IDH3G Polyclonal Antibody, 100ul Immunology Defects in ATG16L1 are a

Defects in ATG16L1 are a cause of susceptibility to inflammatory bowel disease type 10 (IBD10)

This gene is thought to encode a GDP-mannose pyrophosphorylase

biologically inert and non-degradable

Tube body designed with both graduation and writing area for easy identification

SLC30A9 (Solute Carrier Family 30 Member 9) is a Protein Coding gene

IDH3G Polyclonal Antibody, 100ul Immunology Defects in ATG16L1 are aIsocitrate dehydrogenases catalyze the oxidative decarboxylation of isocitrate to 2 oxoglutarate. These enzymes belong to two distinct subclasses one of which utilizes NAD(+) as the electron acceptor and the other NADP(+). Five isocitrate dehydrogenases have been reported: three NAD(+) dependent isocitrate dehydrogenases which localize to the mitochondrial matrix and two NADP(+) dependent isocitrate dehydrogenases one of which is mitochondrial and the