Imagine indisponibilăRat Malondialdehyde ELISA Kit
Pe scurt
Rat Malondialdehyde ELISA Kit este un kit ELISA de tip Competitive (quantitative) pentru măsurarea Malondialdehyde, cu reactivitate declarată pentru Rat. Măsoară în domeniul 7.813-500 ng/ml, are o sensibilitate de 4.688 ng/ml, folosește detecție Colorimetric Detection (OD450) și se poate folosi pe probe de tip Serum, plasma, tissue homogenates, and other biological fluids. Se livrează în mărimea 96T, la prețul de 3.993,00 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Rat Malondialdehyde ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of rat Malondialdehyde in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- Malondialdehyde
- Applications
- Competitive ELISA
- Reactivity
- Rat
- Assay type
- Competitive (quantitative)
- Sensitivity
- 4.688 ng/ml
- Cross reactivity
- Specific for Malondialdehyde with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 7.813-500 ng/ml
- Assay Time
- 2 hours
- Principiul testului
- Rat Malondialdehyde ELISA Kit (A247177) is a 2 hour competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of rat Malondialdehyde in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with Malondialdehyde. During the assay, Malondialdehyde present in the standards or samples competes with immobilized Malondialdehyde for binding to an assay-specific antibody. Following incubation, unbound components are removed by washing and HRP-Streptavidin conjugate is added to the wells. After further incubation and washing, TMB substrate solution is added to visualize the HRP enzymatic reaction. This produces a blue-coloured product that changes to yellow following addition of acidic stop solution. The intensity of the colour is measured at 450 nm using a microplate reader. The concentration of Malondialdehyde in the samples is inversely proportional to the OD450 value and is determined by comparison with the standard curve.
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