Imagine indisponibilăHuman Cardiac Troponin I ELISA Kit
Pe scurt
Human Cardiac Troponin I ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Cardiac Troponin I, cu reactivitate declarată pentru Human. Măsoară în domeniul 312-20,000 pg/ml, are o sensibilitate de < 10 pg/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Serum, cell culture supernatants, and tissue homogenates. 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
Human Cardiac Troponin I ELISA Kit is a sandwhich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Cardiac Troponin I in serum, cell culture supernatants, and tissue homogenates.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- Cardiac Troponin I
- Applications
- Sandwhich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- < 10 pg/ml
- Detection type
- Colorimetric
- Platform
- Microplate
- Product range
- 312-20,000 pg/ml
- Principiul testului
- This Cardiac Troponin I enzyme linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate has been pre-coated with an Anti-Cardiac Troponin I Antibody. Standards or samples are then added to the microtire plate wells and Cardiac Troponin I, if present, will bind to the antibody pre-coated on the wells. In order to quantify the amount of Cardiac Troponin I present in the sample, Anti-Cardiac Troponin I Antibody (HRP) is added to each well to "sandwich" the Cardiac Troponin I immobilised on the plate. The microtiter plate then undergoes incubation, followed by thorough washing of the wells to remove all unbound components. 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 Cardiac Troponin I 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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