Imagine indisponibilăHuman Cancer Antigen 242 ELISA Kit
Pe scurt
Human Cancer Antigen 242 ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Cancer Antigen 242, cu reactivitate declarată pentru Human. Măsoară în domeniul 31.25 - 2000 pg/ml, are o sensibilitate de 18.75 pg/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 4.591,95 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human Cancer Antigen 242 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Cancer Antigen 242 in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- Cancer Antigen 242
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 18.75 pg/ml
- Cross reactivity
- Specific for Cancer Antigen 242 with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 31.25 - 2000 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Human Cancer Antigen 242 ELISA Kit (A302607) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Cancer Antigen 242 in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for Cancer Antigen 242. Standards and samples are added to the wells, where Cancer Antigen 242 binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for Cancer Antigen 242 is added to the wells. The detection antibody binds the captured Cancer Antigen 242 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 Cancer Antigen 242 captured in each well. The concentration of Cancer Antigen 242 is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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