Specifications
- Assay duration:Multiple steps
- Assay Type (ELISA with LOV):Sandwich
- Format:Pre-coated
- Primary antibody reactivity:Human
- Target protein:TLT-1
- Description:Human TLT-1 ELISA kit
- Size:96 tests
- Sample Type:Serum, plasma, tissue homogenates and other biological fluids
- Cross Reactivity:Human TLT-1 ELISA kit exhibits high specificity and excellent specificity for the detection of human TLT-1. No significant cross-reactivity or interference between TLT-1 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:62.5 - 4000 pg/ml
- Storage Temperature:4 °C
- Sample Volume:100 μl
- Sensitivity:37.5 pg/ml
- Regulatory Status:RUO
- Cat. No.:76737-064
Specifications
About this item
Human TLT-1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human TLT-1 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready to use ELISA kit
- Detection range: 62.5 to 4000 pg/ml
- Sensitivity: 37.5 pg/ml
- Sample type: Serum. plasma. tissue homogenates. and other biological fluids
- Assay precision: Intra assay: CV <8%. Inter assay: CV <10%
Human TLT-1 ELISA kit (A75920) employs the sandwich enzyme immunoassay technique for the quantitative measurement of human TLT-1 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for TLT-1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the TLT-1 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-TLT-1 Antibody, which binds the captured TLT-1 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 TLT-1 captured in each well. The concentration of TLT-1 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.