Imagine indisponibilăMouse VLDL ELISA Kit
Pe scurt
Mouse VLDL ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea VLDL, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 0.781-50 ng/ml, are o sensibilitate de 0.469 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 4.392,30 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse VLDL ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse VLDL in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- VLDL
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.469 ng/ml
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 0.781-50 ng/ml
- Assay Time
- 4 hours
- Principiul testului
- Mouse VLDL ELISA Kit (A87407) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse VLDL in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for VLDL. Standards and samples are added to the wells, where VLDL binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for VLDL is added to the wells. The detection antibody binds the captured VLDL 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 VLDL captured in each well. The concentration of VLDL is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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