Background:

This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Alternate transcript variants, which encode the same protein, have been found for this gene.

Applications:

ELISA, IHC

Name of antibody:

SLC7A9

Immunogen:

Synthetic peptide of human SLC7A9

Full name:

solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9

Synonyms：

BAT1; CSNU3

SwissProt:

P82251

ELISA Recommended dilution:

2000-5000

IHC positive control:

Human liver cancer and Human thyroid cancer

IHC Recommend dilution:

25-100