Imagine indisponibilăRat IgG2c ELISA Kit
Pe scurt
Rat IgG2c ELISA Kit este un kit ELISA de tip Sandwich (quantitative) pentru măsurarea IgG2c, cu reactivitate declarată pentru Rat. Măsoară în domeniul 6.25-400 pg/ml, are o sensibilitate de 3.75 pg/ml, folosește detecție Colorimetric Detection (OD450) și se poate folosi pe probe de tip Serum, plasma and other biological fluids. Se livrează în mărimea 96T, la prețul de 3.826,63 lei cu TVA.
Produse destinate exclusiv cercetării. Nu se utilizează în diagnostic sau tratament.
Descriere
Rat IgG2c ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay designed for the in vitro quantitative determination of rat IgG2c in serum, plasma, and other biological fluids.
Specificații
- Brand
- Antibodies
- Mărime
- 96T
- Țintă
- IgG2c
- Applications
- Sandwich ELISA
- Reactivity
- Rat
- Recommended dilutions
- The suggested dilution for serum/plasma is 400,000-2,000,000 fold.
- Assay type
- Sandwich (quantitative)
- Sensitivity
- 3.75 pg/ml
- Sample type
- Serum, plasma and other biological fluids.
- Cross reactivity
- Specific for IgG2c with no reported cross-reactivity with other analogs or variants.
- Detection type
- Colorimetric Detection (OD450)
- Product range
- 6.25-400 pg/ml
- Assay Time
- 3h 30m
- Principiul testului
- Rat IgG2c ELISA Kit (A327119) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat IgG2c in serum, plasma, and other biological fluids. An antibody specific for IgG2c has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the IgG2c 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-IgG2c Antibody, which binds the captured IgG2c 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, 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 IgG2c captured in each well. The concentration of IgG2c 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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