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FIGURE: 1 / 10
Reconstitute in 100 µL of sterile water. Centrifuge to remove any insoluble material.
The antigen is homologous in rat.
Specificity of this antibody: SLC6A19.
This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: b(0)AT1; neutral amino acid transporter; slc6a19 {ECO:0000312|RGD:1594328}; Sodium-dependent neutral amino acid transporter B(0)AT1; solute carrier family 6 (neurotransmitter transporter), member 19; Solute carrier family 6 member 19; solute carrier family 6, member 19; System B(0) neutral amino acid transporter AT1
Gene Aliases: 4632401C08Rik; B0at1; B<0>AT1; Slc6a19; Xt3
UniProt ID: (Rat) Q2A865, (Mouse) Q9D687
Entrez Gene ID: (Rat) 664630, (Mouse) 74338
Molecular Function: primary active transporter
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