Imagine indisponibilăMouse LDL ELISA Kit
Pe scurt
Mouse LDL ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea LDL, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 7.813-500 ng/ml, are o sensibilitate de 4.688 ng/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 3.993,00 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse LDL ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse LDL in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- LDL
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 4.688 ng/ml
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 7.813-500 ng/ml
- Assay Time
- 4 hours
- Principiul testului
- Mouse LDL ELISA Kit (A78376) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse LDL in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for LDL. Standards and samples are added to the wells, where LDL binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for LDL is added to the wells. The detection antibody binds the captured LDL 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 LDL captured in each well. The concentration of LDL is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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