Hi all. I was wondering if anyone has a protocol for doing collagen gels.
I've been running 5% non reducing SDS-PAGE gels to separate type I and III
collagen from muscle tissue. I've been using a delayed reduction technique
where the dye front is run about 1/3 of the way into the separating gel,
then the power is turned off and BME added to the wells to allow the type
III collagen to migrate into the gel. My gels look great, except the type
III doesn't appear to be affected at all by the BME. The alpha and beta
chains run great, but there is a band right up near the wells that I'm
assuming is the type III. There is no visible difference between the
reduced and non-reduced lanes. Is it possible for BME to go bad? I made
everything myself, so I know there were no reducing agents in any of the
buffers etc... Has anyone else had this problem or have any suggestions?
Todd Miller, Ph.D.
University of Pennsylvania School of Medicine
Department of Microbiology
211 Johnson Pavilion
3610 Hamilton Walk
Philadelphia, PA 19104-6076
Get your FREE download of MSN Explorer at http://explorer.msn.com/intl.asp
<< Previous Message | Next Message >>