COQ2 Rabbit Polyclonal Antibody, 20ul Custom RNA Oligos With a potency of 1000

With a potency of 1000 U and a concentration of 10 U/μl

With 96 tests included

Mutations in NRXN1 are associated with Pitt-Hopkins-like syndrome-2 and may contribute to susceptibility to schizophrenia

such as adenylate cyclase

The delta subunit mediates the dependence of the enzyme on calcium concentration

COQ2 Rabbit Polyclonal Antibody, 20ul Custom RNA Oligos With a potency of 1000This gene encodes an enzyme that functions in the final steps in the biosynthesis of CoQ (ubiquinone) a redox carrier in the mitochondrial respiratory chain and a lipid soluble antioxidant. This enzyme which is part of the coenzyme Q10 pathway catalyzes the prenylation of parahydroxybenzoate with an all trans polyprenyl group. Mutations in this gene cause coenzyme Q10 deficiency a mitochondrial encephalomyopathy and also COQ2 nephropathy an inherited