Imagine indisponibilăHuman Leptin ELISA Kit
Pe scurt
Human Leptin ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Leptin, cu reactivitate declarată pentru Human. Măsoară în domeniul 15-1000 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 Leptin ELISA Kit is a Sandwich Enzyme-Linked Immunosorbent Assay designed for the indirect in vitro quantitative determination of Leptin levels in plasma, serum, and lysates.
Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- Leptin
- 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
- 15-1000 pg/ml
- Principiul testului
- This Human Leptin ELISA Kit allows for the quantitative determination of natural or recombinant Leptin within any experimental sample including cell lysates, serum, and plasma. This Human Leptin 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 Leptin. Standards or samples are then added to the appropriate microtiter plate wells and incubated. If present, Leptin will bind and become immobilized by the antibody pre-coated on the wells. Leptin then becomes “sandwiched” by the primary capture antibodies and the secondary detection antibodies subsequently added. After incubation and “sandwiching” of Leptin, 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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