Imagine indisponibilăRat IL2 ELISA Kit
Pe scurt
Rat IL2 ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea IL2, cu reactivitate declarată pentru Rat. Măsoară în domeniul 31.2-2000 pg/ml, are o sensibilitate de < 1 pg/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Serum, body fluids, tissue lysates, and cell culture supernatants. Se livrează în mărimea 96T, la prețul de 3.726,80 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Rat IL2 ELISA Kit is a sandwhich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat IL2 in serum, body fluids, tissue lysates, and cell culture supernatants.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- IL2
- Applications
- Sandwhich ELISA
- Reactivity
- Rat
- Assay type
- Sandwich (quantitative)
- Sensitivity
- < 1 pg/ml
- Detection type
- Colorimetric
- Platform
- Microplate
- Product range
- 31.2-2000 pg/ml
- Principiul testului
- This IL2 enzyme linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate has been pre-coated with an Anti-IL2 Antibody. Standards or samples are then added to the microtire plate wells and IL2, if present, will bind to the antibody pre-coated on the wells. In order to quantify the amount of IL2 present in the sample, Anti-IL2 Antibody (Biotin) is added to each well to "sandwich" the IL2 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 IL2 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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