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Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Rat
- Target protein:Fibrinogen beta chain
- Description:Rat fibrinogen beta chain ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Rat Fibrinogen beta chain ELISA Kit exhibits high specificity and excellent specificity for the detection of rat Fibrinogen beta chain. No significant cross-reactivity or interference between Fibrinogen beta 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:1,563 - 100 ng/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:0,938 ng/ml
- Regulatory status:RUO
Specifications
About this item
Rat Fibrinogen beta chain ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat Fibrinogen beta chain in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 1,563 to 100 ng/ml
- Sensitivity: 0,938 ng/ml
- Sample type: Serum, plasma, tissue homogenates and other biological fluids
- Assay precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Rat Fibrinogen beta chain ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat Fibrinogen beta chain in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Fibrinogen beta chain has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Fibrinogen beta chain 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-Fibrinogen beta chain Antibody, which binds the captured Fibrinogen beta 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 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 Fibrinogen beta chain captured in each well. The concentration of Fibrinogen beta chain can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.