c-Src(Phospho Tyr419) Polyclonal Antibody, 20ul[BT-AP06923] Cell Screening and Imaging Defects in TMEM237 are a

Defects in TMEM237 are a cause of Joubert syndrome-14

Special central suspension design protects monolayer cells while preventing cell culture medium loss

This protein regulates Myotonic Dystrophy Protein Kinase

Shorter isoforms of this protein which lack the C-terminal HECT domain are therefore unlikely to bind E2 enzymes

c-Src(Phospho Tyr419) Polyclonal Antibody, 20ul[BT-AP06923] Cell Screening and Imaging Defects in TMEM237 are aThis gene is highly similar to the v src gene of Rous sarcoma virus. This proto oncogene may play a role in the regulation of embryonic development and cell growth. The protein encoded by this gene is a tyrosine protein kinase whose activity can be inhibited by phosphorylation by c SRC kinase. Mutations in this gene could be involved in the malignant progression of colon cancer. Two transcript variants encoding the same protein have been found for