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Human Interleukin-1 beta ELISA Kit

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Human Interleukin-1 beta ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Interleukin-1 beta, cu reactivitate declarată pentru Human. Măsoară în domeniul 2-400 pg/ml, are o sensibilitate de < 2 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-1 beta ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Interleukin-1 beta 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
< 2 pg/ml
Detection type
Colorimetric
Product range
2-400 pg/ml
Assay Time
3h 30m
Specificitate
This sandwich ELISA can detect both natural and recombinant human IL-1ß .
Principiul testului
This IL-1ß enzyme linked immunosorbent assay (ELISA) applies a technique called quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific to IL-1ß. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated monoclonal antibody preparation specific for IL-1ß and incubated. IL-1ß, if present, will bind and become immobilized by the antibody pre-coated on the wells and then become “sandwiched” by biotin conjugate. The microtiter plate wells are thoroughly washed to remove unbound IL-1ß and other components of the sample. In order to quantitatively determine the amount of IL-1ß present in the sample, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Avidin is a tetramer containing four identical subunits, each having a high affinity-binding site for biotin. The wells are thoroughly washed to remove all unbound HRP-conjugated Avidin 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 IL-1ß, biotin-conjugated antibody, and enzyme-conjugated Avidin 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 450 nm ± 2 nm. In order to measure the concentration of IL-1ß 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-1ß concentration (pg/mL). The concentration of IL-1ß in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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