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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