NUCLEAR-ID^® Blue/Green cell viability reagent

Manuals And Inserts

• Datasheet

Specific Protocol

Wide Field Fluorescence/Confocal Microscopy
Reagent Preparation:
Mix 1μL of NUCLEAR-ID^® Blue/Green Cell Viability Reagent in 1 mL of buffer of choice. This volume is sufficient for 10 assays and may be scaled according to need.

Staining Adherent cells:

1. Grow cells directly onto glass slides or polystyrene tissue culture plates until ~80% confluent via standard tissue culture practices.
2. Remove growth media.
3. Dispense the freshly diluted staining solution in a volume sufficient for covering the cell monolayer.

<li<Protect samples from light and incubate for 30 minutes at 37°C.

4. Remove the excess staining solution and, if necessary, add a few drops of buffer to prevent the cells from drying out.
5. Cover cells with a glass cover slip and observe under a fluorescence/confocal microscope with a dual filter set for DAPI (Ex/Em: 350/470nm) and GFP/FITC (Ex/Em: 488/514 nm).

Staining Non-Adherent Cells:

Grow cells via standard tissue culture practices. 

1. Collect about 1 x 10⁵ cells. Centrifuge at 500 x g for 5 minutes. Remove supernatant.
2. Re-suspend cells in a volume of the freshly diluted staining solution sufficient for covering the cell pellet.
3. Protect samples from light and incubate for 30 minutes at 37°C.
4. Centrifuge at 500 x g for 5 minutes. Remove supernatant.
5. Re-suspend cells in 100µL buffer
6. Plate 10-15µL of cells on a glass slide.
7. 8. Cover cells with a glass cover slip and observe under a fluorescence/confocal microscope with a dual filter set for DAPI (Ex/Em: 350/470nm)and GFP/FITC (Ex/Em: 488/514 nm).

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