Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Rat
- Target protein:GST3/GST pi
- Description:Rat GST3/GST pi ELISA kit
- Sample type:Serum, plasma, tissue homogenates and other biological fluids
- Cross reactivity:Rat GST3/GST pi ELISA Kit exhibits high specificity and excellent specificity for the detection of rat GST3/GST pi. No significant cross-reactivity or interference between GST3/GST pi 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:0,156 - 10 ng/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:0,094 ng/ml
- Regulatory status:RUO
Specifications
About this item
Rat GST3/GST pi ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat GST3/GST pi in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA Kit
- Detection range: 0,156 to 10 ng/ml
- Sensitivity: 0,094 ng/ml
- Sample type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Rat GST3/GST pi ELISA Kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat GST3/GST pi in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for GST3/GST pi has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the GST3/GST pi 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-GST3/GST pi Antibody, which binds the captured GST3/GST pi 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 GST3/GST pi captured in each well. The concentration of GST3/GST pi can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.