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Inhibition and Production of Superoxide Anionic Colorimetric Assay Kit(WST-1 Method) (E-BC-K001-M)

All Size Price Qty
96T $ 280.00
48T $ 200.00
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For research use only.

Detection Principle Superoxide anion free radicals are produced through the reaction system of xanthine and xanthine oxidase. WST-1 (a water-soluble tetrazolium salt) can react with the generated superoxide anion to produce water-soluble formazan. When the tested sample contains the superoxide anion free radical inhibitor, it can inhibit the formation of formazan. When the tested sample contains the substance that produces superoxide anion free radical, it can promote the formation of formazan dye. By colorimetric analysis of WST-1 products, the units of activity of inhibition or production of superoxide anion radical in samples can be calculated.
Sample Type Serum,Plasma,Urine,Cell,Cell culture supernatant,leucocyte
Detection Method Colorimetric method
Detection Instrument Microplate reader (440-460 nm, optimum wavelength: 450 nm)
Research Area Oxidative Stress ,  Ferroptosis
Other Reagents Required Normal saline (0.9% NaCl), PBS (0.01 mol/L, pH 7.4)
Storage This product can be stored at 2-8°C/-20°C for 12 months with shading light. Please refer to the manual for the specific storage condition of the components.
Valid Period 12 months
Precision inter-assay CV: 5.8% | intra-assay CV: 0.02
Assay Time 35 min

The recommended dilution factor for different samples is as follows (for reference only):

Sample Type Dilution Factor
Human serum 4-7
Mouse serum 15-25
Rat serum 25-35
Human saliva 1
HepG2 culture supernatant 1
10% Rat brain tissue homogenate 150-200
10% Rat liver tissue homogenate 500-600
10% Mouse liver tissue homogenate 500-600
10% Mouse heart tissue homogenate 150-200
10% Epipremnum aureum tissue homogenate 20-30

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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