The 9 kDa calcium-binding protein, calbindin9kDa, was discovered to be soluble in 7% (v/v) perchloric acid. Calbindin9kDa was simply purified from rat duodenum in 1
Two micromethods for measuring proteolytic activity were developed. A semiquantitative assay on microtitre plates with granular Azocoll as substrate is based on the determination of
Native protein separations by capillary gel electrophoresis are achieved utilizing linear acrylamide gel matrices. Polyacrylamide gels with a focus vary of three.5-5% didn’t exhibit measurement
