RGMA Polyclonal Antibody, 100ul Vortex Mixer Mutations in this gene cause

Mutations in this gene cause coenzyme Q10 deficiency| a mitochondrial encephalomyopathy| and also COQ2 nephropathy| an inherited form of mitochondriopathy with primary renal involvement

The ubiquitous enzymes consist of heterodimers with distinct large| catalytic subunits associated with a common small| regulatory subunit

also known as putative tumor suppressor protein 101F6

GTPase-activating proteins

The protein encoded by this gene is PPAR-gamma and is a regulator of adipocyte differentiation

RGMA Polyclonal Antibody, 100ul Vortex Mixer Mutations in this gene causeThis gene encodes a member of the repulsive guidance molecule family. The encoded protein is a glycosylphosphatidylinositol anchored glycoprotein that functions as an axon guidance protein in the developing and adult central nervous system. This protein may also function as a tumor suppressor in some cancers. Alternate splicing results in multiple transcript variants.