Imagine indisponibilăHuman NF-L ELISA Kit
Pe scurt
Human NF-L ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea NF-L, cu reactivitate declarată pentru Human. Măsoară în domeniul 31.25 - 2000 pg/ml, are o sensibilitate de 8.518 pg/ml și folosește detecție Colorimetric. Se livrează în mărimea 96T, la prețul de 4.225,93 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human NF-L ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human NF-L in serum, plasma, cell culture supernates, cell lysates, tissue homogenates and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- NF-L
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 8.518 pg/ml
- Detection type
- Colorimetric
- Product range
- 31.25 - 2000 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Human NF-L ELISA Kit (A117953) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human NF-L in serum, plasma, cell culture supernates, cell lysates, tissue homogenates and other biological fluids. An antibody specific for NF-L has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the NF-L 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-NF-L Antibody, which binds the captured NF-L present in each well. Following incubation, unbound biotinylated detection antibody is removed by washing, and an HRP-Streptavidin conjugate is 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 NF-L captured in each well. The concentration of NF-L 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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