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SL9A3 Polyclonal Antibody

SL9A3 Polyclonal Antibody

Views(4) Publications(0) Catalog no(ABP60420)
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Specification

Product name SL9A3 Polyclonal Antibody
Immunogen Synthesized peptide derived from part region of human SL9A3 protein at amino acid sequence of 490-570
Host Rabbit
Reactivity Human,Rat
Applications WB,ELISA
Applications notes Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-2000;ELISA 1:5000-20000
Clonality Polyclonal
Preparation method The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Alternative Sodium/hydrogen exchanger 3; Na(+)/H(+) exchanger 3; NHE-3; Solute carrier family 9 member 3

Product Properties

Formulation Liquid solution
Concentration 1 mg/ml
Molecular weight 91kD
Storage buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Storage instructions Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
Shipping Gel pack with blue ice.
Precautions The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Additional Information

Background SLC9A3 (Solute Carrier Family 9 Member A3) is a Protein Coding gene. Diseases associated with SLC9A3 include Diarrhea 8, Secretory Sodium, Congenital and Diarrhea 3, Secretory Sodium, Congenital, Syndromic. Among its related pathways are Collagen chain trimerization and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds. he protein encoded by this gene is an epithelial brush border Na/H exchanger that uses an inward sodium ion gradient to expel acids from the cell. Defects in SLC9A3 are a cause of congenital secretory sodium diarrhea. Pseudogenes of this gene exist on chromosomes 10 and 22.
Gene ID 6550
Alternative Sodium/hydrogen exchanger 3; Na(+)/H(+) exchanger 3; NHE-3; Solute carrier family 9 member 3
Others The antibody detects endogenous levels of SL9A3 protein
Accession P48764
Observed Band(KD) 91

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