- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Chicken
- Target protein:Fibrinogen alpha Chain
- Description:Chicken fibrinogen alpha chain ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Chicken Fibrinogen alpha Chain ELISA kit exhibits high specificity and excellent specificity for the detection of chicken Fibrinogen alpha Chain. No significant cross-reactivity or interference between Fibrinogen alpha Chain and analogues was observed.
- Detection Method:Colorimetric
- Time to Results:4 h 30 min
- Assay Principle:Quantitative
- Shelf Life:Store for 6 months at 4 °C
- Detection Range:15.625 - 1000 pg/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:9.375 pg/ml
- Regulatory Status:RUO
- Cat. No.:76729-876
Chicken Fibrinogen alpha Chain ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of chicken Fibrinogen alpha Chain in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 15.625 to 1000 pg/ml
- Sensitivity: 9.375 pg/ml
- Sample type: Serum. plasma. tissue homogenates. and other biological fluids
- Assay precision: Intra assay: CV <8%. Inter assay: CV <10%
Chicken Fibrinogen alpha Chain ELISA kit (A76040) employs the sandwich enzyme immunoassay technique for the quantitative measurement of chicken Fibrinogen alpha Chain in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Fibrinogen alpha Chain has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Fibrinogen alpha Chain 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-Fibrinogen alpha Chain Antibody, which binds the captured Fibrinogen alpha Chain 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 Fibrinogen alpha Chain captured in each well. The concentration of Fibrinogen alpha Chain can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.