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Specifications
- Assay duration:One step
- Assay Type:Sandwich
- Reactivity:Mouse
- Sensitivity:0.112 mU/ml
- Target protein:GGT1/GGT
- Description:Mouse GGT1/GGT ELISA kit
- Format:Pre-coated
- 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:2 - 32 mU/ml
- Storage temperature:4 °C
- Sample volume:40 μl
- Regulatory status:RUO
Specifications
About this item
Mouse GGT1/GGT ELISA kit is a 90 minutes sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse GGT1/GGT in serum, plasma, and other biological fluids.
- Higher throughput: Get results in just 90 minutess, with a single wash step
- Detection Range: 2 - 32 mU/mL
- Sensitivity: 0.112 mU/ml
- Sample Type: Serum, plasma or other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Mouse GGT1/GGT ELISA kit (A311724) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse GGT1/GGT in serum, plasma or other biological fluids. An antibody specific for GGT1/GGT has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the GGT1/GGT present in each sample is bound to the wells by the immobilized antibody. Biotinylated anti-GGT1/GGT antibody, which also binds the GGT1/GGT present in each sample, and Streptavidin-HRP, which binds the Biotinylated anti-GGT1/GGT antibody, are added and the microtiter plate is incubated. Following incubation, unbound Biotinylated anti-GGT1/GGT 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 GGT1/GGT 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 GGT1/GGT 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.