Specifications
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Host:
- Primary antibody reactivity:Guinea pig
- Target protein:Complement C3b
- Description:Guinea Pig Complement C3b ELISA kit
- Environmentally Preferable:
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Guinea Pig Complement C3b ELISA Kit exhibits high specificity and excellent specificity for the detection of guinea pig Complement C3b. No significant cross-reactivity or interference between Complement C3b and analogues was observed.
- Detection method:Colorimetric
- Time to Results:4 hours
- Shelf life:Store for 6 months at 4 °C
- Detection range:31,25 - 2000 pg/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:18,75 pg/ml
- Regulatory status:RUO
- Tests per kit:96 tests
Specifications
About this item
Guinea Pig Complement C3b ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of guinea pig Complement C3b in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Guinea Pig Complement C3b ELISA Kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of guinea pig Complement C3b in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Complement C3b has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Complement C3b present in each sample is bound to the wells by the immobilised antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-Complement C3b Antibody, which binds the captured Complement C3b 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 visualise 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 Complement C3b captured in each well. The concentration of Complement C3b can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.