Specifications
- Assay duration:One step
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:IDH3A
- Description:Mouse IDH3A ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma or other biological fluids
- Detection Method:Colorimetric
- Time to Results:1 h 30 min
- Shelf Life:Store for 6 months at 4 °C
- Detection Range:75 - 1200 ng/L
- Storage Temperature:4 °C
- Sample Volume:40 μl
- Sensitivity:5.27 ng/L
- Regulatory Status:RUO
- Cat. No.:77212-960
Specifications
About this item
Mouse IDH3A ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse IDH3A in serum, plasma, and other biological fluids.
- Higher throughput: Get results in just 90 minutess, with a single wash step
- Detection Range: 75 to 1200 ng/L
- Sensitivity: 5.27 ng/L
- Sample Type: Serum, plasma or other biological fluids
- Assay precision: Intra assay: CV <8%, Inter assay: CV <10%
Mouse IDH3A ELISA kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse IDH3A in serum, plasma or other biological fluids. An antibody specific for IDH3A has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the IDH3A present in each sample is bound to the wells by the immobilized antibody. Biotinylated anti-IDH3A antibody, which also binds the IDH3A present in each sample, and Streptavidin-HRP, which binds the Biotinylated anti-IDH3A antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated anti-IDH3A antibody and unbound Streptavidin-HRP are removed by washing, and two substrate solutions are added to the wells. Color develops in proportion to the amount of IDH3A captured in each well. The color development is stopped by addition of stop solution which changes the color from blue to yellow and the intensity of the color is then measured. The concentration of IDH3A in the samples can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.