Hi,
Why it is difficult to detect the 46 Kd by vegf-b antibody? Although I
already put the sample into unreducing loading buffer (no
2-mercaethanol), run the SDS page and then electroblotting onto NC
membrane by wet method. After incubating with primary vegf-b polychonal
antibody (Santa Cruze) and goat ABC (Vector stain) and development of
DAB, it is found that the intensity of the band of 46 Kd is very week.
Instead, the intensity of 23 Kd is very strong in reducing condition.
Why is that? My sample is rat retina.
Thank you for your opinion!
Platini
