"SLC19A2" Related Products

Recombinant Human SLC19A2 cell lysate

Cat.No.: SLC19A2-1617HCL
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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