Specifications
- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Rat
- Target protein:UCN2/SRP
- Description:Rat UCN2/SRP ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Rat UCN2/SRP ELISA Kit exhibits high specificity and excellent specificity for the detection of rat UCN2/SRP. No significant cross-reactivity or interference between UCN2/SRP 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:6.25 - 400 pg/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:3.75 pg/ml
- Regulatory Status:RUO
- Cat. No.:76738-376
Specifications
About this item
Rat UCN2/SRP ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat UCN2/SRP in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA kit
- Detection Range: 6.25 to 400 pg/ml
- Sensitivity: 3.75 pg/ml
- Sample Type: Serum, plasma, tissue homogenates and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Rat UCN2/SRP ELISA kit (A80232) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat UCN2/SRP in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for UCN2/SRP has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the UCN2/SRP 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-UCN2/SRP Antibody, which binds the captured UCN2/SRP 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 UCN2/SRP captured in each well. The concentration of UCN2/SRP can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.