SKU: WP15459 Categories: ,

DRA Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP15459-100
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Product details

Background:

The 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],

Specifications

Size50μL/100μL
TargetDRA
ReactivityHuman, Mouse, Rat
ApplicationsWB, ELISA
MW(Calculated)
MW(Observed)84kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; ELISA 1:20000; Not yet tested in other applications.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from the C-terminal region of human DRA.
SpecificityDRA Polyclonal Antibody detects endogenous levels of DRA protein.
Gene NameSLC26A3
Protein NameChloride anion exchanger
Other NameSLC26A3; / DRA; / Chloride anion exchanger; / Down-regulated in adenoma; / Protein DRA; / Solute carrier family 26 member 3
SpeciesHuman
Gene ID1811
UniprotP40879,
Species.1Mouse
Gene ID.113487
Uniprot.1Q9WVC8,
Species.2Rat
Gene ID.2114629
Uniprot.2Q924C9
Cellular LocalizationApical 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). .
Tissue ExpressionColon,Lung,Rectum tumor,
Signaling_pathway
Research Areas>>Pancreatic secretion; / >>Mineral absorption
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.,
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