Imagine indisponibilăUncoated Rat NRP2 ELISA Kit
Pe scurt
Uncoated Rat NRP2 ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea NRP2, cu reactivitate declarată pentru Rat. Măsoară în domeniul 78.13 - 5000 pg/ml, folosește detecție Colorimetric Detection (OD450) și se poate folosi pe probe de tip Serum and plasma. Se livrează în mărimea 5 x 96T, la prețul de 3.760,08 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Uncoated Rat NRP2 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay designed for the in vitro quantitative determination of rat NRP2 in serum and plasma. Uncoated ELISA kits provide the essential components required to perform ELISA assays. They are an ideal cost-effective option for experienced users who can independently establish and optimize their own ELISA systems.
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Specificații
- Brand
- Antibodies
- Mărime
- 5 x 96T
- Țintă
- NRP2
- Applications
- Sandwich ELISA
- Reactivity
- Rat
- Assay type
- Sandwich (quantitative)
- Sample type
- Serum and plasma
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 78.13 - 5000 pg/ml
- Assay Time
- 24 hours
- Principiul testului
- The Uncoated Rat NRP2 ELISA Kit (A327172) is based on a quantitative sandwich enzyme-linked immunosorbent assay (ELISA) for the detection of NRP2 in rat serum and plasma. In this format, a capture antibody specific to NRP2 is first coated onto the wells of a 96-well microtiter plate by the user. After blocking nonspecific binding sites, standards or test samples are added, and NRP2 present in the samples binds to the immobilized capture antibody. Following incubation, a biotinylated detection antibody specific for a different epitope of NRP2 is introduced, forming a capture antibody–antigen–detection antibody complex. After washing to remove unbound detection antibody, HRP–streptavidin conjugate is added, binding to the biotinylated detection antibody. Unbound conjugate is removed by washing, and TMB substrate is added. The HRP enzyme catalyzes the conversion of TMB to a blue product, which changes to yellow after the addition of an acidic stop solution. The color intensity, measured at 450 nm, is directly proportional to the concentration of NRP2 in the sample. Sample concentrations are determined by comparing their absorbance values to a standard curve generated from known NRP2 standards.
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