AP1M2 Rabbit Polyclonal Antibody, 50ul Metabolic enzymes Defects in VCL are the

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

This protein is a secreted enzyme that is proposed to regulate the availability of insulin-like growth factors (IGFs) by cleaving IGF-binding proteins

This gene is a member of the phospholipase D family and contains two PLD phosphodiesterase domains

There is a pseudogene for ARMCX2 on chromosome 7

It is a member of the Ig-superfamily containing 2 Ig-like domains of the V-set

AP1M2 Rabbit Polyclonal Antibody, 50ul Metabolic enzymes Defects in VCL are theThis gene encodes a subunit of the heterotetrameric adaptor related protein comlex 1 (AP 1), which belongs to the adaptor complexes medium subunits family. This protein is capable of interacting with tyrosine based sorting signals. Alternative splicing results in multiple transcript variants.