IDHP Polyclonal Antibody, 100ul[BT-AP08600] Biochemical Reagents Defects in this gene are

Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis

SCML2 encodes a member of the Polycomb group proteins

HMW-uPA can be further processed into the catalytically active low molecular weight urokinase-type plasminogen activator (LMW-uPA)

The protein encoded by CDC16 (cell division cycle 16) functions as a protein ubiquitin ligase and is a component of the multiprotein APC complex

Our DNase/RNase-free

IDHP Polyclonal Antibody, 100ul[BT-AP08600] Biochemical Reagents Defects in this gene areIsocitrate 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