Acridine Orange is used for fluorescence microscopy and flow cytometry analysis of cellular physiology and cell cycle status. This cell-permeant cellular stain can be utilized in conjunction with a number of other staining techniques and fluorogenic substrates including the Magic Red line of fluorogenic protease substrates. Acridine Orange is a useful bacteria stain for the fluorescent microscopic examination of microorganisms.
- AO may be used neat or diluted in diH2O, PBS, or media. ICT’s AO is supplied at 0.5 mL liquid at 1 mM (266 µg/mL). 2. Add AO to the cell sample media at 0.5-5 µM, equal to a final dilution of 1:2,000 – 1:200 in the cells (.05-.5% v/v). For example, if using AO at 1.0 µM in the final cell suspension, it must be diluted 1:1,000. First dilute it 1:100 in PBS or diH2O; e.g., put 10 µL AO into 990 µL PBS or diH2O. Pipette the diluted AO into the cell suspension at approximately 1:10; e.g., put 50 µL diluted AO into 450 µL cell suspension.
- Incubate 15-30 minutes at 37°C.
- Wash cells if reagent is too bright.
- Analyze with fluorescence. Lysosomes will appear yellowish green by illuminating cells with a blue light (488 nm) excitation filter and a green light (540-550 nm) emission/barrier filter. Alternatively, lysosomes will appear red when using an excitation filter of 550 nm (540-560 nm) and a long pass >610 nm emission/barrier filter.
Product Specific References
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|35429112||Duarte, C, et al. 2022. Crosstalk between dihydroceramides produced by Porphyromonas gingivalis and host lysosomal cathepsin B in the promotion of osteoclastogenesis. Journal of cellular and molecular medicine .|
|35654241||Kim, NY, et al. 2022. Tanshinone IIA exerts autophagic cell death through down-regulation of β-catenin in renal cell carcinoma cells. Biochimie.|