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Merck

SLC52A2

solute carrier family 52 (riboflavin transporter), member 2

Synonymes:
BVVLS2, D15Ertd747e, GPCR41, GPR172A, PAR1, RFT3, RFVT2, hRFT3
Espèce(s):
ID UniProtKB:
ID du gène:
  • Human(79581) Summary: 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]
  • Mouse(52710) solute carrier protein 52, member 2
  • Rat(362942) solute carrier family 52, riboflavin transporter, member 2
  • Zebrafish(323832) solute carrier family 52, riboflavin transporter, member 2
  • sheep(101117771) solute carrier family 52, riboflavin transporter, member 2
  • naked mole-rat(101721412) solute carrier family 52, riboflavin transporter, member 2
  • domestic guinea pig(100734411) solute carrier family 52, riboflavin transporter, member 2

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Antibodies

Référence du produit
Description
Espèces réactives
Application
Anti-SLC52A2 antibody produced in rabbit, Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution,
Espèces réactives
human
Application
immunohistochemistry

esiRNA

Référence du produit
Description
Espèce(s)
MISSION® esiRNA, targeting human SLC52A2,
Espèce(s)
human