- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Host:
- Primary antibody reactivity:Dog
- Target protein:CXCL10/IP-10
- Description:Canine CXCL10/IP-10 ELISA kit
- Environmentally Preferable:
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Canine CXCL10/IP-10 ELISA Kit exhibits high specificity and excellent specificity for the detection of canine CXCL10/IP-10. No significant cross-reactivity or interference between CXCL10/IP-10 and analogues was observed.
- Detection method:Colorimetric
- Time to Results:4 hours
- Shelf life:Store for 6 months at 4 °C
- Detection range:31,25 - 2000 pg/ml
- Storage temperature:4 °C
- Sample volume:100 μl
- Sensitivity:18,75 pg/ml
- Regulatory status:RUO
- Tests per kit:96 tests
Canine CXCL10/IP-10 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of canine CXCL10/IP-10 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Canine CXCL10/IP-10 ELISA Kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of canine CXCL10/IP-10 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for CXCL10/IP-10 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the CXCL10/IP-10 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-CXCL10/IP-10 Antibody, which binds the captured CXCL10/IP-10 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 CXCL10/IP-10 captured in each well. The concentration of CXCL10/IP-10 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.