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

Matrix metallopeptidase 3 is thought to be involved in wound repair

APOC3 and APOA4 genes are closely linked in both rat and human genomes

This protein regulates Myotonic Dystrophy Protein Kinase

Three related pseudogenes are located within the Smith-Magenis syndrome region on chromosome 17

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