Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Rat
- Target protein:Amyloid Precursor Protein
- Description:Rat amyloid Precursor Protein ELISA kit
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Rat Amyloid Precursor Protein ELISA Kit exhibits high specificity and excellent specificity for the detection of rat Amyloid Precursor Protein. No significant cross-reactivity or interference between Amyloid Precursor Protein 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
- Sensitivity:9,375 pg/ml
- Regulatory status:RUO
Specifications
About this item
Rat amyloid precursor protein ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat amyloid precursor protein in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Rat Amyloid Precursor Protein ELISA kit (A303736) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat Amyloid Precursor Protein in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Amyloid Precursor Protein has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Amyloid Precursor Protein 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-Amyloid Precursor Protein antibody, which binds the captured Amyloid Precursor Protein 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 Amyloid Precursor Protein captured in each well. The concentration of Amyloid Precursor Protein can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.