Imagine indisponibilăHuman LDHD/DLD ELISA Kit
Pe scurt
Human LDHD/DLD ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea LDHD/DLD, cu reactivitate declarată pentru Human. Măsoară în domeniul 1.56 - 100 ng/ml, are o sensibilitate de 0.59 ng/ml, folosește detecție Colourmetric și se poate folosi pe probe de tip Tissue homogenates, cell lysates or other biological fluids. Se livrează în mărimile 48T și 96T, la prețuri între 4.259,20 și 5.523,65 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Human LDHD/DLD ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human LDHD/DLD in tissue homogenates, cell lysates or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- LDHD/DLD
- Applications
- Sandwich ELISA
- Reactivity
- Human
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.59 ng/ml
- Detection type
- Colourmetric
- Product range
- 1.56 - 100 ng/ml
- Assay Time
- 4h 30m
- Principiul testului
- Human LDHD/DLD ELISA Kit (A8092) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human LDHD/DLD in tissue homogenates, cell lysates or other biological fluids. An antibody specific for LDHD/DLD has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the LDHD/DLD 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-LDHD/DLD Antibody, which binds the captured LDHD/DLD 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 LDHD/DLD captured in each well. The concentration of LDHD/DLD 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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