SRPK2 Polyclonal Antibody, 100ul Liquid Handling ＆Storage Defects in this gene may

Defects in this gene may be a cause of autosomal recessive spinocerebellar ataxia-10

liver and pancreas

and it is the ligand for two proteins at the cell surface of T cells

a kidney disorder involving both tubules and glomeruli

SRPK2 Polyclonal Antibody, 100ul Liquid Handling ＆Storage Defects in this gene mayCatalytic activity: ATP + a protein = ADP + a phosphoprotein.,cofactor: Magnesium.,enzyme regulation: Activated by phosphorylation on Ser 52 and Ser 588.,Phosphorylates RS domain containing proteins, such as SFRS1 and SFRS2 on serine residues. Role in spliceosome assembly and in mediating the trafficking of splicing factors. Appears to mediate HBV core protein phosphorylation which is a prerequisite for pregenomic RNA encapsidation into viral