Imagine indisponibilăMouse Granzyme A ELISA Kit
Pe scurt
Mouse Granzyme A ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Granzyme A, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 0.156-10 ng/ml, are o sensibilitate de 0.058 ng/ml, folosește detecție Colourmetric și se poate folosi pe probe de tip Serum, plasma, tissue homogenates, cell lysates or other biological fluids. 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 Granzyme A ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Granzyme A in serum, plasma, tissue homogenates, cell lysates or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- Granzyme A
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.058 ng/ml
- Detection type
- Colourmetric
- Product range
- 0.156-10 ng/ml
- Assay Time
- 4h 30m
- Principiul testului
- Mouse Granzyme A ELISA Kit (A2027) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Granzyme A in serum, plasma, tissue homogenates, cell lysates or other biological fluids. An antibody specific for Granzyme A has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Granzyme A 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-Granzyme A Antibody, which binds the captured Granzyme A 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 Granzyme A captured in each well. The concentration of Granzyme A 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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