3Beta-HSD7 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube heart and brain

heart and brain

The lid is ergonomically designed with thick stripes for easy screwing

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

Sporadic and familial mutations in this gene result in paragangliomas and pheochromocytoma

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

3Beta-HSD7 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube heart and brainHSD3B7 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