No discussions found
Start your discussion
Share your thoughts or question with experts in your field
Start a discussion
Found 3 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
Seed cells fro 72 hours and washe twice with PBS,
Fix for 6 min with fixation buffer containing 2% formaldehyde, 0.2% glutaraldehyde, 7.0 mM Na2HPO4, 1.5 mM KH2PO4, 140 mM NaCl, and 2.68 mM KCl |
Add 1 ml of the Staining Mixture per well and incubate overnight at 37 °C without CO2 until the cells are stained blue. |
|
Upstream tips |
Seed cells fro 72 hours and washe twice with PBS,
Fix for 6 min with fixation buffer containing 2% formaldehyde, 0.2% glutaraldehyde, 7.0 mM Na2HPO4, 1.5 mM KH2PO4, 140 mM NaCl, and 2.68 mM KCl |
Protocol tips |
Add 1 ml of the Staining Mixture per well and incubate overnight at 37 °C without CO2 until the cells are stained blue. |
Upstream tips |
Protocol tips |
Downstream tips |
|
Fix the cells with 0.5 ml of Fixative Solution for 10 - 15 min at room temperature
Add 0.5 ml of the Staining Solution Mix to each well. Cover the plate. Incubate overnight at 37°C. |
|
Protocol tips |
Fix the cells with 0.5 ml of Fixative Solution for 10 - 15 min at room temperature
Add 0.5 ml of the Staining Solution Mix to each well. Cover the plate. Incubate overnight at 37°C. |
Upstream tips |
Protocol tips |
Downstream tips |
Seed 5 × 10^4 cells |
Add 100µL of β-Galactosidase Assay Reagent.
Cover plate and incubate for 30 minutes at 37°C. |
Measure absorbance at 405nm. |
Upstream tips |
Seed 5 × 10^4 cells |
Protocol tips |
Add 100µL of β-Galactosidase Assay Reagent.
Cover plate and incubate for 30 minutes at 37°C. |
Downstream tips |
Measure absorbance at 405nm. |
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!