SLC26A3 anticorps

N° du produit ABIN2457907

Détail du produit anti-SLC26A3 anticorps

Antigène: SLC26A3 (Solute Carrier Family 26, Member 3 (SLC26A3))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLC26A3 est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SLC26A3.

Information d'application

Indications d'application: SLC26A3 antibody can be used for detection of SLC26A3 by ELISA at 1:312500. SLC26A3 antibody can be used for detection of SLC26A3 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store SLC26A3 antibody at -20 °C.

Détails sur SLC26A3

Antigène: SLC26A3 (Solute Carrier Family 26, Member 3 (SLC26A3))

Autre désignation: SLC26A3 (SLC26A3 Produits)

Synonymes: anticorps CLD, anticorps DRA, anticorps 9030623B18Rik, anticorps 9130013M11Rik, anticorps AV376035, anticorps Dra, anticorps si:dkey-31f5.2, anticorps SLC26A3, anticorps solute carrier family 26 member 3, anticorps solute carrier family 26, member 3, anticorps solute carrier family 26 (anion exchanger), member 3, anticorps SLC26A3, anticorps Slc26a3, anticorps slc26a3.1

Sujet: SLC26A3 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.The protein encoded by this gene is a transmembrane glycoprotein that functions as a sulfate transporter. It is localized to the mucosa of the lower intestinal tract, particularly to the apical membrane of columnar epithelium and some goblet cells. Mutations in this gene have been associated with congenital chloride diarrhea. Please see the Entrez Gene record to access additional publications.

Poids moléculaire: 84 kDa

ID gène: 1811

NCBI Accession: NP_000102

UniProt: P40879