KLOT Polyclonal Antibody, 20ul Metabolic enzymes Mutations in this gene are

Mutations in this gene are associated with the autosomal recessive disorder congenital disorder of glycosylation| type IIk

KDa Mitochondrial Proteolipid

This gene encodes a receptor that belongs to the protein tyrosine kinase Tie2 family

It is active on peptide linkages involving the carboxyl group of lysine or arginine

NOL3 encodes an anti-apoptotic protein nucleolar protein 3 that has been shown to down-regulate the enzyme activities of caspase 2

KLOT Polyclonal Antibody, 20ul Metabolic enzymes Mutations in this gene areThis gene encodes a type I membrane protein that is related to beta glucosidases. Reduced production of this protein has been observed in patients with chronic renal failure (CRF), and this may be one of the factors underlying the degenerative processes (e. g., arteriosclerosis, osteoporosis, and skin atrophy) seen in CRF. Also, mutations within this protein have been associated with ageing and bone loss.