TGM3 Polyclonal Antibody, 100ul Live Cell Imaging Defects in this gene are

Defects in this gene are a cause of chromosome 9q subtelomeric deletion syndrome (9q-syndrome

Activity of this protein is important in promoting the survival of dopaminergic neurons

The protein encoded by this gene belongs to a subfamily of tyrosine kinase receptors with homology to Dictyostelium discoideum protein discoidin I in their extracellular domain

The protein encoded by KLF7 (Kruppel like factor 7)is a member of the Kruppel-like transcriptional regulator family

TGM3 Polyclonal Antibody, 100ul Live Cell Imaging Defects in this gene areTransglutaminases are enzymes that catalyze the crosslinking of proteins by epsilon gamma glutamyl lysine isopeptide bonds. While the primary structure of transglutaminases is not conserved, they all have the same amino acid sequence at their active sites and their activity is calcium dependent. The protein encoded by this gene consists of two polypeptide chains activated from a single precursor protein by proteolysis. The encoded protein is involved