SLC7A9 polyclonal antibody
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More Files
- More Functions
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human kidney with SLC7A9 polyclonal antibody (Cat # PAB27931) shows strong membranous positivity in renal tubules at 1:1000-1:2500 dilution.
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Specification
Product Description
Rabbit polyclonal antibody raised against recombinant SLC7A9.
Immunogen
Recombinant protein corresponding to amino acids of human SLC7A9.
Sequence
YKFGWAQKISKPITMHLQMLMEVVPPEEDPE
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunohistochemistry (1:1000-1:2500)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human kidney with SLC7A9 polyclonal antibody (Cat # PAB27931) shows strong membranous positivity in renal tubules at 1:1000-1:2500 dilution. -
Gene Info — SLC7A9
Entrez GeneID
11136Gene Name
SLC7A9
Gene Alias
BAT1, CSNU3, FLJ94301
Gene Description
solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
Gene Ontology
HyperlinkGene Summary
This gene encodes a protein that belongs to a family of light subunits of amino acid transporters. This protein plays a role in the high-affinity and sodium-independent transport of cystine and neutral and dibasic amino acids, and appears to function in the reabsorption of cystine in the kidney tubule. Mutations in this gene cause non-type I cystinuria, a disease that leads to cystine stones in the urinary system due to impaired transport of cystine and dibasic amino acids. Two transcript variants, which encode the same protein, have been found for this gene. [provided by RefSeq
Other Designations
B(0,+)-type amino acid transporter 1|bo,+ amino acid transporter|glycoprotein-associated amino acid transporter b0,+AT1|solute carrier family 7, member 9
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Disease
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