Imagine indisponibilăMouse Endothelin 2/ET-2 ELISA Kit
Pe scurt
Mouse Endothelin 2/ET-2 ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Endothelin 2/ET-2, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 31.2-2000 pg/ml, are o sensibilitate de 11.2 pg/ml, folosește detecție Colourmetric și se poate folosi pe probe de tip Serum, plasma or other biological fluids. Se livrează în mărimile 48T și 96T, la prețuri între 4.259,20 și 5.989,50 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse Endothelin 2/ET-2 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Endothelin 2/ET-2 in serum, plasma or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- Endothelin 2/ET-2
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 11.2 pg/ml
- Sample type
- Serum, plasma or other biological fluids.
- Detection type
- Colourmetric
- Product range
- 31.2-2000 pg/ml
- Assay Time
- 4h 30m
- Principiul testului
- Mouse Endothelin 2/ET-2 ELISA Kit (A326144) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Endothelin 2/ET-2 in serum, plasma or other biological fluids. An antibody specific for Endothelin 2/ET-2 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Endothelin 2/ET-2 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-Endothelin 2/ET-2 Antibody, which binds the captured Endothelin 2/ET-2 present in each well. HRP-Avidin conjugate is then 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 Endothelin 2/ET-2 captured in each well. The concentration of Endothelin 2/ET-2 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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