- Duur van de test:Multiple steps
- Assaytype:Sandwich
- Formaat:Pre-coated
- Primary antibody reactivity:Human
- Target protein:DNA Ligase IV/LIG4
- Omschrijving:Human DNA Ligase IV/LIG4 ELISA kit
- Monstertype:Serum, plasma, tissue homogenates, and other biological fluids
- Kruisreactiviteit:Human DNA Ligase IV/LIG4 ELISA Kit exhibits high specificity and excellent specificity for the detection of human DNA Ligase IV/LIG4. No significant cross-reactivity or interference between DNA Ligase IV/LIG4 and analogues was observed.
- Detectiemethode:Colorimetric
- Time to Results:4 hours
- Houdbaarheid:Store for 6 months at 4 °C
- Detectiebereik:0,156 - 10 ng/ml
- Opslagtemperatuur:4 °C
- Monstervolume:100 μl
- Gevoeligheid:0,094 ng/ml
- Regulatory status:RUO
- Tests per kit:96 tests
Human DNA Ligase IV/LIG4 ELISA Kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human DNA Ligase IV/LIG4 in serum, plasma, tissue homogenates, and other biological fluids.
- Ready-to-use ELISA kit
- Assay Precision: Intra-Assay: CV <8%, Inter-Assay: CV <10%
Human DNA Ligase IV/LIG4 ELISA Kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of human DNA Ligase IV/LIG4 in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for DNA Ligase IV/LIG4 has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the DNA Ligase IV/LIG4 present in each sample is bound to the wells by the immobilised antibody. Following incubation, the wells are washed and then incubated with Biotinylated Anti-DNA Ligase IV/LIG4 Antibody, which binds the captured DNA Ligase IV/LIG4 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 visualise 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 DNA Ligase IV/LIG4 captured in each well. The concentration of DNA Ligase IV/LIG4 can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.