Specifications
- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Rat
- Target protein:IGFBP5
- Description:Rat IGFBP5 ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Rat IGFBP5 ELISA kit exhibits high specificity and excellent specificity for the detection of rat IGFBP5. No significant cross-reactivity or interference between IGFBP5 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:78.125 - 5000 pg/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:46.875 pg/ml
- Regulatory Status:RUO
- Cat. No.:76737-552
Specifications
About this item
Rat IGFBP5 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of rat IGFBP5 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-To-Use ELISA Kit
- Detection Range: 78.125 - 5000 pg/ml
- Sensitivity: 46.875 pg/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Rat IGFBP5 ELISA kit (A76757) employs the sandwich enzyme immunoassay technique for the quantitative measurement of rat IGFBP5 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for IGFBP5 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the IGFBP5 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-IGFBP5 Antibody, which binds the captured IGFBP5 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 IGFBP5 captured in each well. The concentration of IGFBP5 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.