SHIP2(Phospho-Tyr1135) Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Mutations in this gene cause

Mutations in this gene cause primary bile acid malabsorption (PBAM)

Take on new challenges with our 1000 mL Sterile Vacuum Upper Cup

The core complex possesses DNA-dependent ATPase activity

NF-kappa-B moves to the nucleus and activates transcription of specific genes

SHIP2(Phospho-Tyr1135) Rabbit Polyclonal Antibody, 20ul Lentiviral Packaging Mutations in this gene causeThe protein encoded by this gene 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.