Imagine indisponibilăSubstance P ELISA Kit
Pe scurt
Substance P ELISA Kit este un kit ELISA de tip Competitive (quantitative) pentru măsurarea Substance P, cu reactivitate declarată pentru Universal. Măsoară în domeniul 78.13 - 5000 pg/ml, are o sensibilitate de 46.88 pg/ml, folosește detecție Colorimetric Detection (OD450) și se poate folosi pe probe de tip Serum, plasma and other biological fluids. Se livrează în mărimea 96T, la prețul de 3.227,68 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Substance P ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay designed for the in vitro quantitative determination of Substance P in serum, plasma, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- Substance P
- Applications
- Competitive ELISA
- Reactivity
- Universal
- Assay type
- Competitive (quantitative)
- Sensitivity
- 46.88 pg/ml
- Sample type
- Serum, plasma and other biological fluids.
- Cross reactivity
- Specific for Substance P with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 78.13 - 5000 pg/ml
- Assay Time
- 2 hours
- Principiul testului
- Substance P ELISA Kit (A326981) employs the competitive enzyme immunoassay technique for the quantitative measurement of Substance P in serum, plasma, and other biological fluids. The 96-well microtiter plate has been pre-coated with Substance P antigen. During the incubation, Substance P present in the samples or standards competes with the fixed amount of immobilized Substance P for binding sites on the Biotinylated Anti-Substance P Antibody. The more Substance P present in a sample or standard, the less Biotinylated Anti-Substance P Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-Substance P 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 inversely proportional to the amount of Substance P present in each sample or standard. The concentration of Substance P 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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