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Solute Carrier Family 19, Member 3 (Slc19a3) ELISA Kits

Slc19a3 encodes a ubiquitously expressed transmembrane thiamine transporter that lacks folate transport activity. Additionally we are shipping Solute Carrier Family 19, Member 3 Antibodies (30) and Solute Carrier Family 19, Member 3 Proteins (4) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human Slc19a3 Slc19a3 80704 Q9BZV2
Anti-Rat Slc19a3 Slc19a3 316559  
Anti-Mouse Slc19a3 Slc19a3 80721 Q99PL8
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More ELISA Kits for Solute Carrier Family 19, Member 3 Interaction Partners

Human Solute Carrier Family 19, Member 3 (Slc19a3) interaction partners

  1. Species differences in the substrate specificity of THTR-2 between human and mouse orthologues were observed.

  2. large genomic deletions occur in the regulatory region of SLC19A3 in Biotin-Thiamine-Responsive Basal Ganglia Encephalopathy

  3. Genetic variation in the SLC19A3 thiamine transporter at 2:228563818T/C may make a modest contribution towards the genetic susceptibility to alcohol dependence syndrome.

  4. This study provided evidence that biotin-thiamine-responsive basal ganglia disease is the result of SLC19A2 (show SLC19A2 ELISA Kits) mutation.

  5. TM4SF4 (show TM4SF4 ELISA Kits) interacts with hTHTR-2 and influences the physiological function of the thiamine transporter in human intestinal epithelial cells.

  6. These studies demonstrate that the human intestinal thiamine uptake is adaptively regulated by the extracellular substrate level via transcriptional regulation of the THTR-2 system, and that SP1 (show PSG1 ELISA Kits) transcriptional factor is involved in this regulation.

  7. A new, severe phenotype of SLC19A3 is identified in early-infantile, lethal encephalopathy characterized by subtotal brain degeneration.

  8. Our data shows that SLC19A3 is a new candidate for mutation screening in patients with Leigh syndrome

  9. Two Spanish siblings with a biotin-responsive basal ganglia disease phenotype and mutations in SLC19A3 presented with acute episodes of generalized dystonia

  10. These results suggested that aberrant SLC19A3 promoter hypermethylation in plasma may be a novel biomarker for breast and gastric cancer diagnosis.

Mouse (Murine) Solute Carrier Family 19, Member 3 (Slc19a3) interaction partners

  1. THTR-2 is required for normal uptake of thiamin in the intestine and can fulfill normal levels of uptake in conditions associated with THTR-1 (show DDA1 ELISA Kits) dysfunction.

  2. Pancreatic beta cells and islets take up thiamine by a regulated THTR1 (show DDA1 ELISA Kits)/2-mediated process.

Solute Carrier Family 19, Member 3 (Slc19a3) Antigen Profile

Antigen Summary

This gene encodes a ubiquitously expressed transmembrane thiamine transporter that lacks folate transport activity. Mutations in this gene cause biotin-responsive basal ganglia disease (BBGD)\; a recessive disorder manifested in childhood that progresses to chronic encephalopathy, dystonia, quadriparesis, and death if untreated. Patients with BBGD have bilateral necrosis in the head of the caudate nucleus and in the putamen. Administration of high doses of biotin in the early progression of the disorder eliminates pathological symptoms while delayed treatment results in residual paraparesis, mild mental retardation, or dystonia. Administration of thiamine is ineffective in the treatment of this disorder. Experiments have failed to show that this protein can transport biotin. Mutations in this gene also cause a Wernicke's-like encephalopathy.

Gene names and symbols associated with Slc19a3

  • solute carrier family 19, member 3 (slc19a3) antibody
  • solute carrier family 19, member 3 (SLC19A3) antibody
  • solute carrier family 19, member 3b (slc19a3b) antibody
  • solute carrier family 19, member 3 (LOC100230080) antibody
  • solute carrier family 19 (thiamine transporter), member 3 (SLC19A3) antibody
  • solute carrier family 19 (thiamine transporter), member 3 (Slc19a3) antibody
  • solute carrier family 19, member 3 (Slc19a3) antibody
  • A230084E24Rik antibody
  • AI788884 antibody
  • BBGD antibody
  • MGC52872 antibody
  • MGC89434 antibody
  • si:dkey-223n17.4 antibody
  • slc19a3 antibody
  • THMD2 antibody
  • ThTr2 antibody

Protein level used designations for Slc19a3

solute carrier family 19, member 3 , thiamine transporter 2 , thiamine transporter 2-like , thTr-2 , solute carrier family 19 (sodium/hydrogen exchanger), member 3

GENE ID SPECIES
379156 Xenopus laevis
424792 Gallus gallus
448431 Xenopus (Silurana) tropicalis
470667 Pan troglodytes
549052 Xenopus (Silurana) tropicalis
556920 Danio rerio
709554 Macaca mulatta
100230080 Taeniopygia guttata
100341170 Oryctolagus cuniculus
100445161 Pongo abelii
80704 Homo sapiens
316559 Rattus norvegicus
486151 Canis lupus familiaris
537280 Bos taurus
80721 Mus musculus
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