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Human Serum Amyloid A ELISA Kit (Second Generation)

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Human Serum Amyloid A ELISA Kit (Second Generation) este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Serum Amyloid A, cu reactivitate declarată pentru Human. Măsoară în domeniul 5ng/ml-16µg/ml, are o sensibilitate de 1.1 ng/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Serum, plasma and other biological fluids. Se livrează în mărimea 96T, la prețul de 5.124,35 lei cu TVA.

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

Descriere

Human Serum Amyloid A ELISA Kit (Second Generation) is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Serum Amyloid A in serum, plasma and other biological fluids.

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Specificații

Mărime
96T
Applications
Sandwich ELISA
Reactivity
Human
Sensitivity
1.1 ng/ml
Detection type
Colorimetric
Product range
5ng/ml-16µg/ml
Assay Time
2h 30m
Specificitate
This sandwich ELISA recognises both natural and recombinant human SAA.
Principiul testului
This SAA 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 for SAA. Standards or samples are then added to the appropriate microtiter plate wells and incubated. SAA, 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 SAA and other components of sample. In order to quantitate the amount of SAA present in the sample, a standardized preparation of horseradish peroxidase (HRP)-conjugated monoclonal antibody specific for SAA is added to each well to "sandwich" the SAA 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 SAA 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 SAA in the samples, 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 SAA (ng/mL). The concentration of SAA in the samples is then determined by comparing the O.D. of the samples to the standard curve.

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