GPR172B Polyclonal Antibody, 50ul Cytokines It is a type I

It is a type I membrane protein

Mutations in this gene are associated with autosomal SCID (severe combined immunodeficiency disease)

Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease

Y-linked) is located on the non-recombining region of the Y chromosome

subcellular location:Located on plasma membrane of neuroblastoma NMB7 cells

GPR172B Polyclonal Antibody, 50ul Cytokines It is a type IBiological redox reactions require electron donors and acceptor. Vitamin B2 is the source for the flavin in flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) which are common redox reagents. SLC52A1 (solute carrier family 52 member 1) encodes a member of the riboflavin (vitamin B2) transporter family. Haploinsufficiency of this protein can cause maternal riboflavin deficiency. Multiple alternatively spliced variants, encoding the same