Imagine indisponibilăHuman Eotaxin ELISA Kit
Pe scurt
Human Eotaxin ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Eotaxin, cu reactivitate declarată pentru Human. Măsoară în domeniul 11-750 pg/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Plasma, serum, and lysates. Se livrează în mărimea 96T, la prețul de 3.993,00 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human Eotaxin ELISA Kit is a Sandwich Enzyme-Linked Immunosorbent Assay designed for the indirect in vitro quantitative determination of Eotaxin levels in plasma, serum, and lysates.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- Eotaxin
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sample type
- Plasma, serum, and lysates.
- Cross reactivity
- No reported cross-reactivity.
- Detection type
- Colorimetric
- Product range
- 11-750 pg/ml
- Principiul testului
- This Human Eotaxin ELISA Kit allows for the quantitative determination of natural or recombinant Eotaxin within any experimental sample including cell lysates, serum, and plasma. This Human Eotaxin ELISA Kit applies a technique called quantitative sandwich immunoassay. The microtiter plate provided in this kit has been pre-coated with a monoclonal antibody specific for Eotaxin. Standards or samples are then added to the appropriate microtiter plate wells and incubated. If present, Eotaxin will bind and become immobilized by the antibody pre-coated on the wells. Eotaxin then becomes “sandwiched” by the primary capture antibodies and the secondary detection antibodies subsequently added. After incubation and “sandwiching” of Eotaxin, a peroxidase enzyme is conjugated to the constant heavy chain of the secondary antibody (either covalently or via Avidin/Streptavidin-Biotin interactions), allowing for a colorimetric reaction to ensue upon substrate addition. When the substrate TMB (3, 3’, 5, 5’-Tetramethylbenzidine) is added, the reaction catalyzed by peroxidase yields a blue color that is representative of the antigen concentration. Upon sufficient color development, the reaction can be terminated through addition of Stop Solution (2 N Sulfuric Acid) where the color of the solution will turn yellow. The absorbance of each well can then be read by a spectrophotometer, allowing for generation of a standard curve and subsequent determination of protein concentration.
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