MYOF Rabbit Polyclonal Antibody, 50ul Gene Synthesis Mutations in this gene cause

Mutations in this gene cause deafness

This gene encodes a peroxisomal membrane protein that belongs to the family of mitochondrial solute carriers

This protein is expressed in spermatozoa and localized to the acrosomal region of the sperm head as well as the length of the principal piece

The encoded protein functions as a homodimer and interacts directly with both CSTF1 and CSTF2 in the CSTF complex

MYOF Rabbit Polyclonal Antibody, 50ul Gene Synthesis Mutations in this gene causeMutations in dysferlin a protein associated with the plasma membrane can cause muscle weakness that affects both proximal and distal muscles. The protein encoded by this gene is a type II membrane protein that is structurally similar to dysferlin. It is a member of the ferlin family and associates with both plasma and nuclear membranes. The protein contains C2 domains that play a role in calcium mediated membrane fusion events suggesting that it may