15 October 2018 2 3K Report

I am running a western blot assay using whole tissue homogenates. The homogenates are from collected mouse brains and I am using two groups an Ames dwarf mouse and a wild-type mouse.

I see that in the literature several groups are using B-actin and not GAPDH.

Why would one choose GAPDH vs B-actin? Does someone have a resource with rationale for either loading control?

More Cody Boyle's questions See All
Similar questions and discussions