Imagine indisponibilăChicken ABP1 ELISA Kit
Pe scurt
Chicken ABP1 ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea ABP1, cu reactivitate declarată pentru Chicken. Măsoară în domeniul 1.563-100 ng/ml, are o sensibilitate de 0.938 ng/ml și folosește detecție Colorimetric Detection (OD450). Se livrează în mărimea 96T, la prețul de 4.625,23 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Chicken ABP1 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of chicken ABP1 in serum, plasma, cell culture supernatant, cell or tissue lysate, and other liquid samples.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- ABP1
- Applications
- Sandwich ELISA
- Reactivity
- Chicken
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.938 ng/ml
- Sample type
- Serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 1.563-100 ng/ml
- Assay Time
- 4 hours
- Principiul testului
- Chicken ABP1 ELISA Kit (A334896) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of chicken ABP1 in serum, plasma, cell culture supernatant, cell or tissue lysate, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for ABP1. Standards and samples are added to the wells, where ABP1 binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for ABP1 is added to the wells. The detection antibody binds the captured ABP1 to form an antibody-antigen-antibody sandwich complex. After further incubation and washing, HRP-Streptavidin conjugate is added to the wells. TMB substrate solution is then 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 yellow colour is directly proportional to the amount of ABP1 captured in each well. The concentration of ABP1 is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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