Imagine indisponibilăMouse G-CSF ELISA Kit
Pe scurt
Mouse G-CSF ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea G-CSF, cu reactivitate declarată pentru Mouse. Măsoară în domeniul 7.8-500 pg/ml, are o sensibilitate de 2.9 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
Mouse G-CSF ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse G-CSF in serum, plasma and cell culture supernates.
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Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- G-CSF
- Applications
- Sandwich ELISA
- Reactivity
- Mouse
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 2.9 pg/ml
- Sample type
- Serum, plasma and cell culture supernates.
- Detection type
- Colorimetric
- Product range
- 7.8-500 pg/ml
- Assay Time
- 4 hours
- Principiul testului
- Mouse G-CSF ELISA Kit (A117490) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse G-CSF in serum, plasma and cell culture supernates. An antibody specific for G-CSF has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the G-CSF 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-G-CSF Antibody, which binds the captured G-CSF 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 G-CSF captured in each well. The concentration of G-CSF 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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