Store in the dark at 2-8°C. Avoid prolonged exposure to light. Do not freeze!
规格:
100T
Figure 1: Flow Cytometry - Annexin V (Dyomics 647) (A285885) Separation of Annexin positive Hoechst 34580 positive events (red-filled) from Annexin negative Hoechst 34580 negative events (black-dashed) in flow cytometry analysis (surface staining) of camptothecin induced apoptotic Jurkat cells stained using Annexin V (Dyomics 647) (5 µl reagent per million cells in 100 µl of cell suspension).
Figure 2: Flow Cytometry - Annexin V (Dyomics 647) (A285885) Flow cytometry multicolor surface staining of camptothecin induced apoptotic Jurkat cells stained using Annexin V (Dyomics 647) (5 µl reagent per million cells in 100 µl of cell suspension) and Hoechst 34580 viability stain.
Figure 3: Flow Cytometry - Annexin V (Dyomics 647) (A285885) Flow cytometry multicolor surface staining of camptothecin induced apoptotic Jurkat cells stained using Annexin V (Dyomics 647) (5 µl reagent per million cells in 100 µl of cell suspension) and Propidium Iodide (5 µl reagent per million cells in 100 µl of cell suspension).
Figure 4: Flow Cytometry - Annexin V (Dyomics 647) (A285885) Separation of Annexin stained apoptotic Jurkat cells (red-filled) from unstained cells (black-dashed) in flow cytometry analysis (surface staining) of camptothecin induced apoptotic Jurkat cells stained using Annexin V (Dyomics 647) (5 µl reagent per million cells in 100 µl of cell suspension).
Figure 5: Flow Cytometry - Annexin V (Dyomics 647) (A285885) Flow cytometry surface staining pattern of camptothecin induced apoptotic Jurkat cells stained using Annexin V (Dyomics 647) (5 µl reagent per million cells in 100 µl of cell suspension).