Specifications
- Pk:96 Tests
- Assay duration:Multiple steps
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:GLUT9
- Description:Mouse GLUT9 ELISA kit
- Sample type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross reactivity:Mouse GLUT9 ELISA kit exhibits high specificity and excellent specificity for the detection of mouse GLUT9. No significant cross-reactivity or interference between GLUT9 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
- Sensitivity:46,875 pg/ml
- Regulatory status:RUO
Specifications
About this item
Mouse GLUT9 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse GLUT9 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 78,125 to 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%
Mouse GLUT9 ELISA kit (A303451) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse GLUT9 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for GLUT9 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the GLUT9 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-GLUT9 antibody, which binds the captured GLUT9 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 GLUT9 captured in each well. The concentration of GLUT9 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.