Imagine indisponibilăMouse TNF-Related Activation-induced Cytokine ELISA Kit
Pe scurt
Mouse TNF-Related Activation-induced Cytokine ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea TNF-Related Activation-induced Cytokine, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 31.25 - 2000 pg/ml, are o sensibilitate de 4.23 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
Mouse TNF-Related Activation-induced Cytokine ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse TNF-Related Activation-induced Cytokine in cell culture supernatant, serum and plasma.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 4.23 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
- 31.25 - 2000 pg/ml
- Specificitate
- This kit can assay both native and recombinant mouse TRANCE.
- Principiul testului
- Mouse TRANCE ELISA Kit is based on the quantitative sandwich enzyme-linked immunosorbent assay technique to measure concentration of mouse TRANCE in the samples. A monoclonal antibody specific for mouse TRANCE has been immobilized onto microwells. Standard or samples are pipetted into the wells, followed by the addition of biotin-linked monoclonal antibody specific for TRANCE, and TRANCE 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 TRANCE 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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