Human CYP2B1 ELISA Kit

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  • Alternative name

    Cytochrome P450 2B1 ELISA KIT; CYPIIB1 ELISA KIT; Cytochrome P450-B ELISA KIT; Cytochrome P450b ELISA KIT; Cytochrome P450-LM2 ELISA KIT; Cytochrome P450-PB1 ELISA KIT; Cytochrome P450-PB2Cyp2b1 ELISA KIT; Cyp2b-1 ELISA KIT; Cytochrome P450b ELISA KIT

  • Catalog
    E011041
  • species
    Human
  • GeneCYP2B1
  • Standard CurveHuman CYP2B1 ELISA Kit
  • Other Species Mouse CYP2B1 ELISA KitRat Cyp2b1 ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseHuman CYP2B1 ELISA Kit allows for the in vitro quantitative determination of CYP2B1 , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageFor 5-7days:Store the whole kit at 4℃
    For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
  • Product Description
    specifical
    For samples: Serum, plasma, cell culture supernatants, body fluid and tissue homogenate INTENDED USE This CYP2B1 ELISA kit is a 1.5 hour solid-phase ELISA designed for the quantitative determination of Human CYP2B1. This ELISA kit for research use only, not for therapeutic or diagnostic applications! PRINCIPLE OF THE ASSAY CYP2B1 ELISA kit applies the competitive enzyme immunoassay technique utilizing a monoclonal anti-CYP2B1 antibody and an CYP2B1-HRP conjugate. The assay sample and buffer are incubated together with CYP2B1-HRP conjugate in pre-coated plate for one hour. After the incubation period, the wells are decanted and washed five times. The wells are then incubated with a substrate for HRP enzyme. The product of the enzyme-substrate reaction forms a blue colored complex. Finally, a stop solution is added to stop the reaction, which will then turn the solution yellow. The intensity of color is measured spectrophotometrically at 450nm in a microplate reader. The intensity of the color is inversely proportional to the CYP2B1 concentration since CYP2B1 from samples and CYP2B1-HRP conjugate compete for the anti-CYP2B1 antibody binding site. Since the number of sites is limited, as more sites are occupied by CYP2B1 from the sample, fewer sites are left to bind CYP2B1-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The CYP2B1 concentration in each sample is interpolated from this standard curve.



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