anti-Solute Carrier Family 52 (Riboflavin Transporter), Member 2 (SLC52A2) Antibodies

SLC52A2 encodes a membrane protein which belongs to the riboflavin transporter family.

list all antibodies Gene Name GeneID UniProt
Anti-Human SLC52A2 SLC52A2 79581 Q9HAB3
Anti-Rat SLC52A2 SLC52A2 362942 B5MEV3
Anti-Mouse SLC52A2 SLC52A2 52710 Q9D8F3
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Top anti-Solute Carrier Family 52 (Riboflavin Transporter), Member 2 Antibodies at antibodies-online.com

Showing 7 out of 8 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Rabbit Un-conjugated WB Western blot analysis of GPR172A expression in human brain (A) whole cell lysates. 200 μL Log in to see 13 to 14 Days
$487.50
Details
Human Rabbit Un-conjugated ELISA, IF, WB 100 μL Log in to see 16 Days
$181.73
Details
Human Rabbit Biotin WB   100 μL Log in to see 14 to 21 Days
$383.90
Details
Human Rabbit HRP WB   100 μL Log in to see 14 to 21 Days
$405.90
Details
Human Rabbit Un-conjugated WB   100 μL Log in to see 11 to 16 Days
$312.70
Details
Human Rabbit Un-conjugated IHC Immunohistochemistry: GPR172A Antibody [NBP2-49382] - Staining of human small intestine shows moderate cytoplasmic and membranous positivity in glandular cells. 0.1 mL Log in to see 10 to 13 Days
$491.63
Details
Human Rabbit Un-conjugated WB Lane 1: Cerebrum lysates Lane 2: Cerebrum lysates probed with GPR172A Polyclonal Antibody, Unconjugated  at 1:300 dilution and 4˚C overnight incubation. Followed by conjugated secondary antibody incubation at 1:10000 for 60 min at 37˚C. 100 μL Log in to see 3 to 7 Days
$306.90
Details

More Antibodies against Solute Carrier Family 52 (Riboflavin Transporter), Member 2 Interaction Partners

Human Solute Carrier Family 52 (Riboflavin Transporter), Member 2 (SLC52A2) interaction partners

  1. RFVT2 (show GPR172A Antibodies) gene and protein expression levels were higher in DLD (show DLD Antibodies)-1 and HT-29 compared to Caco2 cells. In tumor tissues of patients with CRC (show CALR Antibodies), RFVT2 (show GPR172A Antibodies) gene expression levels were increased, while protein expression was reduced, with a small reduction in riboflavin amount.

  2. This is the second report of the genotype-phenotype correlation between this syndrome named spinocerebellar ataxia with blindness and deafness type 2 (SCABD2) and SLC52A2 (show GPR172A Antibodies) gene.

  3. Eight mutations in SLC52a2 were associated with Brown-Vialetto-Van Laere syndrome.

  4. A novel SLC52A2 mutation identified in a family with spinocerebellar ataxia with blindness and deafness.

  5. This study showed that Auditory neuropathy in Brown-Vialetto-Van (show TNIP1 Antibodies) Laere syndrome due to riboflavin transporter RFVT2 (show GPR172A Antibodies) deficiency and improved by riboflavin treatment.

  6. These results strongly implicate a potential role for SLC52A2 in riboflavin uptake by milk-producing MECs, a critical step in the transfer of riboflavin into breast milk.

  7. Mutations in SLC52A2 result in a recognizable phenotype distinct from Brown-Vialetto-Van-Laere syndrome.

  8. data suggest that MMND is a distinct clinical subgroup of childhood onset MND (show CLN8 Antibodies) patients where the known genetic defects are so far negative.

  9. We demonstrate that SLC52A2 (show GPR172A Antibodies) mutations cause reduced riboflavin uptake and reduced riboflavin transporter protein (show HNRNPU Antibodies) expression

  10. summary of recent findings on the cloning, nomenclature, functional characterization and genetic diseases of RFVT1/SLC52A1, RFVT2/SLC52A2 and RFVT3/SLC52A3 [review]

Mouse (Murine) Solute Carrier Family 52 (Riboflavin Transporter), Member 2 (SLC52A2) interaction partners

Solute Carrier Family 52 (Riboflavin Transporter), Member 2 (SLC52A2) Antigen Profile

Protein 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.

Gene names and symbols associated with SLC52A2

  • solute carrier family 52 member 2 (SLC52A2) antibody
  • solute carrier family 52 member 2 (Slc52a2) antibody
  • solute carrier protein 52, member 2 (Slc52a2) antibody
  • solute carrier family 52 (riboflavin transporter), member 2 (slc52a2) antibody
  • 2010003P03Rik antibody
  • BVVLS2 antibody
  • D15Ertd747e antibody
  • fc11c06 antibody
  • GPCR41 antibody
  • GPCR42 antibody
  • Gpr172a antibody
  • Gpr172b antibody
  • hRFT3 antibody
  • mRFT1 antibody
  • PAR1 antibody
  • PAR2 antibody
  • RFT3 antibody
  • RFVT2 antibody
  • RGD1560410 antibody
  • rRFT1 antibody
  • wu:fc11c06 antibody
  • zgc:63774 antibody

Protein level used designations for SLC52A2

G protein-coupled receptor 172A , PERV-A receptor 1 , porcine endogenous retrovirus A receptor 1 , putative G-protein coupled receptor GPCR41 , riboflavin transporter 3 , solute carrier family 52, riboflavin transporter, member 2 , G protein-coupled receptor 172B , porcine endogenous retrovirus A receptor 2 , riboflavin transporter 1 , PERV-A receptor 2 homolog , porcine endogenous retrovirus A receptor 2 homolog , gpr172a

GENE ID SPECIES
79581 Homo sapiens
362942 Rattus norvegicus
52710 Mus musculus
323832 Danio rerio
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