Imagine indisponibilăHuman EGF ELISA Kit
Pe scurt
Human EGF ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea EGF, cu reactivitate declarată pentru Human. Măsoară în domeniul 4.7-300 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 4.225,93 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human EGF ELISA Kit is a sandwhich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human EGF in serum, body fluids, tissue lysates, and cell culture supernatants.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- EGF
- Applications
- Sandwhich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- < 1 pg/ml
- Detection type
- Colorimetric
- Platform
- Microplate
- Product range
- 4.7-300 pg/ml
- Principiul testului
- This EGF enzyme linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate has been pre-coated with an Anti-EGF Antibody. Standards or samples are then added to the microtire plate wells and EGF, if present, will bind to the antibody pre-coated on the wells. In order to quantify the amount of EGF present in the sample, Anti-EGF Antibody (Biotin) is added to each well to "sandwich" the EGF 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 EGF 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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