Imagine indisponibilăRat Endothelial Lipase/LIPG ELISA Kit
Pe scurt
Rat Endothelial Lipase/LIPG ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Endothelial Lipase/LIPG, cu reactivitate declarată pentru Rat. Măsoară în domeniul 0.625-40 ng/ml, are o sensibilitate de 0.375 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
Rat Endothelial Lipase/LIPG ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat Endothelial Lipase/LIPG in serum, plasma, tissue homogenates, and other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Applications
- Sandwich ELISA
- Reactivity
- Rat
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.375 ng/ml
- Cross reactivity
- Specific for Endothelial Lipase/LIPG with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 0.625-40 ng/ml
- Assay Time
- 4 hours
- Principiul testului
- Rat Endothelial Lipase/LIPG ELISA Kit (A80288) is a 4 hour sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat Endothelial Lipase/LIPG in serum, plasma, tissue homogenates, and other biological fluids. A 96-well microtiter plate has been pre-coated with an antibody specific for Endothelial Lipase/LIPG. Standards and samples are added to the wells, where Endothelial Lipase/LIPG binds to the immobilized capture antibody. Following incubation, unbound components are removed by washing and a biotinylated detection antibody specific for Endothelial Lipase/LIPG is added to the wells. The detection antibody binds the captured Endothelial Lipase/LIPG 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 Endothelial Lipase/LIPG captured in each well. The concentration of Endothelial Lipase/LIPG is calculated by reading the absorbance at 450 nm and comparing the values with the standard curve.
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