ERMAP Polyclonal Antibody, 100ul Pipette Controller Defects in HSPB1 are a

Defects in HSPB1 are a cause of Charcot-Marie-Tooth disease type 2F (CMT2F) and distal hereditary motor neuropathy (dHMN)

One such pathway is the p53-HDM2-p21(WAF1) pathway

and a second gene that encodes both the RhC and RhE antigens on a single polypeptide

Conquer any challenge with the EasyGo

a variable cytoplasmic loop

ERMAP Polyclonal Antibody, 100ul Pipette Controller Defects in HSPB1 are aThe protein encoded by this gene is a cell surface transmembrane protein that may act as an erythroid cell receptor, possibly as a mediator of cell adhesion. Polymorphisms in this gene are responsible for the Scianna Radin blood group system. Two transcript variants encoding the same protein have been found for this gene.