Imagine indisponibilăHuman uPAR ELISA Kit
Pe scurt
Human uPAR ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea uPAR, cu reactivitate declarată pentru Human. Măsoară în domeniul 62.5-4000 pg/ml, are o sensibilitate de < 4 pg/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Serum, plasma, body fluids, tissue lysates, and cell culture supernatants. 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 uPAR ELISA Kit is a sandwhich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human uPAR in serum, plasma, body fluids, tissue lysates, and cell culture supernatants.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- uPAR
- Applications
- Sandwhich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- < 4 pg/ml
- Detection type
- Colorimetric
- Platform
- Microplate
- Product range
- 62.5-4000 pg/ml
- Principiul testului
- This uPAR enzyme linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate has been pre-coated with an Anti-uPAR Antibody. Standards or samples are then added to the microtire plate wells and uPAR, if present, will bind to the antibody pre-coated on the wells. In order to quantify the amount of uPAR present in the sample, Anti-uPAR Antibody (Biotin) is added to each well to "sandwich" the uPAR immobilised on the plate. The microtiter plate then undergoes incubation, followed by thorough washing of the wells to remove all unbound components. Next, Avidin-Biotin-Peroxidase Complex is added to each well for a short incubation period, followed by thorough washing of the wells to remove all unbound conjugates. Next, a TMB (3,3',5,5' tetramethyl-benzidine) substrate solution is added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain uPAR will exhibit a change in colour. The enzyme-substrate reaction is terminated by the addition of a stop solution and the colour change is measured spectrophotometrically at a wavelength of 450nm ± 2nm.
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