Imagine indisponibilăRabbit Myelin Basic Protein ELISA Kit
Pe scurt
Rabbit Myelin Basic Protein ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea Myelin Basic Protein, cu reactivitate declarată pentru Rabbit. Măsoară în domeniul 0.156-10 ng/ml, are o sensibilitate de 0.055 ng/ml, folosește detecție Colourmetric și se poate folosi pe probe de tip Serum, plasma or other biological fluids. Se livrează în mărimile 48T și 96T, la prețuri între 4.225,93 și 5.457,10 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Rabbit Myelin Basic Protein ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rabbit Myelin Basic Protein in serum, plasma or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- Myelin Basic Protein
- Applications
- Sandwich ELISA
- Reactivity
- Rabbit
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.055 ng/ml
- Sample type
- Serum, plasma or other biological fluids.
- Detection type
- Colourmetric
- Product range
- 0.156-10 ng/ml
- Assay Time
- 4h 30m
- Principiul testului
- Rabbit Myelin Basic Protein ELISA Kit (A8004) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rabbit Myelin Basic Protein in serum, plasma or other biological fluids. An antibody specific for Myelin Basic Protein has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Myelin Basic Protein 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-Myelin Basic Protein Antibody, which binds the captured Myelin Basic Protein 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 Myelin Basic Protein captured in each well. The concentration of Myelin Basic Protein 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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