TSC2(Phospho Ser1254) Rabbit Polyclonal Antibody, 20ul Low retention tips Mutations in this gene have

Mutations in this gene have been associated with nemaline myopathy (NM)| a rare congenital muscle disorder

PPARs mediate a variety of biological processes

An experiment with transient gene expression demonstrated that this receptor was incapable of binding to interleukin 1 alpha and interleukin 1 beta with high affinity

and rats with one easy step

SOS2 (SOS Ras/Rho guanine nucleotide exchange factor 2) encodes a regulatory protein that is involved in the positive regulation of ras proteins

TSC2(Phospho Ser1254) Rabbit Polyclonal Antibody, 20ul Low retention tips Mutations in this gene havealternative products: Additional isoforms seem to exist. Experimental confirmation may be lacking for some isoforms disease: Defects in TSC2 are a cause of lymphangioleiomyomatosis (LAM)