I am doing a cellulase isolation and purification from Bacillus sp. I have done the plate assay, and have got about 12 positive results from it, one of it is Bacillus subtilis. I want succinate buffer to give the gel a wash after I have run a crude enzyme extract denatured with SDS in Tris-Hcl buffer. The running buffer I have used is Tris-glycine. I want to maintain range of 4.8-5.8 pH of the washing buffer. I also need to stain the gel with Congo Red after the washing step.