STAC2 Polyclonal Antibody, 50ul Antibody Development Mutations in this gene cause

Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen)

The Sentrin-specific protease 8 is involved in processing and deconjugation of the ubiquitin-like protein termed

The ligand of this receptor is macrophage inflammatory protein 3 alpha(MIP-3 alpha)

the encoded protein forms homo- or hetero-dimers that interact with specific DNA sequences to activate transcription

STAC2 Polyclonal Antibody, 50ul Antibody Development Mutations in this gene causeIn skeletal muscles contraction, may play a role in neuromuscular synaptic transmission.