer tissues with vWF (Rabbit anti human von Willibrand factor polyclonal antibody, Chemicon international) SMA (Monoclonal anti-actin, alpha smooth muscle antibody produced in mouse) and i need to use MOM kit (Vector) for this purpose.
They recommend to incubate the samples for just 30 min with primary antibody.
I wonder if this time is enough..................??
Can anyone guide me a good protocol regarding this issue.
Thanks
Dr. Sohail
---------------------------------
Love cheap thrills? Enjoy PC-to-Phone calls to 30+ countries for just 2¢/min with Yahoo! Messenger with Voice.
_______________________________________________
Histonet mailing list
Histonet <@t> lists.utsouthwestern.edu
http://lists.utsouthwestern.edu/mailman/listinfo/histonet
---------------------------------
LLama Gratis a cualquier PC del Mundo.
Llamadas a fijos y móviles desde 1 céntimo por minuto.
http://es.voice.yahoo.com
More information about the Histonet
mailing list