Imagine indisponibilăNitroimidazole ELISA Kit
Pe scurt
Nitroimidazole ELISA Kit este un kit ELISA de tip Competitive (quantitative) pentru măsurarea Nitroimidazole. Folosește detecție Colorimetric și se poate folosi pe probe de tip Tissue (chicken, duck, liver, fish, shrimp), egg, honey. Se livrează în mărimea 96T, la prețul de 2.562,18 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Nitroimidazole ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of Nitroimidazole in tissue (chicken, duck, liver, fish, shrimp), egg, honey.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- Nitroimidazole
- Applications
- Competitive ELISA
- Assay type
- Competitive (quantitative)
- Detection type
- Colorimetric
- Assay Time
- <5 hours
- Recovery
- 75-115%
- Principiul testului
- Nitroimidazole ELISA Test Kit (A327234) employs the competitive enzyme immunoassay technique for the quantitative measurement of Nitroimidazole in tissue (chicken, duck, liver, fish, shrimp), egg, honey. The 96-well microtiter plate has been pre-coated with Nitroimidazole. During the incubation, Nitroimidazole present in the samples or standards competes with the fixed amount of immobilized Nitroimidazole for binding sites of the Anti-Nitroimidazole Antibody, a HRP-Conjugated Secondary Antibody is added to the wells at the same time. The more Nitroimidazole present in a sample or standard, the less Anti-Nitroimidazole Antibody that binds to the plate. Following incubation, unbound HRP-Conjugated Secondary Antibody is removed by washing. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is inversely proportional to the amount of Nitroimidazole present in each sample or standard. The concentration of Nitroimidazole can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
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