Imagine indisponibilăHuman MYPN ELISA Kit
Pe scurt
Human MYPN ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea MYPN, cu reactivitate declarată pentru Human. Măsoară în domeniul 0.156-10 ng/ml, are o sensibilitate de 0.047 ng/ml, folosește detecție Colourmetric și se poate folosi pe probe de tip Tissue homogenates or other biological fluids. Se livrează în mărimile 48T și 96T, la prețuri între 4.259,20 și 5.523,65 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human MYPN ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human MYPN in tissue homogenates or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- MYPN
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.047 ng/ml
- Detection type
- Colourmetric
- Product range
- 0.156-10 ng/ml
- Assay Time
- 4h 30m
- Principiul testului
- Human MYPN ELISA Kit (A5235) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human MYPN in tissue homogenates or other biological fluids. An antibody specific for MYPN has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the MYPN 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-MYPN Antibody, which binds the captured MYPN 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 MYPN captured in each well. The concentration of MYPN 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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