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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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: 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
基因别名: 4632401C08Rik; B0at1; B<0>AT1; Slc6a19; Xt3
UniProt ID: (Rat) Q2A865, (Mouse) Q9D687
Entrez Gene ID: (Rat) 664630, (Mouse) 74338