Specifications
- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:CTP Synthase/CTPS
- Description:Human CTP synthase/CTPS ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates, and other biological fluids
- Cross Reactivity:Human CTP Synthase/CTPS ELISA Kit exhibits high specificity and excellent specificity for the detection of human CTP Synthase/CTPS. No significant cross-reactivity or interference between CTP Synthase/CTPS 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:31.25 - 2000 pg/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:18.75 pg/ml
- Regulatory Status:RUO
- Cat. No.:76739-640
Specifications
About this item
Human CTP Synthase/CTPS ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human CTP Synthase/CTPS in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Detection Range: 31.25 - 2000 pg/ml
- Sensitivity: 18.75 pg/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Human CTP Synthase/CTPS ELISA kit (A302864) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human CTP Synthase/CTPS in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for CTP Synthase/CTPS has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the CTP Synthase/CTPS present in each sample is bound to the wells by the immobilized antibody. Following incubation, the wells are washed and then incubated with Biotinylated anti-CTP Synthase/CTPS antibody, which binds the captured CTP Synthase/CTPS 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 visualize 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 CTP Synthase/CTPS captured in each well. The concentration of CTP Synthase/CTPS can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.