NA/NE (Noradrenaline/Norepinephrine) ELISA Kit
Target Information | |
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Target Name | NA/NE (Noradrenaline/Norepinephrine) |
Synonyms | Norepinephrine, NE, noradrenaline, NA, NAd, norad, 4, 5-β-trihydroxyphenethylamine |
Product Properties | |
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Prize | Online Inquiry |
Reactivity | Universal |
Assay Type | Competitive-ELISA |
Assay Time | 2.0 h |
Detection Range | 0.31-20 ng/mL |
Sample Type | Serum, plasma and other biological fluids |
Sample Volume | 50 μL |
Sensitivity | 0.19 ng/mL |
Specificity | This kit recognizes NA/NE in samples. No significant cross-reactivity or interference between NA/NE and analogues was observed. |
Research Area | Cardiovascular, Neuroscience |
Reproducibility | Both intra-CV and inter-CV are < 10%. |
Precision | Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level NA/NE were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level NA/NE were tested on 3 different plates, 20 replicates in each plate. |
Storage | -20 ℃. Please refer to the instructions for details. |
Application
This ELISA kit applies to the in vitro quantitative determination of NA/NE concentrations in serum, plasma and other biological fluids.
Test Principle
This ELISA kit uses the Competitive-ELISA principle. The micro ELISA plate provided in this kit has been pre-coated with NA/NE. During the reaction, NA/NE in the sample or standard competes with a fixed amount of NA/NE on the solid phase supporter for sites on the Biotinylated Detection Ab specific to NA/NE. Excess conjugate and unbound sample or standard are washed away, and Avidin-Horseradish Peroxidase (HRP) conjugate are added to each micro plate well and incubated. Then a TMB substrate solution is added to each well. The enzyme-substrate reaction is terminated by the addition of stop solution and the color turns from blue to yellow. The optical density (OD) is measured spectrophotometrically at a wavelength of 450 nm ± 2 nm. The concentration of NA/NE in tested samples can be calculated by comparing the OD of the samples to the standard curve.
! For research use only. Not intended for any clinical use.