NFKappaB-p65 Polyclonal Antibody, 20ul[BT-AP05992] Gene Synthesis Mutations in SLC24A1 may play

Mutations in SLC24A1 may play a role in congenital stationary night blindness

which promotes cholesterol efflux from tissues to the liver for excretion

Mutations in this gene lead to an accumulation of GM2 ganglioside in neurons

An important paralog of this gene is GPR61

CMTM8 acts as a tumor suppressor

NFKappaB-p65 Polyclonal Antibody, 20ul[BT-AP05992] Gene Synthesis Mutations in SLC24A1 may playNF kappa B is a ubiquitous transcription factor involved in several biological processes. It is held in the cytoplasm in an inactive state by specific inhibitors. Upon degradation of the inhibitor, NF kappa B moves to the nucleus and activates transcription of specific genes. NF kappa B is composed of NFKB1 or NFKB2 bound to either REL, RELA, or RELB. The most abundant form of NF kappa B is NFKB1 complexed with the product of RELA, RELA. Four