Anti-IRE1 Antibody

• Catalog Number: orb1474640
• Category: Antibodies
• Description: Rabbit polyclonal antibody to IRE1
• Target: ERN1
• Clonality: Polyclonal
• Species/Host: Rabbit
• Conjugation: Unconjugated
• Reactivity: Human, Mouse, Rat
• Form/Appearance: Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
• Buffer/Preservatives: Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
• Purification: The antibody was purified by immunogen affinity chromatography.
• Immunogen: Recombinant protein corresponding to human IRE1. The exact sequence is proprietary.
• UniProt ID: Q9EQY0, O75460
• Tested applications: IF, IH, WB
• Dilution range: WB (1/500 - 1/1000), IH (1/50 - 1/100), FC (1/50 - 1/100)
• Antibody Type: Primary Antibody
• Source: Rabbit
• Storage: Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
• Alternative names: IRE1; Serine/threonine-protein kinase/endoribonucl
• Note: For research use only
• Entrez: 78943, 2081

Western blot analysis of IRE1 expression in HEK293T (A), mouse liver (B), rat liver (C) whole cell lysates. (Predicted band size: 6; 109 kD; Observed band size: 130 kD)

Immunohistochemical analysis of IRE1 staining in mouse kidney formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incubated with the antibody at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.

Immunofluorescent analysis of IRE1 staining in PC12 cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a hidified chamber. Cells were washed with PBST and incubated with a AF594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).