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SLC7A9 Polyclonal Antibody, AbBy Fluor™ 594 Conjugated

Product Specifications

Background

SLC7A9 belongs to the amino acid-polyamine-organocation (APC) superfamily. It is a disulfide linked heterodimer with the amino acid transport protein SLC3A1. SLC7A9 is involved in the high affinity, sodium independent transport of cystine and neutral and dibasic amino acids (system b (0, +) -like activity) . Thought to be responsible for the high affinity reabsorption of cystine in the kidney tubule. Defects in SLC7A9 are a cause of non type I cystinuria (CSNU) . CSNU arises from impaired transport of cystine and dibasic amino acids through the epithelial cells of the renal tubule and gastrointestinal tract. Three types of cystinuria have been described: type I (fully recessive or silent) ; type II (high excretor) ; type III (moderate excretor) . Defects in SLC7A9 are associated with type II and type III cystinuria. They also might account for some non classic type I cystinuria cases.

Synonyms

B (0+) type amino acid transporter 1; BAT1; CSNU3; Glycoprotein associated amino acid transporter b0+AT1; Solute carrier family 7 (cationic amino acid transporter y+ system) member 9; BAT1_HUMAN; B (0, +) -type amino acid transporter 1; B (0, +) AT; Glycoprotein-associated amino acid transporter b0, +AT1; Solute carrier family 7 member 9.

Gene ID

11136

Swiss Prot

P82251

Cellular Locus

Cell membrane

Host

Rabbit

Cross Reactivity

Human

Target

SLC7A9

Clonality

Polyclonal

Isotype

IgG

Conjugation

AbBy Fluor™ 594

Source

Recombinant human SLC7A9 protein

Applications

WB

Purification

Purified by Protein A.

Excitation Emission

590nm/617nm

Concentration

1µg/µl

Dilution

WB (1:300-5000)

Buffer

Aqueous buffered solution containing 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.

Modification

Unmodified

Storage Conditions

Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Gene ID URL

11136

Predicted Cross Reactivity

Mouse, Rat

Curated Selection

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