MYOF Rabbit Polyclonal Antibody, 20ul DNA Synthesis Mutations in this gene cause

Mutations in this gene cause nemaline myopathy type 3

and also catalyzes the formation of riboflavin 4'

DOR-1 is a receptor for enkephalins

Alternate splicing results in multiple transcript variants that encode different isoforms

Human Mindin shares 88% amino acid sequence homology with mouse and rat proteins

MYOF Rabbit Polyclonal Antibody, 20ul DNA 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