Specifications
- Assay duration:One step
- Assay Type:Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:CTLA4
- Description:Mouse CTLA4 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:1.25 - 20 ng/ml
- Storage temperature:4 °C
- Sample volume:40 μl
- Sensitivity:0.058 ng/ml
- Regulatory status:RUO
- Cat. no.:77211-876
Specifications
About this item
Mouse CTLA4 ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse CTLA4 in serum, plasma, and other biological fluids.
- Higher throughput: Get results in just 90 minutess, with a single wash step
- Detection Range: 1.25 - 20 ng/mL
- Sensitivity: 0.058 ng/ml
- Sample Type: Serum, plasma or other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Mouse CTLA4 ELISA kit (A312575) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse CTLA4 in serum, plasma or other biological fluids. An antibody specific for CTLA4 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the CTLA4 present in each sample is bound to the wells by the immobilized antibody. Biotinylated anti-CTLA4 antibody, which also binds the CTLA4 present in each sample, and Streptavidin-HRP, which binds the Biotinylated anti-CTLA4 antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated anti-CTLA4 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 CTLA4 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 CTLA4 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.