Anti-Cytochrome P450 2C8/9/18/19 Antibody

• Catalog Number: orb665762
• Category: Antibodies
• Description: Rabbit polyclonal antibody to Cytochrome P450 2C8/9/18/19
• Target: CYP2C8; CYP2C9; CYP2C18; CYP2C19
• Clonality: Polyclonal
• Species/Host: Rabbit
• Conjugation: Unconjugated
• Reactivity: Human, Mouse, Primate, 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.
• Immunogen: KLH-conjugated synthetic peptide encompassing a sequence within the center region of human Cytochrome P450 2C8/9/18/19. The exact sequence is proprietary.
• UniProt ID: P11712, P33261, P33260, P10632
• Tested applications: IF, IH, WB
• Dilution range: WB: 1-500-1000, IHC-P: 1-50-200, IF: 1-100-500
• 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: Anti-CYP2C8 antibody, anti-Cytochrome P450 2C8 ant
• Note: For research use only
• Entrez: 1558, 1562, 1557, 1559

Western blot analysis of Cytochrome P450 2C8/9/18/19 expression in rat liver (A) whole cell lysates. (Predicted band size: 55 kD; Observed band size: 56 kD)

Immunohistochemical analysis of Cytochrome P450 2C8/9/18/19 staining in human liver cancer 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 Cytochrome P450 2C8/9/18/19 staining in HeLa 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 Alexa Fluor 594-conjugated secondary antibody (red) in PBS at room temperature in the dark.