Hck(Phospho Tyr410) Polyclonal Antibody, 100ul In vitro Assessment Defects in VCL are the

Defects in VCL are the cause of cardiomyopathy dilated type 1W

GO annotations related to this gene include cysteine-type endopeptidase activity and thiol-dependent ubiquitinyl hydrolase activity

and the truncated form additionally interacts with CCR1 and CCR2

CHAT encodes an enzyme which catalyzes the biosynthesis of the neurotransmitter acetylcholine

Hck(Phospho Tyr410) Polyclonal Antibody, 100ul In vitro Assessment Defects in VCL are theThe protein encoded by this gene is a member of the Src family of tyrosine kinases. This protein is primarily hemopoietic, particularly in cells of the myeloid and B lymphoid lineages. It may help couple the Fc receptor to the activation of the respiratory burst. In addition, it may play a role in neutrophil migration and in the degranulation of neutrophils. Multiple isoforms with different subcellular distributions are produced due to both