Imagine indisponibilăHuman FSH-R ELISA Kit
Pe scurt
Human FSH-R ELISA Kit este un kit ELISA de tip Competitive (quantitative) pentru măsurarea FSH-R, cu reactivitate declarată pentru Human. Măsoară în domeniul 0.312-20 ng/ml, are o sensibilitate de 0.124 ng/ml, folosește detecție Colourmetric și se poate folosi pe probe de tip Tissue homogenates, cell lysates or other biological fluids. Se livrează în mărimile 48T și 96T, la prețuri între 4.259,20 și 5.523,65 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human FSH-R ELISA Kit is a competitive Enzyme-Linked Immunosorbent Assay (cELISA) designed for the in vitro quantitative determination of human FSH-R in tissue homogenates, cell lysates or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- FSH-R
- Applications
- Competitive ELISA
- Reactivity
- Human
- Assay type
- Competitive (quantitative)
- Sensitivity
- 0.124 ng/ml
- Detection type
- Colourmetric
- Product range
- 0.312-20 ng/ml
- Assay Time
- 2h 30m
- Principiul testului
- Human FSH-R ELISA Kit (A5448) employs the competitive enzyme immunoassay technique for the quantitative measurement of human FSH-R in tissue homogenates, cell lysates or other biological fluids. The 96-well microtiter plate has been pre-coated with FSH-R antigen. During the incubation, FSH-R present in the samples or standards competes with the fixed amount of immobilized FSH-R for binding sites on the Biotinylated Anti-FSH-R Antibody. The more FSH-R present in a sample or standard, the less Biotinylated Anti-FSH-R Antibody that binds to the plate. Following incubation, unbound Biotinylated Anti-FSH-R Antibody is removed by washing, and an HRP-Avidin conjugate is added to the wells and the microtiter plate is incubated. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is inversely proportional to the amount of FSH-R present in each sample or standard. The concentration of FSH-R can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
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