PBFE Polyclonal Antibody, 50ul PCR Series The encoded protein lacks detectable

The encoded protein lacks detectable catalytic tyrosine kinase activity

The encoded protein may be involved in O-linked glycosylation of the immunoglobulin A1 hinge region

In mice| it has been shown to be essential for correct myelination in the peripheral nervous system

Interacts with SV40 major capsid protein VP1

Mutations in this gene cause the syndrome of apparent mine

PBFE Polyclonal Antibody, 50ul PCR Series The encoded protein lacks detectableEnoyl CoA hydratase and 3 hydroxyacyl CoA dehydrogenase by EHHADH is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta oxidation pathway. The N terminal region of the encoded protein contains enoyl CoA hydratase activity while the C terminal region contains 3 hydroxyacyl CoA dehydrogenase activity. Defects in EHHADH are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different