Imagine indisponibilăMouse FSH-R ELISA Kit
Pe scurt
Mouse FSH-R ELISA Kit este un kit ELISA de tip Competitive (quantitative) pentru măsurarea FSH-R, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 2.344-150 mIU/mL (53 ng = 150 mIU), are o sensibilitate de 1.406 mIU/ml, folosește detecție Colorimetric Detection (OD450) și se poate folosi pe probe de tip Serum, plasma, tissue homogenates, and other biological fluids. 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
Mouse FSH-R ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of mouse FSH-R in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- FSH-R
- Applications
- Competitive ELISA
- Reactivity
- Mouse
- Assay type
- Competitive (quantitative)
- Sensitivity
- 1.406 mIU/ml
- Cross reactivity
- Specific for FSH-R with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 2.344-150 mIU/mL (53 ng = 150 mIU)
- Assay Time
- 2 hours
- Principiul testului
- Mouse FSH-R ELISA Kit (A78102) is a 2 hour competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of mouse FSH-R in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with FSH-R. During the assay, FSH-R present in the standards or samples competes with immobilized FSH-R for binding to an assay-specific antibody. Following incubation, unbound components are removed by washing and HRP-Streptavidin conjugate is added to the wells. After further incubation and washing, TMB substrate solution is added to visualize the HRP enzymatic reaction. This produces a blue-coloured product that changes to yellow following addition of acidic stop solution. The intensity of the colour is measured at 450 nm using a microplate reader. The concentration of FSH-R in the samples is inversely proportional to the OD450 value and is determined by comparison with the standard curve.
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