Imagine indisponibilăHuman P-Selectin ELISA Kit
Pe scurt
Human P-Selectin ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea P Selectin, cu reactivitate declarată pentru Human. Măsoară în domeniul 78.13 - 5000 pg/ml, are o sensibilitate de 1.11 pg/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Cell culture supernatant, serum and plasma. Se livrează în mărimea 96T, la prețul de 3.726,80 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human P-Selectin ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human P-Selectin in cell culture supernatant, serum and plasma.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- P Selectin
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 1.11 pg/ml
- Sample type
- Cell culture supernatant, serum and plasma.
- Cross reactivity
- This ELISA kit has shown no significant cross-reactivity.
- Detection type
- Colorimetric
- Platform
- Microplate
- Product range
- 78.13 - 5000 pg/ml
- Specificitate
- This kit can assay both native and recombinant human P-Selectin.
- Principiul testului
- Human P-Selectin ELISA Kit is based on the quantitative sandwich enzyme-linked immunosorbent assay technique to measure concentration of human sP-Selectin in the samples. A monoclonal antibody specific for human sP-Selectin has been immobilized onto microwells. Standard or samples are pipetted into the wells, followed by the addition of biotin-linked monoclonal antibody specific for sP-Selectin, and sP-Selectin present is bound by the immobilized antibody and detect antibody following the first incubation. After removal of any unbound substances, streptavidin-HRP is added for a second incubation. After washing, substrate solution reacts with HRP and color develops in proportion to the amount of sP-Selectin bound by the immobilized antibody. The color development is stopped by addition of acid and the optical density value is measured by microplate reader.
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