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71 cell f-software  (Evident Corporation)

 
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    Evident Corporation 71 cell f-software
    Morphologic profiling of Sulfasalazine, DHA and the novel hybrid compound AC254 on rodent glioma cells. ( A ) Rat glioma cells (F98) were treated with a range of concentrations of SAS, DHA, AC254, SAS and solvent DMSO combined with DHA. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with <t>cell</t> <t>F-Software</t> (Olympus). Scale bar, 200 µM. ( B ) F98 were treated with 0.5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bar: 20 µm.
    71 Cell F Software, supplied by Evident Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/71+cell+f-software/NoviSight+3D+Cell+Analysis+Software/pmc08531376-243-4-6
    Average 90 stars, based on 1 article reviews
    71 cell f-software - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death"

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death

    Journal: Scientific Reports

    doi: 10.1038/s41598-021-99960-z

    Morphologic profiling of Sulfasalazine, DHA and the novel hybrid compound AC254 on rodent glioma cells. ( A ) Rat glioma cells (F98) were treated with a range of concentrations of SAS, DHA, AC254, SAS and solvent DMSO combined with DHA. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µM. ( B ) F98 were treated with 0.5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bar: 20 µm.
    Figure Legend Snippet: Morphologic profiling of Sulfasalazine, DHA and the novel hybrid compound AC254 on rodent glioma cells. ( A ) Rat glioma cells (F98) were treated with a range of concentrations of SAS, DHA, AC254, SAS and solvent DMSO combined with DHA. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µM. ( B ) F98 were treated with 0.5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bar: 20 µm.

    Techniques Used: Light Microscopy, Software, Staining, Marker

    Effects on human cell viability (U87, TN22). ( A ) Cells (U87) were treated with 1 µM of the compounds. Cell viability was measured after 72 h. n = 4. * indicates significance to control ( p < 0.05). ( B ) U87 were treated with various concentrations of the compounds. Cell viability was measured the same way as in A. n = 4. * indicates significance to control ( p < 0.05). ( C ) TN22 were treated with 5 µM of the compounds. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µm. ( D ) TN22 were treated with 5 µM of the compounds, cell viability was measured after 72 h. n = 4. * indicates significance to control ( p < 0.05).
    Figure Legend Snippet: Effects on human cell viability (U87, TN22). ( A ) Cells (U87) were treated with 1 µM of the compounds. Cell viability was measured after 72 h. n = 4. * indicates significance to control ( p < 0.05). ( B ) U87 were treated with various concentrations of the compounds. Cell viability was measured the same way as in A. n = 4. * indicates significance to control ( p < 0.05). ( C ) TN22 were treated with 5 µM of the compounds. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µm. ( D ) TN22 were treated with 5 µM of the compounds, cell viability was measured after 72 h. n = 4. * indicates significance to control ( p < 0.05).

    Techniques Used: Light Microscopy, Software

    Impact on human cell morphology. ( A ) Human cells (U87) were treated with a variation of concentrations of SAS, DHA, their covalently bound hybrid (AC254) and their 1:1 mixture. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µM. ( B ) Cells (U87) were treated with 5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bars represents 20 µm.
    Figure Legend Snippet: Impact on human cell morphology. ( A ) Human cells (U87) were treated with a variation of concentrations of SAS, DHA, their covalently bound hybrid (AC254) and their 1:1 mixture. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µM. ( B ) Cells (U87) were treated with 5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bars represents 20 µm.

    Techniques Used: Light Microscopy, Software, Staining, Marker

    Impact of the compounds on cell migration. ( A , B , C ) A scratch was made into plated cells (F98) after 36 h. Cells were then treated with 0.5 µM ( A ) and 5 µM ( B , C ) of the compounds. Representative images were taken (Olympus × 71 with cell F-Software (Olympus)). ( B ), quantified and related to the time the scratch was made (0 h) ( A , C ). n = 3. * indicates significance to control ( p < 0.05).
    Figure Legend Snippet: Impact of the compounds on cell migration. ( A , B , C ) A scratch was made into plated cells (F98) after 36 h. Cells were then treated with 0.5 µM ( A ) and 5 µM ( B , C ) of the compounds. Representative images were taken (Olympus × 71 with cell F-Software (Olympus)). ( B ), quantified and related to the time the scratch was made (0 h) ( A , C ). n = 3. * indicates significance to control ( p < 0.05).

    Techniques Used: Migration, Software

    Related Articles

    Light Microscopy:

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death
    Article Snippet: Olympus × 71 with cell F-Software (Olympus).

    Software:

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death
    Article Snippet: Olympus × 71 with cell F-Software (Olympus).

    Staining:

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death
    Article Snippet: Olympus × 71 with cell F-Software (Olympus).

    Marker:

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death
    Article Snippet: Olympus × 71 with cell F-Software (Olympus).

    Migration:

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death
    Article Snippet: Olympus × 71 with cell F-Software (Olympus).



    Similar Products

    71 cell f-software  (Evident Corporation)
    90
    Evident Corporation 71 cell f-software
    Morphologic profiling of Sulfasalazine, DHA and the novel hybrid compound AC254 on rodent glioma cells. ( A ) Rat glioma cells (F98) were treated with a range of concentrations of SAS, DHA, AC254, SAS and solvent DMSO combined with DHA. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with <t>cell</t> <t>F-Software</t> (Olympus). Scale bar, 200 µM. ( B ) F98 were treated with 0.5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bar: 20 µm.
    71 Cell F Software, supplied by Evident Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/71+cell+f-software/NoviSight+3D+Cell+Analysis+Software/pmc08531376-243-4-6
    Average 90 stars, based on 1 article reviews
    71 cell f-software - by Bioz Stars, 2026-10
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Morphologic profiling of Sulfasalazine, DHA and the novel hybrid compound AC254 on rodent glioma cells. ( A ) Rat glioma cells (F98) were treated with a range of concentrations of SAS, DHA, AC254, SAS and solvent DMSO combined with DHA. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µM. ( B ) F98 were treated with 0.5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bar: 20 µm.

    Journal: Scientific Reports

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death

    doi: 10.1038/s41598-021-99960-z

    Figure Lengend Snippet: Morphologic profiling of Sulfasalazine, DHA and the novel hybrid compound AC254 on rodent glioma cells. ( A ) Rat glioma cells (F98) were treated with a range of concentrations of SAS, DHA, AC254, SAS and solvent DMSO combined with DHA. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µM. ( B ) F98 were treated with 0.5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bar: 20 µm.

    Article Snippet: Olympus × 71 with cell F-Software (Olympus).

    Techniques: Light Microscopy, Software, Staining, Marker

    Effects on human cell viability (U87, TN22). ( A ) Cells (U87) were treated with 1 µM of the compounds. Cell viability was measured after 72 h. n = 4. * indicates significance to control ( p < 0.05). ( B ) U87 were treated with various concentrations of the compounds. Cell viability was measured the same way as in A. n = 4. * indicates significance to control ( p < 0.05). ( C ) TN22 were treated with 5 µM of the compounds. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µm. ( D ) TN22 were treated with 5 µM of the compounds, cell viability was measured after 72 h. n = 4. * indicates significance to control ( p < 0.05).

    Journal: Scientific Reports

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death

    doi: 10.1038/s41598-021-99960-z

    Figure Lengend Snippet: Effects on human cell viability (U87, TN22). ( A ) Cells (U87) were treated with 1 µM of the compounds. Cell viability was measured after 72 h. n = 4. * indicates significance to control ( p < 0.05). ( B ) U87 were treated with various concentrations of the compounds. Cell viability was measured the same way as in A. n = 4. * indicates significance to control ( p < 0.05). ( C ) TN22 were treated with 5 µM of the compounds. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µm. ( D ) TN22 were treated with 5 µM of the compounds, cell viability was measured after 72 h. n = 4. * indicates significance to control ( p < 0.05).

    Article Snippet: Olympus × 71 with cell F-Software (Olympus).

    Techniques: Light Microscopy, Software

    Impact on human cell morphology. ( A ) Human cells (U87) were treated with a variation of concentrations of SAS, DHA, their covalently bound hybrid (AC254) and their 1:1 mixture. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µM. ( B ) Cells (U87) were treated with 5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bars represents 20 µm.

    Journal: Scientific Reports

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death

    doi: 10.1038/s41598-021-99960-z

    Figure Lengend Snippet: Impact on human cell morphology. ( A ) Human cells (U87) were treated with a variation of concentrations of SAS, DHA, their covalently bound hybrid (AC254) and their 1:1 mixture. Cell morphology was examined after 72 h with light microscopy. Olympus × 71 with cell F-Software (Olympus). Scale bar, 200 µM. ( B ) Cells (U87) were treated with 5 µM of SAS, DHA, AC254 and SAS combined with. Cells were fixated and stained with actin marker Phalloidin 488 and DNA marker Hoechst after 24 h of treatment. Axio Observer with Zen Software (Zeiss). Scale bars represents 20 µm.

    Article Snippet: Olympus × 71 with cell F-Software (Olympus).

    Techniques: Light Microscopy, Software, Staining, Marker

    Impact of the compounds on cell migration. ( A , B , C ) A scratch was made into plated cells (F98) after 36 h. Cells were then treated with 0.5 µM ( A ) and 5 µM ( B , C ) of the compounds. Representative images were taken (Olympus × 71 with cell F-Software (Olympus)). ( B ), quantified and related to the time the scratch was made (0 h) ( A , C ). n = 3. * indicates significance to control ( p < 0.05).

    Journal: Scientific Reports

    Article Title: Chemical hybridization of sulfasalazine and dihydroartemisinin promotes brain tumor cell death

    doi: 10.1038/s41598-021-99960-z

    Figure Lengend Snippet: Impact of the compounds on cell migration. ( A , B , C ) A scratch was made into plated cells (F98) after 36 h. Cells were then treated with 0.5 µM ( A ) and 5 µM ( B , C ) of the compounds. Representative images were taken (Olympus × 71 with cell F-Software (Olympus)). ( B ), quantified and related to the time the scratch was made (0 h) ( A , C ). n = 3. * indicates significance to control ( p < 0.05).

    Article Snippet: Olympus × 71 with cell F-Software (Olympus).

    Techniques: Migration, Software