S6A19 Polyclonal Antibody

• Background :

  Solute carrier family 6 member 19 (SLC6A19) Homo sapiens 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. [provided by RefSeq, Jul 2008]

• Gene ID :

  340024

• Swiss Prot :

  Q695T7

• Cross Reactivity :

  Human; Rat; Mouse

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB; ELISA

• Dilution :

  WB 1:500-2000 ELISA 1:5000-20000

• Buffer :

  Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.

• Molecular Weight :

  69

• Storage Conditions :

  -20°C/1 year

• Protein Weight :

  69