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Recombinant Human SLC19A2 cell lysate

Cat.No. : SLC19A2-1617HCL
  • Specification
  • Gene Information
  • Related Products
Description : This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness.
Species : Human
Size : 100 ul
Storage Buffer : 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications : Western Blot;
Gene Name : SLC19A2 solute carrier family 19 (thiamine transporter), member 2 [ Homo sapiens ]
Official Symbol : SLC19A2
Synonyms : SLC19A2; solute carrier family 19 (thiamine transporter), member 2; TRMA; thiamine transporter 1; THTR1; thTr-1; solute carrier family 19 member 2; high affinity thiamine transporter; reduced folate carrier protein (RFC) like; TC1; THT1; THMD1;
Gene ID : 10560
mRNA Refseq : NM_006996
Protein Refseq : NP_008927
MIM : 603941
UniProt ID : O60779
Chromosome Location : 1q23.3
Pathway : Metabolism, organism-specific biosystem; Metabolism of vitamins and cofactors, organism-specific biosystem; Metabolism of water-soluble vitamins and cofactors, organism-specific biosystem; Vitamin B1 (thiamin) metabolism, organism-specific biosystem; Vitamin digestion and absorption, organism-specific biosystem; Vitamin digestion and absorption, conserved biosystem;
Function : folic acid binding; folic acid transporter activity; reduced folate carrier activity; thiamine transmembrane transporter activity; thiamine uptake transmembrane transporter activity;

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For Research Use Only. Not intended for any clinical use. No products from Creative BioMart may be resold, modified for resale or used to manufacture commercial products without prior written approval from Creative BioMart.

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