DRA rabbit pAb

DRA rabbit pAb

AO-06-ES4147-100

DRA rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES4147
Product nameDRA rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameSLC26A3; DRA; Chloride anion exchanger; Down-regulated in adenoma; Protein DRA; Solute carrier family 26 member 3
Size100μL
Unit price ($)248
Human gene ID1811
Human Swiss-ProtP40879
SourceRabbit
IsotypeIgG
TargetDRA
Fields>>Pancreatic secretion;>>Mineral absorption
Gene nameSLC26A3
Protein nameChloride anion exchanger
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID13487
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9WVC8
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID114629
Rat gene linkView Rat Gene
Rat Swiss-ProtQ924C9
Rat Swiss linkView Rat Swiss-Prot
ImmunogenSynthesized peptide derived from the C-terminal region of human DRA.
SpecificityDRA Polyclonal Antibody detects endogenous levels of DRA protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)84kD
BackgroundThe protein encoded by this gene is a transmembrane glycoprotein that transports chloride ions across the cell membrane in exchange for bicarbonate ions. It is localized to the mucosa of the lower intestinal tract, particularly to the apical membrane of columnar epithelium and some goblet cells. The protein is essential for intestinal chloride absorption, and mutations in this gene have been associated with congenital chloride diarrhea. [provided by RefSeq, Oct 2008],
Functiondevelopmental stage:Expression is significantly decreased in adenomas (polyps) and adenocarcinomas of the colon.,disease:Defects in SLC26A3 are the cause of congenital chloride diarrhea (CLD) [MIM:214700]. CLD is a disease characterized by voluminous watery stools containing an excess of chloride. The children with this disease are often premature.,function:Chloride/bicarbonate exchanger. Involved in absorbtion of in the colon. Helps mediate electrolyte and fluid absorption.,PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Belongs to the SLC26A/SulP transporter (TC 2.A.53) family.,similarity:Contains 1 STAS domain.,subunit:Interacts with PDZK1.,
Subcellular locationApical cell membrane ; Multi-pass membrane protein . Membrane ; Multi-pass membrane protein . Localized in sperm membranes. Midpiece of sperm tail. Colocalizes with CFTR at the midpiece of sperm tail (By similarity). .
ExpressionColon,Lung,Rectum tumor,

Additional Images

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Western Blot analysis of 293, HeLa cells using DRA Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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: AO-06-ES4147-100
: 10 Items
Hurry! only 10 items left in stock.

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