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For research use only.
Detection Principle | Fe3+ can be deoxidized to Fe2+ by VE with ferroin existing. Fe2+ can react with phenanthroline and form pink compound under certain condition. After colorimetric assay, VE content can be figured out according to the standard curve or calculated through formula. |
Synonyms | VE |
Sample Type | Serum,Plasma,Tissue |
Detection Method | Colorimetric method |
Detection Instrument | Microplate reader (525-533 nm, optimum wavelength: 533 nm) |
Research Area | Oxidative Stress, Plant Physiology Series |
Other Reagents Required | Normal saline (0.9% NaCl), PBS (0.01 mol/L, pH 7.4), Absolute ethanol, N-heptane |
Storage | This product can be stored at 2-8°C for 12 months with shading light. |
Valid Period | 12 months |
Sensitivity | 0.95 μg/mL |
Detection Range | 0.95-40 μg/mL |
Precision | inter-assay CV: 6.3% | intra-assay CV: 3.9% |
Sample Volume | 0.15 mL |
Assay Time | 30 min |
The recommended dilution factor for different samples is as follows (for reference only):
Sample Type | Dilution Factor |
---|---|
Human serum | 1 |
Mouse serum | 1 |
Chicken serum | 1 |
10% Mouse liver tissue homogenate | 1 |
10% Mouse brain tissue homogenate | 1 |
10% Rat kidney tissue homogenate | 1 |
10% Rat lung tissue homogenate | 1 |
10% Rat spleen tissue homogenate | 1 |
10% Rat heart tissue homogenate | 1 |
The diluent is normal saline (0.9% NaCl) or PBS (0.01 M, pH 7.4). For the dilution of other sample types, please do pretest to confirm the dilution factor.
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