STC1 Polyclonal Antibody, 50ul Immune Repertoire Sequencing The encoded protein may function

The encoded protein may function as a palmitoyltransferase

The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme

Catalytic activity:Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1)

This gene encodes a protein that plays a major role in the bidirectional stimulation of T and B cells

STC1 Polyclonal Antibody, 50ul Immune Repertoire Sequencing The encoded protein may functionThis gene encodes a secreted, homodimeric glycoprotein that is expressed in a wide variety of tissues and may have autocrine or paracrine functions. The gene contains a 5' UTR rich in CAG trinucleotide repeats. The encoded protein contains 11 conserved cysteine residues and is phosphorylated by protein kinase C exclusively on its serine residues. The protein may play a role in the regulation of renal and intestinal calcium and phosphate transport,