- Regulatory Status
- Other Names
- Viability dye, dead cell exclusion dye, cell viability dye
- Ave. Rating
- Submit a Review
- Product Citations
|Cat #||Size||Price||Quantity Check Availability||Save|
|420403||200 tests||28 CHF|
|420404||500 tests||55 CHF|
7-AAD (7-amino-actinomycin D) has a high DNA binding constant and is efficiently excluded by intact cells. It is useful for DNA analysis and dead cell discrimination during flow cytometric analysis. When excited by 488 laser light, 7-AAD fluorescence is detected in the far red range of the spectrum (650 nm long-pass filter).Product Details
- PBS, pH 7.2 with 0.09% (w/v) sodium azide.
- CAUTION: 7-AAD is a potential carcinogen. It is recommended that the user wear protective clothing, gloves, and eye/face protection in order to avoid contact with skin and eyes.
- 50 µg/ml
- Storage & Handling
- Protect from light. Store between 2°C and 8°C.
FC - Quality tested
- Recommended Usage
For dead cell exclusion, resuspend cell pellet in 0.5 mL of Cell Staining Buffer and add 5 µl of 7-AAD per million cells and incubate for 5-10 minutes in the dark before analysis. The analysis of the cells should be done as soon as possible after the incubation with the dye.
We recommend utilizing our Fluorescence Spectra Analyzer to determine compatibility of 7AAD with other fluorochromes.
- Excitation Laser
Blue Laser (488 nm)
- Application Notes
7-AAD Viability Staining Solution can be used as a viability probe for methods of nonviable cell exclusion.
- Additional Product Notes
View more applications data for this product in our Scientific Poster Library.
(PubMed link indicates BioLegend citation)
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- Jaworska J, et al. 2015. J Immunol. 194:325. PubMed
- Product Citations
- Biology Area
- Cell Biology, Cell Cycle/DNA Replication, Cell Proliferation and Viability, Neuroscience
- Antigen References
1. Schmid I, et al. 1992. Cytometry. 13:204
- Gene ID
- Why is washing not recommended after the addition 7-AAD or PI addition when assessing viability?
These dyes bind in equilibrium with DNA. Therefore, external dye concentration must be maintained during analysis and the dye should not be washed out.