GTX87976
PEVR1 antibody
Eine Lieferung in diese Region ist nicht möglich.
- SKU:
- GTX87976
- Zusätzliche Namen:
- BVVLS2 , D15Ertd747e , GPCR41 , GPR172A , PAR1 , RFT3 , RFVT2 , SLC52A2 , hRFT3 , solute carrier family 52 member 2 , PEVR1 , solute carrier family 52 (riboflavin transporter), member 2
- Anwendung:
- WB, IF, ICC
- Physischer Zustand:
- Liquid
- Spezies-Reaktivität:
- Human
- Aufreinigung:
- Affinity Purified
- Lagerbedingungen:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Hersteller:
- Genetex
- Host:
- Rabbit
- Reaktivitäten:
- Human
- Buffer:
- PBS, 150mM NaCl, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- The antiserum was produced against synthesized peptide derived from human PEVR1 (43-92).
- Uniprot:
- Q9HAB3
- Synonyme:
- BVVLS2;D15Ertd747e;G protein-coupled receptor 172A;GPCR41;GPR172A;hRFT3;PAR1;PERV-A receptor 1;porcine endogenous retrovirus A receptor 1;Protein GPR172A;putative G-protein coupled receptor GPCR41;RFT3;RFVT2;riboflavin transporter 3;solute carrier family 52 (riboflavin transporter), member 2;solute carrier family 52, riboflavin transporter, member 2
- Weitere Details:
- This gene encodes a membrane protein which belongs to the riboflavin transporter family. In humans, riboflavin must be obtained by intestinal absorption because it cannot be synthesized by the body. The water-soluble vitamin riboflavin is processed to the coenzymes flavin mononucleotide (FMN) and flavin adenine dinucleotide (FAD) which then act as intermediaries in many cellular metabolic reactions. Paralogous members of the riboflavin transporter gene family are located on chromosomes 17 and 20. Unlike other members of this family, this gene has higher expression in brain tissue than small intestine. Alternative splicing of this gene results in multiple transcript variants encoding the same protein. Mutations in this gene have been associated with Brown-Vialetto-Van Laere syndrome 2 - an autosomal recessive progressive neurologic disorder characterized by deafness, bulbar dysfunction, and axial and limb hypotonia. [provided by RefSeq, Jul 2012]
- Versandbedingungen:
- Blue Ice