Seed cells on 96-well plates by 5000 cells/well and treat with oridonin, with, as indicated, final concentrations for a different duration. Fix cells in situ with 40% (w/v) cold Trichloroacetic acid (TCA). Let them sit for 5 min. Incubate plates at 4 °C for 1 h. Discard supernatant and gently wash plates 5 times with water, followed by an air-dry. Stain fixed cells with 0.4% (w/v) SRB with 1% acetic acid as solubilizer. After staining, wash with 1% acetic acid to remove the free dye and air-dry. Solubilize the bound stain with 100 mM Tris Base for reading. Read absorbance on a microplate reader at 515 nm [45 (link),46 (link)]. Inhibition% = [(OD control − OD treated)]/OD control] × 100%.
Oridonin Compound Cytotoxicity Assay
Seed cells on 96-well plates by 5000 cells/well and treat with oridonin, with, as indicated, final concentrations for a different duration. Fix cells in situ with 40% (w/v) cold Trichloroacetic acid (TCA). Let them sit for 5 min. Incubate plates at 4 °C for 1 h. Discard supernatant and gently wash plates 5 times with water, followed by an air-dry. Stain fixed cells with 0.4% (w/v) SRB with 1% acetic acid as solubilizer. After staining, wash with 1% acetic acid to remove the free dye and air-dry. Solubilize the bound stain with 100 mM Tris Base for reading. Read absorbance on a microplate reader at 515 nm [45 (link),46 (link)]. Inhibition% = [(OD control − OD treated)]/OD control] × 100%.
Corresponding Organization : Zhengzhou University
Variable analysis
- Oridonin concentration
- Oridonin treatment duration
- Cell viability/proliferation as measured by SRB assay
- Cell seeding density (5000 cells/well)
- Cell culture medium (DMSO for oridonin, PBS for gemcitabine)
- Incubation conditions (4°C for 1 hour after TCA fixation)
- Positive control: Not explicitly mentioned
- Negative control: Not explicitly mentioned
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