SHIP-2 Polyclonal Antibody, 100ul Protein Post-translational Modification Defects in this gene are

Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency

This gene encodes a subunit of NADH:ubiquinone oxidoreductase (complex I)

three epidermal growth factor (EGF)-like domains and three fibronectin type III repeats

congenital heart disease and other features

Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing to generate mature polypeptides

SHIP-2 Polyclonal Antibody, 100ul Protein Post-translational Modification Defects in this gene arePhosphatidylinositol 3,4,5 trisphosphate 5 phosphatase 2 encoded by INPPL1 is an SH2 containing 5' inositol phosphatase that is involved in the regulation of insulin function. The encoded protein also plays a role in the regulation of epidermal growth factor receptor turnover and actin remodelling. Additionally, this gene supports metastatic growth in breast cancer and is a valuable biomarker for breast cancer.