OSTCN Polyclonal Antibody, 100ul Immune Cell Analysis and phospholipid hydroperoxides

and phospholipid hydroperoxides

but the full-length nature and biological activity of only two variants are determined

This gene contains stretches of trinucleotide repeats and is located in the chromosome 22 region which is deleted in DiGeorge syndrome

including interleukins 2

The beta subunit may assist in binding of the phospholipid substrate (Probable)

OSTCN Polyclonal Antibody, 100ul Immune Cell Analysis and phospholipid hydroperoxidesThis gene encodes a highly abundant bone protein secreted by osteoblasts that regulates bone remodeling and energy metabolism. The encoded protein contains a Gla (gamma carboxyglutamate) domain, which functions in binding to calcium and hydroxyapatite, the mineral component of bone. Serum osteocalcin levels may be negatively correlated with metabolic syndrome. Read through transcription exists between this gene and the neighboring upstream gene, PMF1