Imagine indisponibilăRat PDGF AA ELISA Kit
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Rat PDGF AA ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea PDGF AA, cu reactivitate declarată pentru Rat. Măsoară în domeniul 0.78-50 pg/ml, are o sensibilitate de 0.47 pg/ml, folosește detecție Colorimetric Detection (OD450) și se poate folosi pe probe de tip Serum, plasma and other biological fluids. Se livrează în mărimea 96T, la prețul de 3.826,63 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Rat PDGF AA ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay designed for the in vitro quantitative determination of rat PDGF AA in serum, plasma, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- PDGF AA
- Applications
- Sandwich ELISA
- Reactivity
- Rat
- Recommended dilutions
- The suggested dilution for serum/plasma is 10-100 fold.
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.47 pg/ml
- Sample type
- Serum, plasma and other biological fluids.
- Cross reactivity
- Specific for PDGF-AA with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 0.78-50 pg/ml
- Assay Time
- 3h 30m
- Principiul testului
- Rat PDGF AA ELISA Kit (A327027) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat PDGF AA in serum, plasma, and other biological fluids. An antibody specific for PDGF AA has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the PDGF AA present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-PDGF AA Antibody, which binds the captured PDGF AA present in each well. Following incubation, unbound biotinylated detection antibody is removed by washing, and an HRP-Streptavidin conjugate is added to the wells and the microtiter plate is incubated. Following incubation and washing, 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 proportional to the amount of PDGF AA captured in each well. The concentration of PDGF AA 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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