2005
DOI: 10.1186/1472-6750-5-12
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A simple technique for quantifying apoptosis in 96-well plates

Abstract: Background: Analyzing apoptosis has been an integral component of many biological studies. However, currently available methods for quantifying apoptosis have various limitations including multiple, sometimes cell-damaging steps, the inability to quantify live, necrotic and apoptotic cells at the same time, and non-specific detection (i.e. "false positive"). To overcome the shortcomings of current methods that quantify apoptosis in vitro and to take advantage of the 96-well plate format, we present here a modi… Show more

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Cited by 641 publications
(294 citation statements)
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References 27 publications
(13 reference statements)
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“…Determination of apoptosis and necrosis by acridine orange/ethidium bromide double staining -fluorescence microscopy analyses Acridine orange/ethidium bromide (AO/EB) double staining was performed according to Ribble et al [37]. AO and EB are DNA-binding fluorescent dyes.…”
Section: Assessment Of Mitochondrial Membrane Potential (δψM)mentioning
confidence: 99%
“…Determination of apoptosis and necrosis by acridine orange/ethidium bromide double staining -fluorescence microscopy analyses Acridine orange/ethidium bromide (AO/EB) double staining was performed according to Ribble et al [37]. AO and EB are DNA-binding fluorescent dyes.…”
Section: Assessment Of Mitochondrial Membrane Potential (δψM)mentioning
confidence: 99%
“…10 l of each sample was dotted on a glass slide, covered with a coverslip, and counted using ϫ180 magnification on a Nikon SM1500 fluorescent microscope per Ref. 19. A minimum of 200 cells were counted per point, and grouped into four categories based on nuclear morphology and stain: viable (green with intact nuclei), necrotic (orange with intact nuclei), early apoptotic with intact membrane (green with fragmented nuclei), and late apoptotic with damaged membrane (orange with fragmented nuclei).…”
Section: Apoptosis Assays and Caspase Inhibitor Treatmentmentioning
confidence: 99%
“…Cell viability staining assay of the pneumococcal biofilm by acridine orange and ethidium bromide: To assess the effects of potential compounds on bacterial cell viability, an acridine orange/ethidium bromide staining assay was done according to the standard method [37,38]. The acridine orange/ethidium bromide reagent was made by mixing of 100 µg/mL of ethidium bromide and 100 µg/mL of acridine orange in PBS.…”
Section: Antimicrobial Activity By Agar Well Diffusion Methodmentioning
confidence: 99%