Imagine indisponibilăGoat, Sheep LBP ELISA Kit
Pe scurt
Goat, Sheep LBP ELISA Kit este un kit ELISA de tip Competitive (quantitative) pentru măsurarea LBP, cu reactivitate declarată pentru Goat, Sheep. Măsoară în domeniul 62.5-4000 ng/ml, are o sensibilitate de 37.5 ng/ml și folosește detecție Colorimetric Detection (OD450). Se livrează în mărimea 96T, la prețul de 4.625,23 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Goat, Sheep LBP ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of goat, sheep LBP in serum, plasma, cell culture supernatant, cell or tissue lysate, and other liquid samples.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- LBP
- Applications
- Competitive ELISA
- Reactivity
- Goat, Sheep
- Assay type
- Competitive (quantitative)
- Sensitivity
- 37.5 ng/ml
- Sample type
- Serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 62.5-4000 ng/ml
- Assay Time
- 2 hours
- Principiul testului
- Goat, Sheep LBP ELISA Kit (A334905) is a 2 hour competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of sheep, goat LBP in serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids. A 96-well microtiter plate has been pre-coated with LBP. During the assay, LBP present in the standards or samples competes with immobilized LBP 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 LBP in the samples is inversely proportional to the OD450 value and is determined by comparison with the standard curve.
Documentație
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