Background:

This gene is predicted to encode a glycosylated| cationic amino acid transporter protein with 14 transmembrane domains. This gene is primarily expressed in skin fibroblasts| neural tissue| and primary endothelial cells and its protein is predicted to mediate lysosomal uptake of cationic amino acids. Mutations in this gene are associated with autosomal recessive retinitis pigmentosa. In mice| this gene is expressed in the photoreceptor layer of the retina where its expression increases over the course of retinal development and persists in the mature retina.

Classification:

Primary antibody

Alternative names:

S7A14; Probable cationic amino acid transporter; Solute carrier family 7 member 14

Species reactivity:

Human, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human S7A14

Concentration:

1 mg/ml

Molecular weight:

Applications:

WB

Storage:

-20°C for 1 year

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