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Human Interleukin-16 ELISA Kit

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Human Interleukin-16 ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Interleukin-16, cu reactivitate declarată pentru Human. Măsoară în domeniul 20-3200 pg/ml, are o sensibilitate de < 20 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 Interleukin-16 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Interleukin-16 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
< 20 pg/ml
Detection type
Colorimetric
Product range
20-3200 pg/ml
Assay Time
4h 30m
Specificitate
This sandwich ELISA recognizes both natural and recombinant human IL-16.
Principiul testului
This IL-16 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 antibody specific for IL-16. Standards or samples are then added to the appropriate microtiter plate wells and incubated. IL-16, if present, will bind and become immobilized by the antibody pre-coated on the wells. The microtiter plate wells are thoroughly washed to remove any unbound IL-16 and other components of sample. In order to quantitatively determine the amount of IL-16 present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated monoclonal antibody specific for IL-16 is added to each well to "sandwich" the IL-16 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 solution are allowed to react over a short incubation period. Only those wells that contain IL-16 and enzyme-substrate reaction will exhibit a change in colour. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the colour change measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. In order to measure the concentration of IL-16 in the samples, this kit includes two calibration diluents (Calibrator Diluent I for serum/plasma testing and Calibrator Diluent II for cell culture supernatant 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 IL-16 (pg/mL). The concentration of IL-16 in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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