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Human Interferon-gamma ELISA Kit

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Human Interferon-gamma ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Interferon gamma, cu reactivitate declarată pentru Human. Măsoară în domeniul 7.5-1600 pg/ml, are o sensibilitate de 7.5 pg/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Serum, plasma, cell culture supernatant, and other biological fluids. Se livrează în mărimile 96T, 192T și 192T x 3, la prețuri între 4.625,23 și 13.143,63 lei cu TVA.

Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.

Descriere

Human Interferon-gamma ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Interferon-Gamma in serum, plasma, cell culture supernatant, and other biological fluids.

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Specificații

Mărimi disponibile
96T · 192T · 192T x 3
Applications
Sandwich ELISA
Reactivity
Human
Sensitivity
7.5 pg/ml
Detection type
Colorimetric
Product range
7.5-1600 pg/ml
Assay Time
2h 30m
Specificitate
This IFN-? ELISA Kit recognizes both natural and recombinant human IFN-?.
Principiul testului
This IFN-? enzyme-linked immunosorbent assay (ELISA) applies a technique called a quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal specific for IFN-?. Standards or samples are then added to the appropriate microtiter plate wells and incubated. IFN-?, if present, will bind and become immobilized by the antibody pre-coated on the wells. The microtiter plate wells are thoroughly washed to remove unbound IFN-? and other components of sample. In order to quantitatively determine the amount of IFN-? present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated monoclonal antibody specific for IFN-? is added to each well to "sandwich" the IFN-? immobilized during the first incubation. The microtiter plate then undergoes a second incubation. The wells are thoroughly washed to remove all unbound HRP-conjugated antibodies and 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 IFN-? and enzyme-conjugated antibody will exhibit a change in colour. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the colour change is measured spectrophotometrically at a wavelength of 450nm ± 2nm. In order to measure the concentration of IFN-? in the samples this kit contains two calibration diluents. (Calibrator Diluent I for serum/plasma testing and Calibrator Diluent II for cell culture supernatant/ urine testing). According to the testing system, the provided standard is diluted (2-fold) with the appropriate Calibrator Diluent and assayed at the same time as the samples. This allows the operator to produce a standard curve of Optical Density (O.D.) versus IFN-? concentration (pg/mL). The concentration of IFN-? in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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