No discussions found
Start your discussion
Share your thoughts or question with experts in your field
Start a discussion
Found 4 matching solutions for this experiment
Upstream tips |
Protocol tips |
Downstream tips |
- Cells were pretreated with Sal A for 4 h and then washed before adding 10 µM ATO and incubating for 24 h |
- Cells were resuspended in 400 mL of the 25 mM carboxy-H2DCFDA working solution, incubated in the dark for 20–30 min at 37 °C, |
|
Upstream tips |
- Cells were pretreated with Sal A for 4 h and then washed before adding 10 µM ATO and incubating for 24 h |
Protocol tips |
- Cells were resuspended in 400 mL of the 25 mM carboxy-H2DCFDA working solution, incubated in the dark for 20–30 min at 37 °C, |
Upstream tips |
Protocol tips |
Downstream tips |
|
- Cells were treated with DCFDA.
- After diffusion into the cells, DCFDA was deacetylated by cellular esterases to a non-fluorescent compound, which was later oxidized by ROS into 2′,7′-dichlorofluorescin (DCF) |
|
Protocol tips |
- Cells were treated with DCFDA.
- After diffusion into the cells, DCFDA was deacetylated by cellular esterases to a non-fluorescent compound, which was later oxidized by ROS into 2′,7′-dichlorofluorescin (DCF) |
Upstream tips |
Protocol tips |
Downstream tips |
- 50,000 cells/well were seeded |
- Cells werre treated with α-TOS, NTα-TOS-NPs, or T-α-TOS-NPs for 12 h at 37 °C in 5% CO2.
- RIPA cell lysis buffer was
added and mixed for 2 min |
|
Upstream tips |
- 50,000 cells/well were seeded |
Protocol tips |
- Cells werre treated with α-TOS, NTα-TOS-NPs, or T-α-TOS-NPs for 12 h at 37 °C in 5% CO2.
- RIPA cell lysis buffer was
added and mixed for 2 min |
Upstream tips |
Protocol tips |
Downstream tips |
|
- Cells were treated with Superoxide Detection Solution and then incubated for 30 min |
|
Protocol tips |
- Cells were treated with Superoxide Detection Solution and then incubated for 30 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!