SVOPL Rabbit Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in KRT10 are associated

Mutations in KRT10 are associated with epidermolytic hyperkeratosis

which functions downstream of the Ras family of membrane associated GTPases to which it binds directly

a blood-borne glycoprotein comprised of three pairs of nonidentical polypeptide chains

031 amino acid peripheral membrane protein of the Golgi apparatus that exists as two alternatively spliced isoforms

Methylenetetrahydrofolate reductase encoded by MTHFR catalyzes the conversion of 5

SVOPL Rabbit Polyclonal Antibody, 20ul Site-directed Mutagenesis Mutations in KRT10 are associatedThe protein encoded by this gene is thought to be a member of solute carrier family 22 which includes transmembrane proteins that transport toxins and drugs from the body. This gene is a paralog of the SVOP gene that encodes synaptic vesicle 2 related protein.