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SLC7A9 Polyclonal Antibody, RBITC 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

RBITC

Source

Recombinant human SLC7A9 protein

Applications

WB

Purification

Purified by Protein A.

Excitation Emission

570nm/595nm

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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