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Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:Tissue Plasminogen Activator
- Description:Mouse Tissue Plasminogen Activator ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Mouse Tissue Plasminogen Activator ELISA Kit exhibits high specificity and excellent specificity for the detection of mouse Tissue Plasminogen Activator. No significant cross-reactivity or interference between Tissue Plasminogen Activator 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:39,063 - 2500 pg/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:23,438 pg/ml
- Regulatory status:RUO
Specifications
About this item
Mouse Tissue Plasminogen Activator ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse Tissue Plasminogen Activator in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA Kit
- Detection Range: 39,063 to 2500 pg/ml
- Sensitivity: 23,438 pg/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Mouse Tissue Plasminogen Activator ELISA Kit (A78908) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse Tissue Plasminogen Activator in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for Tissue Plasminogen Activator has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the Tissue Plasminogen Activator 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-Tissue Plasminogen Activator Antibody, which binds the captured Tissue Plasminogen Activator 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 Tissue Plasminogen Activator captured in each well. The concentration of Tissue Plasminogen Activator can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.