3Beta-HSD7 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube Mutations in this gene are

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

HECT domain E3 ubiquitin ligases transfer ubiquitin from E2 ubiquitin-conjugating enzymes to protein substrates

|subunit:Binds MBD1

It is a major contributor to the lubricating and viscoelastic properties of whole saliva

The protein encoded by this gene is an acatalytic member of the alpha-carbonic anhydrase subgroup

3Beta-HSD7 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube Mutations in this gene areHSD3B7 encodes an enzyme (hydroxy delta 5 steroid dehydrogenase, 3 beta and steroid delta isomerase 7) which is involved in the initial stages of the synthesis of bile acids from cholesterol and a member of the short chain dehydrogenase reductase superfamily. The encoded protein is a membrane associated endoplasmic reticulum protein which is active against 7 alpha hydrosylated sterol substrates. Mutations in HSD3B7 are associated with a congenital