X-Gal staining of Mouse Embrional Stem cells grown on the cellular matrix

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FuGENE®HD


Reagent / DNA Ratio
0.25μl/0.1μg
5μl Complex per well
Complex Incubation 15 min

Lipofectamine® 2000


Reagent / DNA Ratio
0.5μl/0.2μg
50μl Complex per well
Complex Incubation 20 min

FuGENE™6


Reagent / DNA Ratio
0.6μl/0.1μg
10μl Complex per well
Complex Incubation 15 min
Transfection with competitor reagent was performed according to manufacturer’s instructions

Protocol for Mouse ES Cell Transfection by FuGENE HD

  1. Cell plating

    Mouse ES cells (from Celprogen Inc.) were seeded the day before transfection with the density 10,000 cells per well in 100 μl Mouse Embryonic Stem Cell Expansion (Celprogen Inc) complete growth medium.

  2. Complex preparation (per 20 wells)

    Tissue culture 96-round bottom well plates were used for complex preparation:

    1. Prepare 0.02μg/μl pCMVβ DNA solution in OptiMEM®.
    2. Add 5 μl of reagent to 100 μl of OptiMEM® /DNA solution.
    3. Mix carefully by pipetting (10-15 times).
    4. Incubate 15 min at room temperature.
    5. Add 5μl complex per well to the cells, and mix thoroughly.
  3. Incubation

    Place the cells into CO2 incubator for 24 hours.

  4. Detection of β-gal expression
    1. Remove the medium from the well and wash the cells once with 100μl per well PBS.
    2. Fix the cells in the well with 50μl solution of 4% formaldehyde in PBS for 5min at room temperature.
    3. Wash each well twice with 100μl PBS.
    4. Add 50μl per well of substrate/stain solution and incubate the plate overnight at 37°C.
    5. Observe the cells under microscope and evaluate the proportion of blue (β-gal-positive) cells.