Imagine indisponibilăHuman IL-1 beta ELISA Kit
Pe scurt
Human IL-1 beta ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea IL-1 beta, cu reactivitate declarată pentru Human. Măsoară în domeniul 6.25-400 pg/ml, are o sensibilitate de 3.9 pg/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Serum, plasma and cell culture supernates. Se livrează în mărimea 96T, la prețul de 4.225,93 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human IL-1 beta ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human IL-1 beta in serum, plasma and cell culture supernates.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- IL-1 beta
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 3.9 pg/ml
- Sample type
- Serum, plasma and cell culture supernates.
- Detection type
- Colorimetric
- Product range
- 6.25-400 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Human IL-1 beta ELISA Kit (A117448) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human IL-1 beta in serum, plasma and cell culture supernates. An antibody specific for IL-1 beta has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the IL-1 beta present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-IL-1 beta Antibody, which binds the captured IL-1 beta present in each well. Following incubation, unbound biotinylated detection antibody is removed by washing, and an HRP-Streptavidin conjugate is added to the wells and the microtiter plate is incubated. 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 proportional to the amount of IL-1 beta captured in each well. The concentration of IL-1 beta 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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