Imagine indisponibilăHuman Albumin ELISA Kit
Pe scurt
Human Albumin ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Albumin, cu reactivitate declarată pentru Human. Măsoară în domeniul 15.6-1000 ng/ml, are o sensibilitate de 5.8 ng/ml și folosește detecție Colourmetric. Se livrează în mărimile 48T și 96T, la prețuri între 2.994,75 și 3.826,63 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human Albumin ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Albumin in serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- Albumin
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 5.8 ng/ml
- Sample type
- Serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids.
- Detection type
- Colourmetric
- Product range
- 15.6-1000 ng/ml
- Assay Time
- 4h 30m
- Principiul testului
- Human Albumin ELISA Kit (A2153) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human Albumin in serum, plasma, tissue homogenates, cell lysates, cell culture supernates or other biological fluids. An antibody specific for Albumin has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Albumin 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-Albumin Antibody, which binds the captured Albumin present in each well. HRP-Avidin conjugate is then 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 Albumin captured in each well. The concentration of Albumin 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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