Imagine indisponibilăHuman LRG1 ELISA Kit
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Human LRG1 ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea LRG1, cu reactivitate declarată pentru Human. Măsoară în domeniul 31.25 - 2000 pg/ml, are o sensibilitate de 10.13 pg/ml, folosește detecție Colorimetric și se poate folosi pe probe de tip Serum, plasma and cell culture supernates. Se livrează în mărimea 96T, la prețul de 4.225,93 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human LRG1 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human LRG1 in serum, plasma and cell culture supernates.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- LRG1
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 10.13 pg/ml
- Sample type
- Serum, plasma and cell culture supernates.
- Detection type
- Colorimetric
- Product range
- 31.25 - 2000 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Human LRG1 ELISA Kit (A120168) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human LRG1 in serum, plasma and cell culture supernates. An antibody specific for LRG1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the LRG1 present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-LRG1 Antibody, which binds the captured LRG1 present in each well. Following incubation, unbound biotinylated detection antibody is removed by washing, and an HRP-Streptavidin conjugate is added to the wells and the microtiter plate is incubated. Following incubation and washing, TMB substrate solution is then used to visualize the HRP enzymatic reaction by catalysis to produce a blue-coloured product that changes to yellow after addition of acidic stop solution. The density of yellow is proportional to the amount of LRG1 captured in each well. The concentration of LRG1 can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.
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