Imagine indisponibilăMouse ATM ELISA Kit
Pe scurt
Mouse ATM ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea ATM, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 7.813-500 pg/ml, are o sensibilitate de 4.688 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 4.392,30 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse ATM ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse ATM in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- ATM
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 4.688 pg/ml
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 7.813-500 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Mouse ATM ELISA Kit (A77722) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse ATM in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for ATM. Standards and samples are added to the wells, where ATM binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for ATM is added to the wells. The detection antibody binds the captured ATM 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 ATM captured in each well. The concentration of ATM is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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