Specifikationer
- Förp.:96 Tests
- Analysens varaktighet:Multiple steps
- Analystyp:Sandwich
- Formatera:Pre-coated
- Primary antibody reactivity:Mouse
- Target protein:TIE1
- Beskrivning:Mouse TIE1 ELISA kit
- Typ av prov:Serum, plasma, tissue homogenates and other biological fluids
- Korsreaktivitet:Mouse TIE1 ELISA Kit exhibits high specificity and excellent specificity for the detection of mouse TIE1. No significant cross-reactivity or interference between TIE1 and analogues was observed.
- Detektionsmetod:Colorimetric
- Time to Results:4 h 30 min
- Analysprincip:Quantitative
- Hållbarhetstid:Store for 6 months at 4 °C
- Detektionsområde:0,156 - 10 ng/ml
- Förvaringstemperatur:4 °C
- Provvolym:100 μl
- Känslighet:0,094 ng/ml
- Regulatory status:RUO
Specifikationer
Om denna produkt
Mouse TIE1 ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of mouse TIE1 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready To Use ELISA Kit
- Detection Range: 0,156 to 10 ng/ml
- Sensitivity: 0,094 ng/ml
- Sample Type: Serum, plasma, tissue homogenates, and other biological fluids
- Assay Precision: Intra - Assay: CV <8%, Inter - Assay: CV <10%
Mouse TIE1 ELISA Kit (A78876) employs the sandwich enzyme immunoassay technique for the quantitative measurement of mouse TIE1 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for TIE1 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the TIE1 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-TIE1 Antibody, which binds the captured TIE1 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 TIE1 captured in each well. The concentration of TIE1 can then be calculated by reading the O.D. absorbance at 450nm in a microplate reader and referring to the standard curve.