Specifications
- Förp.:96 Tests
- Analysens varaktighet:Multiple steps
- Analystyp:Sandwich
- Formatera:Pre-coated
- Primary antibody reactivity:Human
- Target protein:nNOS (neuronal)
- Beskrivning:Human nNOS (neuronal) ELISA kit
- Typ av prov:Serum, plasma, tissue homogenates and other biological fluids
- Korsreaktivitet:Human nNOS (neuronal) ELISA Kit exhibits high specificity and excellent specificity for the detection of human nNOS (neuronal). No significant cross-reactivity or interference between nNOS (neuronal) 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
Specifications
About this item
Human nNOS (neuronal) ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human nNOS (neuronal) 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%
Human nNOS ELISA Kit employs the sandwich enzyme immunoassay technique for the quantitative measurement of human nNOS in serum, plasma, tissue homogenates, and other biological fluids. An antibody specific for nNOS has been pre-coated onto a 96-well microtiter plate. The standards and test samples are added into the wells and the nNOS 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-nNOS Antibody, which binds the captured nNOS 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 nNOS captured in each well. The concentration of nNOS can then be calculated by reading the O.D. absorbance at 450 nm in a microplate reader and referring to the standard curve.