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Anti-Cytochrome P450 2C19 Antibody

Catalog Number: orb304733

DispatchUsually dispatched within 5-10 working days
$ 140.00
Catalog Numberorb304733
CategoryAntibodies
DescriptionRabbit polyclonal antibody to Cytochrome (phospho-450 2C19)
Species/HostRabbit
ClonalityPolyclonal
Tested applicationsIF, IH, WB
ReactivityHuman, Primate
ImmunogenKLH-conjugated synthetic peptide encompassing a sequence within the center region of human Cytochrome P450 2C19. The exact sequence is proprietary.
Antibody TypePrimary Antibody
Dilution rangeWB: 1:500-1000, IHC-P: 1:100-200, IF/ICC: 1:100-500
Form/AppearanceLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
ConjugationUnconjugated
TargetCYP2C19
Entrez1557
UniProt IDP33261
SourceRabbit
StorageMaintain 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.
Buffer/PreservativesLiquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.
Alternative namesanti Cytochrome P450 2C19 antibody, anti (R)-limon
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NoteFor research use only
Expiration Date12 months from date of receipt.
Anti-Cytochrome P450 2C19 Antibody

Western blot analysis of Cytochrome P450 2C19 expression in HepG2 (A), SGC7901 (B) whole cell lysates. (Predicted band size: 55 kD; Observed band size: 56 kD)

Anti-Cytochrome P450 2C19 Antibody

Immunohistochemical analysis of Cytochrome P450 2C19 staining in human brain 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.

Anti-Cytochrome P450 2C19 Antibody

Immunofluorescent analysis of Cytochrome P450 2C19 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 DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

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