Imagine indisponibilăHorse AMH ELISA Kit
Pe scurt
Horse AMH ELISA Kit este un kit ELISA de tip Competitive (quantitative) pentru măsurarea AMH, cu reactivitate declarată pentru Horse. Măsoară în domeniul 0.156-10 ng/ml, are o sensibilitate de 0.094 ng/ml și folosește detecție Colorimetric Detection (OD450). Se livrează în mărimea 96T, la prețul de 4.957,98 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Horse AMH ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of horse AMH in serum, plasma, cell culture supernatant, cell or tissue lysate, and other liquid samples.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- AMH
- Applications
- Competitive ELISA
- Reactivity
- Horse
- Assay type
- Competitive (quantitative)
- Sensitivity
- 0.094 ng/ml
- Sample type
- Serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 0.156-10 ng/ml
- Assay Time
- 2 hours
- Principiul testului
- Horse AMH ELISA Kit (High Sensitivity) (A326343) is a 2 hour competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of horse AMH in serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids. A 96-well microtiter plate has been pre-coated with AMH. During the assay, AMH present in the standards or samples competes with immobilized AMH 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 AMH in the samples is inversely proportional to the OD450 value and is determined by comparison with the standard curve.
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