IDH3B Polyclonal Antibody, 50ul In vitro Assessment Mutations in this gene cause

Mutations in this gene cause autosomal recessive spastic paraplegia 7

and the production of antiphospholipid autoantibodies

an inherited peripheral neuropathy

This cytokine is required for the T-cell-independent induction of interferon (IFN)-gamma

PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism

IDH3B Polyclonal Antibody, 50ul In vitro Assessment Mutations in this gene causeIsocitrate 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