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 |
- cells were seeded at 5×104 cells/ml and treated with IC50 values of AFha, AFe and Cha and incubated for 16 and 32 h |
- 100 µl lysis reagent were added to each tube and incubated for 5 min at room temperature. |
|
Upstream tips |
- cells were seeded at 5×104 cells/ml and treated with IC50 values of AFha, AFe and Cha and incubated for 16 and 32 h |
Protocol tips |
- 100 µl lysis reagent were added to each tube and incubated for 5 min at room temperature. |
Upstream tips |
Protocol tips |
Downstream tips |
|
- Cells are labelled with EdU for 20min |
- For the detection of EdU with Alexa Fluor® 647 azide use 633/635 nm excitation with a red emission filter (660/20 nm or similar). |
Protocol tips |
- Cells are labelled with EdU for 20min |
Downstream tips |
- For the detection of EdU with Alexa Fluor® 647 azide use 633/635 nm excitation with a red emission filter (660/20 nm or similar). |
Upstream tips |
Protocol tips |
Downstream tips |
|
- Cells are incubated with securinine at concentrations of 10.0 and 20.0 μg/ml for 24 h and 48 h. DMSO concentration added to the cells was 0.2% (v/v) |
|
Protocol tips |
- Cells are incubated with securinine at concentrations of 10.0 and 20.0 μg/ml for 24 h and 48 h. DMSO concentration added to the cells was 0.2% (v/v) |
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!