sir-dna dye Search Results


dna vital dye sir hoechst  (Spirochrome)
97
Spirochrome dna vital dye sir hoechst
Dna Vital Dye Sir Hoechst, supplied by Spirochrome, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sir-dna+dye/SiR-DNA/pmc06781431-111-0-4
Average 97 stars, based on 1 article reviews
dna vital dye sir hoechst - by Bioz Stars, 2026-10
97/100 stars
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sir dna dye  (Cytoskeleton Inc)
96
Cytoskeleton Inc sir dna dye
A Western blots were performed on mitotic lysates generated from the panel of cell lines depleted of ZNF768 with inducible sh_ZNF768_1 ( n =3). B Representative immunofluorescence image of mitotic inducible HeLa cells after 48 hours doxycycline induction. Cells were stained for PLK1 (green), CENPC (grey) and with Hoechst (blue). C Quantification of the average relative intensity of PLK1 at kinetochores from ( B ) using previous inducible cancer cell lines ( n =3). D Representative stills of time-lapse movies of inducible HeLa cells after a 48 hours ZNF768 knockdown. For imaging, cells were synchronized in mitosis after release from a double thymidine block and incubated <t>with</t> <t>SiR-DNA</t> to visualize the chromatin. E Quantification of the average nuclear envelope breakdown to the anaphase onset duration in the indicated cell lines ( n = n=3 for all cell lines except for the HeLa, n=4). F Representative live cell images of mitotic defects observed after 48 hour ZNF768 depletion in HeLa cells. G Quantification of mitotic defects listed in F in MDA-MB-231, HeLa, HCT-116 and U87 cell lines after 48 hour ZNF768 depletion ( n =3). In all panels, data represent the mean ± SEM. In panel C , E and G , significance was determined by unpaired t test.
Sir Dna Dye, supplied by Cytoskeleton Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sir-dna+dye/SiR-DNA+Kit/bio_rxiv__64898__2026__08__03__742597-302-11-14
Average 96 stars, based on 1 article reviews
sir dna dye - by Bioz Stars, 2026-10
96/100 stars
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lf635/lp-b-000  (IDEX)
90
IDEX lf635/lp-b-000
A Western blots were performed on mitotic lysates generated from the panel of cell lines depleted of ZNF768 with inducible sh_ZNF768_1 ( n =3). B Representative immunofluorescence image of mitotic inducible HeLa cells after 48 hours doxycycline induction. Cells were stained for PLK1 (green), CENPC (grey) and with Hoechst (blue). C Quantification of the average relative intensity of PLK1 at kinetochores from ( B ) using previous inducible cancer cell lines ( n =3). D Representative stills of time-lapse movies of inducible HeLa cells after a 48 hours ZNF768 knockdown. For imaging, cells were synchronized in mitosis after release from a double thymidine block and incubated <t>with</t> <t>SiR-DNA</t> to visualize the chromatin. E Quantification of the average nuclear envelope breakdown to the anaphase onset duration in the indicated cell lines ( n = n=3 for all cell lines except for the HeLa, n=4). F Representative live cell images of mitotic defects observed after 48 hour ZNF768 depletion in HeLa cells. G Quantification of mitotic defects listed in F in MDA-MB-231, HeLa, HCT-116 and U87 cell lines after 48 hour ZNF768 depletion ( n =3). In all panels, data represent the mean ± SEM. In panel C , E and G , significance was determined by unpaired t test.
Lf635/Lp B 000, supplied by IDEX, 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/sir-dna+dye/alexa+fluor+647/pmc11701221-93-23-23
Average 90 stars, based on 1 article reviews
lf635/lp-b-000 - by Bioz Stars, 2026-10
90/100 stars
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sir dna dye spirochrome  (Thermo Fisher)
99
Thermo Fisher sir dna dye spirochrome
A Western blots were performed on mitotic lysates generated from the panel of cell lines depleted of ZNF768 with inducible sh_ZNF768_1 ( n =3). B Representative immunofluorescence image of mitotic inducible HeLa cells after 48 hours doxycycline induction. Cells were stained for PLK1 (green), CENPC (grey) and with Hoechst (blue). C Quantification of the average relative intensity of PLK1 at kinetochores from ( B ) using previous inducible cancer cell lines ( n =3). D Representative stills of time-lapse movies of inducible HeLa cells after a 48 hours ZNF768 knockdown. For imaging, cells were synchronized in mitosis after release from a double thymidine block and incubated <t>with</t> <t>SiR-DNA</t> to visualize the chromatin. E Quantification of the average nuclear envelope breakdown to the anaphase onset duration in the indicated cell lines ( n = n=3 for all cell lines except for the HeLa, n=4). F Representative live cell images of mitotic defects observed after 48 hour ZNF768 depletion in HeLa cells. G Quantification of mitotic defects listed in F in MDA-MB-231, HeLa, HCT-116 and U87 cell lines after 48 hour ZNF768 depletion ( n =3). In all panels, data represent the mean ± SEM. In panel C , E and G , significance was determined by unpaired t test.
Sir Dna Dye Spirochrome, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sir-dna+dye/DNA/pm31677225-200-37-62
Average 99 stars, based on 1 article reviews
sir dna dye spirochrome - by Bioz Stars, 2026-10
99/100 stars
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5-sir-hoechst sted dna dye  (MatTek)
90
MatTek 5-sir-hoechst sted dna dye
A Western blots were performed on mitotic lysates generated from the panel of cell lines depleted of ZNF768 with inducible sh_ZNF768_1 ( n =3). B Representative immunofluorescence image of mitotic inducible HeLa cells after 48 hours doxycycline induction. Cells were stained for PLK1 (green), CENPC (grey) and with Hoechst (blue). C Quantification of the average relative intensity of PLK1 at kinetochores from ( B ) using previous inducible cancer cell lines ( n =3). D Representative stills of time-lapse movies of inducible HeLa cells after a 48 hours ZNF768 knockdown. For imaging, cells were synchronized in mitosis after release from a double thymidine block and incubated <t>with</t> <t>SiR-DNA</t> to visualize the chromatin. E Quantification of the average nuclear envelope breakdown to the anaphase onset duration in the indicated cell lines ( n = n=3 for all cell lines except for the HeLa, n=4). F Representative live cell images of mitotic defects observed after 48 hour ZNF768 depletion in HeLa cells. G Quantification of mitotic defects listed in F in MDA-MB-231, HeLa, HCT-116 and U87 cell lines after 48 hour ZNF768 depletion ( n =3). In all panels, data represent the mean ± SEM. In panel C , E and G , significance was determined by unpaired t test.
5 Sir Hoechst Sted Dna Dye, supplied by MatTek, 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/sir-dna+dye/5+sir+hoechst+sted+dna+dye/pm37113765-373-6-35
Average 90 stars, based on 1 article reviews
5-sir-hoechst sted dna dye - by Bioz Stars, 2026-10
90/100 stars
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dna loading dye  (Thermo Fisher)
96
Thermo Fisher dna loading dye
A Western blots were performed on mitotic lysates generated from the panel of cell lines depleted of ZNF768 with inducible sh_ZNF768_1 ( n =3). B Representative immunofluorescence image of mitotic inducible HeLa cells after 48 hours doxycycline induction. Cells were stained for PLK1 (green), CENPC (grey) and with Hoechst (blue). C Quantification of the average relative intensity of PLK1 at kinetochores from ( B ) using previous inducible cancer cell lines ( n =3). D Representative stills of time-lapse movies of inducible HeLa cells after a 48 hours ZNF768 knockdown. For imaging, cells were synchronized in mitosis after release from a double thymidine block and incubated <t>with</t> <t>SiR-DNA</t> to visualize the chromatin. E Quantification of the average nuclear envelope breakdown to the anaphase onset duration in the indicated cell lines ( n = n=3 for all cell lines except for the HeLa, n=4). F Representative live cell images of mitotic defects observed after 48 hour ZNF768 depletion in HeLa cells. G Quantification of mitotic defects listed in F in MDA-MB-231, HeLa, HCT-116 and U87 cell lines after 48 hour ZNF768 depletion ( n =3). In all panels, data represent the mean ± SEM. In panel C , E and G , significance was determined by unpaired t test.
Dna Loading Dye, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/sir-dna+dye/Agarose+Gel+Loading+Dye/pm33506682-59-12-15
Average 96 stars, based on 1 article reviews
dna loading dye - by Bioz Stars, 2026-10
96/100 stars
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dy-548-s-nhs-dye  (SIRS-Lab GmbH)
90
SIRS-Lab GmbH dy-548-s-nhs-dye
A Western blots were performed on mitotic lysates generated from the panel of cell lines depleted of ZNF768 with inducible sh_ZNF768_1 ( n =3). B Representative immunofluorescence image of mitotic inducible HeLa cells after 48 hours doxycycline induction. Cells were stained for PLK1 (green), CENPC (grey) and with Hoechst (blue). C Quantification of the average relative intensity of PLK1 at kinetochores from ( B ) using previous inducible cancer cell lines ( n =3). D Representative stills of time-lapse movies of inducible HeLa cells after a 48 hours ZNF768 knockdown. For imaging, cells were synchronized in mitosis after release from a double thymidine block and incubated <t>with</t> <t>SiR-DNA</t> to visualize the chromatin. E Quantification of the average nuclear envelope breakdown to the anaphase onset duration in the indicated cell lines ( n = n=3 for all cell lines except for the HeLa, n=4). F Representative live cell images of mitotic defects observed after 48 hour ZNF768 depletion in HeLa cells. G Quantification of mitotic defects listed in F in MDA-MB-231, HeLa, HCT-116 and U87 cell lines after 48 hour ZNF768 depletion ( n =3). In all panels, data represent the mean ± SEM. In panel C , E and G , significance was determined by unpaired t test.
Dy 548 S Nhs Dye, supplied by SIRS-Lab GmbH, 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/sir-dna+dye/dy+548+s+nhs+dye/10__1016_slash_j__ejmech__2017__09__021-214-11-28
Average 90 stars, based on 1 article reviews
dy-548-s-nhs-dye - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


A Western blots were performed on mitotic lysates generated from the panel of cell lines depleted of ZNF768 with inducible sh_ZNF768_1 ( n =3). B Representative immunofluorescence image of mitotic inducible HeLa cells after 48 hours doxycycline induction. Cells were stained for PLK1 (green), CENPC (grey) and with Hoechst (blue). C Quantification of the average relative intensity of PLK1 at kinetochores from ( B ) using previous inducible cancer cell lines ( n =3). D Representative stills of time-lapse movies of inducible HeLa cells after a 48 hours ZNF768 knockdown. For imaging, cells were synchronized in mitosis after release from a double thymidine block and incubated with SiR-DNA to visualize the chromatin. E Quantification of the average nuclear envelope breakdown to the anaphase onset duration in the indicated cell lines ( n = n=3 for all cell lines except for the HeLa, n=4). F Representative live cell images of mitotic defects observed after 48 hour ZNF768 depletion in HeLa cells. G Quantification of mitotic defects listed in F in MDA-MB-231, HeLa, HCT-116 and U87 cell lines after 48 hour ZNF768 depletion ( n =3). In all panels, data represent the mean ± SEM. In panel C , E and G , significance was determined by unpaired t test.

Journal: bioRxiv

Article Title: ZNF768 regulates expression of E2F1 protein to drive G0/G1 transition and cell cycle progression

doi: 10.64898/2026.08.03.742597

Figure Lengend Snippet: A Western blots were performed on mitotic lysates generated from the panel of cell lines depleted of ZNF768 with inducible sh_ZNF768_1 ( n =3). B Representative immunofluorescence image of mitotic inducible HeLa cells after 48 hours doxycycline induction. Cells were stained for PLK1 (green), CENPC (grey) and with Hoechst (blue). C Quantification of the average relative intensity of PLK1 at kinetochores from ( B ) using previous inducible cancer cell lines ( n =3). D Representative stills of time-lapse movies of inducible HeLa cells after a 48 hours ZNF768 knockdown. For imaging, cells were synchronized in mitosis after release from a double thymidine block and incubated with SiR-DNA to visualize the chromatin. E Quantification of the average nuclear envelope breakdown to the anaphase onset duration in the indicated cell lines ( n = n=3 for all cell lines except for the HeLa, n=4). F Representative live cell images of mitotic defects observed after 48 hour ZNF768 depletion in HeLa cells. G Quantification of mitotic defects listed in F in MDA-MB-231, HeLa, HCT-116 and U87 cell lines after 48 hour ZNF768 depletion ( n =3). In all panels, data represent the mean ± SEM. In panel C , E and G , significance was determined by unpaired t test.

Article Snippet: For live-cell imaging, cells were washed with PBS and treated with SiR-DNA dye (CY-SC007; Cytoskeleton) at 300 nM for 1 h prior to imaging.

Techniques: Western Blot, Generated, Immunofluorescence, Staining, Knockdown, Imaging, Blocking Assay, Incubation