RPGR1 Rabbit Polyclonal Antibody, 20ul General Lab Use Mutations in CYP7B1 have been

Mutations in CYP7B1 have been associated with hereditary spastic paraplegia (SPG5 or HSP)

neuronal differentiation and migration

The parts in contact with liquids are autoclavable

This gene encodes a nuclear protein with three C2H2-type zinc fingers| and functions as a transcriptional repressor

Mutations of this gene cause carboxylesterase 1 deficiency

RPGR1 Rabbit Polyclonal Antibody, 20ul General Lab Use Mutations in CYP7B1 have beenThis gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness.