Imagine indisponibilăHuman IL-1 alpha ELISA Kit
Pe scurt
Human IL-1 alpha ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea IL-1 alpha, cu reactivitate declarată pentru Human. Măsoară în domeniul 7.81 - 500 pg/ml, are o sensibilitate de 1.26 pg/ml și folosește detecție Colorimetric. 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 alpha ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human IL-1 alpha in serum, plasma, cell culture supernates, cell lysates, tissue homogenates and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- IL-1 alpha
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 1.26 pg/ml
- Detection type
- Colorimetric
- Product range
- 7.81 - 500 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Human IL-1 alpha ELISA Kit (A117476) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human IL-1 alpha in serum, plasma, cell culture supernates, cell lysates, tissue homogenates and other biological fluids. An antibody specific for IL-1 alpha has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the IL-1 alpha 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 alpha Antibody, which binds the captured IL-1 alpha 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 alpha captured in each well. The concentration of IL-1 alpha 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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