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S6A19 rabbit pAb

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],

Product Specifications

Background

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]

UniProt

Q695T7

Swiss Prot

Q695T7

Reactivity

Human; Rat; Mouse

Immunogen

Synthesized peptide derived from part region of human protein

Clonality

Polyclonal

Source

Rabbit

Applications

WB; ELISA

Concentration

1 mg/ml

Dilution

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

Molecular Weight

69kD

Storage Conditions

-20°C/1 year

Observed Molecular Weight

69kD

Fragment

IgG

Subcellular Location

Cell membrane ; Multi-pass membrane protein . Apical cell membrane ; Multi-pass membrane protein . Colocalizes with ACE2 on the apical membrane of cells lining villi of the jejunum, ileum and on kidney proximal tubules. .

Gene ID (Human)

340024

Available Sizes

Curated Selection

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