Imagine indisponibilăMouse Cystatin A ELISA Kit
Pe scurt
Mouse Cystatin A ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Cystatin A, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 46.8-3000 pg/ml, are o sensibilitate de 14.25 pg/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 Cystatin A ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Cystatin A in serum, plasma, saliva, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- Cystatin A
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 14.25 pg/ml
- Detection type
- Colourmetric
- Product range
- 46.8-3000 pg/ml
- Assay Time
- 4h 30m
- Principiul testului
- Mouse Cystatin A ELISA Kit (A7843) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Cystatin A in serum, plasma, saliva, tissue homogenates, cell lysates, cell culture supernates or other biological fluids. An antibody specific for Cystatin A has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Cystatin 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-Cystatin A Antibody, which binds the captured Cystatin 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 Cystatin A captured in each well. The concentration of Cystatin 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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