2007
DOI: 10.1038/nprot.2007.100
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Rapid measurement of total antioxidant capacity in plants

Abstract: There is growing interest in measuring the antioxidant status of plant tissues. This protocol describes the oxygen radical absorbance capacity (ORAC) assay, which measures antioxidant inhibition of peroxyl radical-induced oxidations and is a measure of total antioxidant capacity. The assay is performed in a microplate and is assessed with a 96-well multi-detection plate reader. Total antioxidant capacity of 64 experimental samples can easily be analyzed in 1 d. This assay is presented along with rapid assays f… Show more

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Cited by 204 publications
(142 citation statements)
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“…Immediately after each A/C i curve was completed, tissue was removed from the leaf using a cork borer and flash frozen in liquid N. One leaf disc (approximately 1.4 cm 2 ) was incubated in 96% (v/v) ethanol for 3 d at 4°C in order to determine chlorophyll content using the equations of Lichtenthaler and Wellburn (1983). Another leaf disc was used to determine the ORAC content following the procedures described by Gillespie et al (2007). A third leaf disc was used to determine Suc content according to the methods of Jones et al (1977).…”
Section: Gold Standard Methods For Measuring Leaf Physiology and Biocmentioning
confidence: 99%
“…Immediately after each A/C i curve was completed, tissue was removed from the leaf using a cork borer and flash frozen in liquid N. One leaf disc (approximately 1.4 cm 2 ) was incubated in 96% (v/v) ethanol for 3 d at 4°C in order to determine chlorophyll content using the equations of Lichtenthaler and Wellburn (1983). Another leaf disc was used to determine the ORAC content following the procedures described by Gillespie et al (2007). A third leaf disc was used to determine Suc content according to the methods of Jones et al (1977).…”
Section: Gold Standard Methods For Measuring Leaf Physiology and Biocmentioning
confidence: 99%
“…Antioxidant capacity of cold tea extract and hot tea extracts was also assessed conducting the ORAC (oxygen radical absorbance capacity) assay, according to the method proposed by Gillespie et al, (14). The initial samples with a concentration of 10000 ppm were diluted in PBS (phosphate buffered saline) 75 mM for cold tea extracts, the dilutions were made as follows: 1:50 for Jaibel The diluted samples were added to 96-well-microplates; 187 μL of fluorescein (80 nM) diluted in PBS (75 mM) were also added to each well.…”
Section: Orac Assaymentioning
confidence: 99%
“…ORAC assay for AA-2G, AA-2G, and AA was carried out as described by Gillespie et al, 21) with a slight modification. Briefly, fluorescein (60 nM), antioxidant (12.5 mM), and AAPH (18.75 mM) were incubated in 200 ml of KH 2 PO 4 -K 2 HPO 4 buffer (75 mM, pH 7.0) at 37 C in a 96-well plate (Costar no.…”
Section: Abtsmentioning
confidence: 99%