Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:Semaphorin 7a
- Description:Mouse semaphorin 7a ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Mouse Semaphorin 7a ELISA kit exhibits high specificity and excellent specificity for the detection of mouse Semaphorin 7a. No significant cross-reactivity or interference between Semaphorin 7a 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:0,313 - 20 ng/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:0,188 ng/ml
- Regulatory status:RUO
Specifications
About this item
Mouse Semaphorin 7a ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Semaphorin 7a in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Detection range: 0,313 to 20 ng/ml
- Sensitivity: 0,188 ng/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Mouse Semaphorin 7a ELISA kit (A74988) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Semaphorin 7a in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Semaphorin 7a has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Semaphorin 7a 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-Semaphorin 7a Antibody, which binds the captured Semaphorin 7a 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 Semaphorin 7a captured in each well. The concentration of Semaphorin 7a can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.