E04N0670 Rabbit NAD(P)H dehydrogenase [quinone] 1 ELISA kit
Rabbit NAD(P)H dehydrogenase [quinone] 1 ELISA kit is suitable for detecting samples from rabbit species. NAD(P)H dehydrogenase [quinone] 1 can also be called DHQU, DIA4, DTD, NMOR1, NMORI, QR1, Azoreductase, DT-diaphorase, Menadione reductase, Phylloquinone reductase, Quinone reductase 1, NAD(P)H:quinone oxidoreductase 1, NQO1, NQO 1.
Product Information | |
Cat. No. | E04N0670 |
Product Name | Rabbit NAD(P)H dehydrogenase [quinone] 1 ELISA kit |
Species | Rabbit |
Product Size | 48 Tests / 96 Tests |
Concentration | 1.0-25ng/mL |
Sensitivity | 0.1 ng/mL |
Principal | Competitive ELISA |
Sample Volume | 100 ul |
Sample Type | Serum, plasma, cell culture supernatants, body fluid and tissue homogenate |
Assay Time | 90 minutes |
Platform | Microplate Reader |
Conjugate | HRP |
Detection Method | Colorimetric |
Storage | 2-8°C |
Kit Components | ||
MATERIALS | SPECIFICATION | QUANTITY |
MICROTITER PLATE | 96 wells | stripwell |
ENZYME CONJUGATE | 6.0 mL | 1 vial |
STANDARD A (0.5mL) | 0 ng/mL | 1 vial |
STANDARD B (0.5mL) | 1.0 ng/mL | 1 vial |
STANDARD C (0.5mL) | 2.5 ng/mL | 1 vial |
STANDARD D (0.5mL) | 5.0 ng/mL | 1 vial |
STANDARD E (0.5mL) | 10 ng/mL | 1 vial |
STANDARD F (0.5mL) | 25 ng/mL | 1 vial |
SUBSTRATE A | 6 mL | 1 vial |
SUBSTRATE B | 6 mL | 1 vial |
STOP SOLUTION | 6 mL | 1 vial |
WASH SOLUTION (100 x) | 10 mL | 1 vial |
BALANCE SOLUTION | 3 mL | 1 vial |
Principle of the Assay |
NQO1 ELISA kit applies the competitive enzyme immunoassay technique utilizing an anti- NQO1 antibody and an NQO1-HRP conjugate. The assay sample and buffer are incubated together with NQO1-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 NQO1 concentration since NQO1 from samples and NQO1-HRP conjugate compete for the anti-NQO1 antibody binding site. Since the number of sites is limited, as more sites are occupied by NQO1 from the sample, fewer sites are left to bind NQO1-HRP conjugate. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The NQO1 concentration in each sample is interpolated from this standard curve. |
Coefficient of Variance | Intra Variation% ＜10% | |
Inter Variation% ＜12% | ||
Recovery | 89-114.79% | |
Linearity | Diluent Ratio | Range % |
1:2 | 96-116 | |
1:4 | 91-109 | |
1:8 | 88-103 | |
Specificity/Cross-reactivity | No significant cross-reactivity or interference between NQO1 and analogues was observed. | |
![Summary of the Assay Procedure for Rabbit NAD(P)H dehydrogenase [quinone] 1 ELISA kit](/uploads/image/20230331/14/e04a0204-human-tnf-alpha-elisa-kit.webp "Summary of the Assay Procedure for Rabbit NAD(P)H dehydrogenase [quinone] 1 ELISA kit")
E04N0670 has been referenced in the below publications:
The Nrf2-ARE Pathway Is Associated With Schisandrin B Attenuating Benzo(a)pyrene_x005fInduced HTR Cells Damages in Vitro.
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