Imagine indisponibilăHuman ATP2C1 ELISA Kit
Pe scurt
Human ATP2C1 ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea ATP2C1, cu reactivitate declarată pentru Human. Măsoară în domeniul 0.156-10 ng/ml, are o sensibilitate de 0.077 ng/ml și folosește detecție Colourmetric. 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 ATP2C1 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human ATP2C1 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
- ATP2C1
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.077 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
- Human ATP2C1 ELISA Kit (A82348) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human ATP2C1 in serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids. An antibody specific for ATP2C1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the ATP2C1 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-ATP2C1 Antibody, which binds the captured ATP2C1 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 ATP2C1 captured in each well. The concentration of ATP2C1 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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