Imagine indisponibilăMouse MAP1A ELISA Kit
Pe scurt
Mouse MAP1A ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea MAP1A, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 0.156-10 ng/ml, are o sensibilitate de 0.07 ng/ml și folosește detecție Colourmetric. Se livrează în mărimile 48T și 96T, la prețuri între 3.993,00 și 5.290,73 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse MAP1A ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse MAP1A in serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- MAP1A
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.07 ng/ml
- Sample type
- Serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
- Detection type
- Colourmetric
- Product range
- 0.156-10 ng/ml
- Assay Time
- 4h 30m
- Principiul testului
- Mouse MAP1A ELISA Kit (A3982) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse MAP1A in serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids. An antibody specific for MAP1A has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the MAP1A 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-MAP1A Antibody, which binds the captured MAP1A 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 MAP1A captured in each well. The concentration of MAP1A 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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