Imagine indisponibilăMouse SDHB ELISA Kit
Pe scurt
Mouse SDHB ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea SDHB, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 0.156-10 ng/ml, are o sensibilitate de 0.053 ng/ml, folosește detecție Colourmetric și se poate folosi pe probe de tip Tissue homogenates or other biological fluids. Se livrează în mărimile 48T și 96T, la prețuri între 4.325,75 și 5.656,75 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Mouse SDHB ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse SDHB in tissue homogenates or other biological fluids.
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Specificații
- Brand
- Antibodies
- Mărimi disponibile
- 48T · 96T
- Țintă
- SDHB
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 0.053 ng/ml
- Detection type
- Colourmetric
- Product range
- 0.156-10 ng/ml
- Assay Time
- 4h 30m
- Principiul testului
- Mouse SDHB ELISA Kit (A8041) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse SDHB in tissue homogenates or other biological fluids. An antibody specific for SDHB has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the SDHB 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-SDHB Antibody, which binds the captured SDHB 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 SDHB captured in each well. The concentration of SDHB 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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