No discussions found
Start your discussion
Share your thoughts or question with experts in your field
Start a discussion
Found 2 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
|
Fix cells with 0.5 mL 1Х fixative solution for 15 min at room temperature.
Add 1 ml of the β-Galactosidase Staining Solution and incubate the plate at 37°C at least overnight in a dry incubator (no CO2) |
Visualise cells after 11 to 14 hr, |
Protocol tips |
Fix cells with 0.5 mL 1Х fixative solution for 15 min at room temperature.
Add 1 ml of the β-Galactosidase Staining Solution and incubate the plate at 37°C at least overnight in a dry incubator (no CO2) |
Downstream tips |
Visualise cells after 11 to 14 hr, |
Upstream tips |
Protocol tips |
Downstream tips |
Warm enough Reaction Buffer and Reaction Substrate for the entire experiment to room temperature |
Add 200 µl of the Reaction Buffer Mixture to each cell lysate and mix gently.
Incubate at room temperature (20–25°C) for 60 min |
|
Upstream tips |
Warm enough Reaction Buffer and Reaction Substrate for the entire experiment to room temperature |
Protocol tips |
Add 200 µl of the Reaction Buffer Mixture to each cell lysate and mix gently.
Incubate at room temperature (20–25°C) for 60 min |
Can't find the product you've used to perform this experiment? It would be great if you can help us by
Adding a product!