Calculator
CytoTell™ Green
Flow cytometry combined with fluorescence staining is a powerful tool to analyze heterogeneous cell populations. Among all the existing fluorescent dyes CFSE is the preferred cell proliferation indicator that is widely used for live cell analysis. However, there are a few severe problems associated with the use of CFSE for monitoring cell proliferation. 1). CFSE is highly toxic to cells. CFSE indiscriminately reacts with all amino groups, thus changes many critical intracellular protein functions (such as cell membrane GPCRs); 2). CFSE has slow response and is inconvenient to use. The CFSE fluorescence intensity of the 2nd generation cells is decreased more than 10 fold from the 1st generation. You would have to wait for another generation to start the cell proliferation analysis. 3). Medium removal is required. You would have to remove medium for cell analysis with a flow cytometer since CFSE reacts with medium components. CytoTell™ Green is developed to eliminate these limitations. It has distinct advantages over CFSE. 1). CytoTell™ Green has very minimal cytotoxicity compared to CFSE. It is well retained in cells since the probe is designed to minimize the MDR interaction that generally pumps many cell stains out cells; 2). CytoTell™ Green exhibits much faster response and is more convenient to use than CFSE. There is no fluorescence intensity gap between 1st and 2nd generation of cells. As cells divide, CytoTell™ Green is distributed equally between daughter cells that can be measured as successive halving of the fluorescence intensity of the dye; 3). There is no need to remove medium since CytoTell™ Green does not react with medium components; 4). CytoTell™ Green is more sensitive than CFSE. Up to 9 generations may be visualized; 5). CytoTell™ Green is much more stable than CFSE. CytoTell™ Green stock solution can be stored at room temperature for a few days. CytoTell™ Green can also be used for long term tracking of labeled cells. Analysis using two-parameter plots may provide better resolution of each generation, especially between undivided cells and the first generation. Cells labeled with CytoTell™ Green may be fixed and permeabilized for analysis of intracellular targets using standard formaldehyde-containing fixatives and saponin-based permeabilization buffers. CytoTell™ Green has a peak excitation of 510 nm and can be excited by the blue (488 nm) laser line, making it compatible with FITC filter set.
Example protocol
AT A GLANCE
Protocol Summary
- Prepare cells with test compounds
- Add 1X dye working solution
- Incubate dyes with cells at room temperature or 37 oC for 10 to 30 minutes
- Remove the dye working solution
- Analyse with flow cytometer with appropriate filter set
Important Note
Bring all the kit components to room temperature before starting the experiment.
Note: The CytoTell™ dyes are lyophilized powders. They should be stable for at least 6 months if stored at -20 °C, protecting from light and avoiding freeze/thaw cycles.
PREPARATION OF STOCK SOLUTIONS
Unless otherwise noted, all unused stock solutions should be divided into single-use aliquots and stored at -20 °C after preparation. Avoid repeated freeze-thaw cycles
CytoTell™ dye stock solution (500X)
Add 500 µL DMSO into the dye powder vial, and mix it well by vortexing to have a stock solution (500X).
Note: The stock solution should be used promptly. Any remaining solution should be aliquoted and frozen at < - 20 oC. Avoid repeated freeze-thaw cycles, and protect from light.
PREPARATION OF WORKING SOLUTION
CytoTell™ dye working solution (1X)
Dilute the 500X DMSO stock solution at 1 to 500 in Hanks and 20 mM Hepes buffer (HHBS) or the buffer of your choice, pH 7 (such as 1 µL of 500X DMSO stock solution to 500 µL buffer) right before use. Mix them well by vortexing.
Note: The final concentration of the dye working solution should be empirically determined for different cell types and/or experimental conditions. It is recommended to test at the concentrations that are at least over tenfold range. Such as, CytoTell™ Red might use much less amount in some cell types than the recommended concentrations.
SAMPLE EXPERIMENTAL PROTOCOL
- Treat cells with test compounds for a desired period of time.
- Centrifuge the cells to get 1-5 × 105 cells per tube.
- Resuspend cells in 500 µL of the CytoTell™ dye working solution. Optional: One can add the 500X DMSO stock solution into the cells directly without medium removing (such as, add 1 µL500X DMSO stock solution into 500 µL cells)
- Incubate cells with a dye solution at room temperature or 37 °C for 10 to 30 minutes, protected from light.
- Remove the dye working solution from the cells, wash the cells with HHBS or buffer of your choice. Resuspend cells in 500 µL of pre-warmed HHBS or medium to get 1-5 × 105 cells per tube.
Monitor the fluorescence change at respected Ex/Em (see Key Parameters) with a flow cytometer or a fluorescence microscope.
Calculators
Common stock solution preparation
Table 1. Volume of DMSO needed to reconstitute specific mass of CytoTell™ Green to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.
| 0.1 mg | 0.5 mg | 1 mg | 5 mg | 10 mg | |
| 1 mM | 238.527 µL | 1.193 mL | 2.385 mL | 11.926 mL | 23.853 mL |
| 5 mM | 47.705 µL | 238.527 µL | 477.054 µL | 2.385 mL | 4.771 mL |
| 10 mM | 23.853 µL | 119.263 µL | 238.527 µL | 1.193 mL | 2.385 mL |
Molarity calculator
Enter any two values (mass, volume, concentration) to calculate the third.
| Mass (Calculate) | Molecular weight | Volume (Calculate) | Concentration (Calculate) | Moles | ||||
| / | = | x | = |
Spectrum
Product family
| Name | Excitation (nm) | Emission (nm) |
| CytoTell™ Blue | 410 | 445 |
| CytoTell™ Orange | 541 | 560 |
Citations
View all 26 citations: Citation Explorer
The CH1 domain influences the expression and antigen sensing of the HIV-specific CH31 IgM-BCR and IgG-BCR
Authors: Ortiz, Yaneth and Anasti, Kara and Pane, Advaiti K and Cronin, Kenneth and Alam, S Munir and Reth, Michael
Journal: Proceedings of the National Academy of Sciences (2024): e2404728121
Authors: Ortiz, Yaneth and Anasti, Kara and Pane, Advaiti K and Cronin, Kenneth and Alam, S Munir and Reth, Michael
Journal: Proceedings of the National Academy of Sciences (2024): e2404728121
A co-culture system of macrophages with breast cancer tumoroids to study cell interactions and therapeutic responses
Authors: Raffo-Romero, Antonella and Ziane-Chaouche, Lydia and Salom{\'e}-Desnoulez, Sophie and Hajjaji, Nawale and Fournier, Isabelle and Salzet, Michel and Duhamel, Marie
Journal: Cell Reports Methods (2024)
Authors: Raffo-Romero, Antonella and Ziane-Chaouche, Lydia and Salom{\'e}-Desnoulez, Sophie and Hajjaji, Nawale and Fournier, Isabelle and Salzet, Michel and Duhamel, Marie
Journal: Cell Reports Methods (2024)
Optimizing lentiviral vector formulation conditions for efficient ex vivo transduction of primary human T cells in chimeric antigen receptor T-cell manufacturing
Authors: Luostarinen, Annu and Kailaanm{\"a}ki, Anssi and Turkki, Vesa and K{\"o}ylij{\"a}rvi, Marjut and K{\"a}yhty, Piia and Leinonen, Hanna and Albers-Skirdenko, Vita and Lipponen, Eevi and Yl{\"a}-Herttuala, Seppo and Kaartinen, Tanja and others,
Journal: Cytotherapy (2024)
Authors: Luostarinen, Annu and Kailaanm{\"a}ki, Anssi and Turkki, Vesa and K{\"o}ylij{\"a}rvi, Marjut and K{\"a}yhty, Piia and Leinonen, Hanna and Albers-Skirdenko, Vita and Lipponen, Eevi and Yl{\"a}-Herttuala, Seppo and Kaartinen, Tanja and others,
Journal: Cytotherapy (2024)
Effective targeting of breast cancer by the inhibition of P-glycoprotein mediated removal of toxic lipid peroxidation byproducts from drug tolerant persister cells
Authors: Szeb{\'e}nyi, Korn{\'e}lia and F{\"u}redi, Andr{\'a}s and Bajtai, Eszter and Sama, Sai Nagender and Csiszar, Agnes and Gombos, Bal{\'a}zs and Szab{\'o}, P{\'a}l and Grusch, Michael and Szak{\'a}cs, Gergely
Journal: Drug Resistance Updates (2023): 101007
Authors: Szeb{\'e}nyi, Korn{\'e}lia and F{\"u}redi, Andr{\'a}s and Bajtai, Eszter and Sama, Sai Nagender and Csiszar, Agnes and Gombos, Bal{\'a}zs and Szab{\'o}, P{\'a}l and Grusch, Michael and Szak{\'a}cs, Gergely
Journal: Drug Resistance Updates (2023): 101007
Concurrent stimulation of monocytes with CSF1 and polarizing cytokines reveals phenotypic and functional differences with classical polarized macrophages
Authors: An, Liying and Michaeli, Julia and Pallavi, Prama and Breedijk, Annette and Xu, Xin and Dietrich, Nadine and Sigl, Martin and Keese, Michael and Nitschke, Katja and Jarczyk, Jonas and others,
Journal: Journal of Leukocyte Biology (2022)
Authors: An, Liying and Michaeli, Julia and Pallavi, Prama and Breedijk, Annette and Xu, Xin and Dietrich, Nadine and Sigl, Martin and Keese, Michael and Nitschke, Katja and Jarczyk, Jonas and others,
Journal: Journal of Leukocyte Biology (2022)
Page updated on November 21, 2024
Safety data sheet