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id7000 system software  (Sony Biotechnology)
99
Sony Biotechnology id7000 system software
Figure 6. Honey treatment induces apoptosis in PanCa cells. (A). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in MIA PaCa-2 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (B). Representative flow cytometry micrographs showing apoptosis in MIA PaCa-2 cells treated with honey for 24 h. The Annexin V/PI-stained cells were analyzed on SONY’ <t>ID7000</t> Spectral Cell Analyzer. Three independent runs were recorded for each treatment group. (C). The bar graph represents quantification of live, early, and late apoptotic MIA PaCa-2 cells. The data in the bar graph represent the % count ± SEM of three replicates of each dose of honey. Level of significance: ns p = 0.4234; ** p < 0.0027; *** p < 0.0004; **** p < 0.0001. (D). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in AsPC-1 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (E). Representative flow cytometry micrographs showing
Id7000 System Software, supplied by Sony Biotechnology, 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/id7000+software/ID7000+Spectral+Cell+Analyzer/pm39410048-135-7-11
Average 99 stars, based on 1 article reviews
id7000 system software - by Bioz Stars, 2026-09
99/100 stars
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id7000 spectral cell analyzer (equipped with the id7000 software version 1.1.8.18211)  (Sony)
90
Sony id7000 spectral cell analyzer (equipped with the id7000 software version 1.1.8.18211)
Figure 6. Honey treatment induces apoptosis in PanCa cells. (A). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in MIA PaCa-2 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (B). Representative flow cytometry micrographs showing apoptosis in MIA PaCa-2 cells treated with honey for 24 h. The Annexin V/PI-stained cells were analyzed on SONY’ <t>ID7000</t> Spectral Cell Analyzer. Three independent runs were recorded for each treatment group. (C). The bar graph represents quantification of live, early, and late apoptotic MIA PaCa-2 cells. The data in the bar graph represent the % count ± SEM of three replicates of each dose of honey. Level of significance: ns p = 0.4234; ** p < 0.0027; *** p < 0.0004; **** p < 0.0001. (D). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in AsPC-1 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (E). Representative flow cytometry micrographs showing
Id7000 Spectral Cell Analyzer (Equipped With The Id7000 Software Version 1.1.8.18211), supplied by Sony, 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/id7000+software/sh800+cell+sorter/pmc11598761-86-22-33
Average 90 stars, based on 1 article reviews
id7000 spectral cell analyzer (equipped with the id7000 software version 1.1.8.18211) - by Bioz Stars, 2026-09
90/100 stars
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instruments id7000 spectral cell analyzer tc20tm data analyzer software biorad  (Bio-Rad)
99
Bio-Rad instruments id7000 spectral cell analyzer tc20tm data analyzer software biorad
Figure 6. Honey treatment induces apoptosis in PanCa cells. (A). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in MIA PaCa-2 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (B). Representative flow cytometry micrographs showing apoptosis in MIA PaCa-2 cells treated with honey for 24 h. The Annexin V/PI-stained cells were analyzed on SONY’ <t>ID7000</t> Spectral Cell Analyzer. Three independent runs were recorded for each treatment group. (C). The bar graph represents quantification of live, early, and late apoptotic MIA PaCa-2 cells. The data in the bar graph represent the % count ± SEM of three replicates of each dose of honey. Level of significance: ns p = 0.4234; ** p < 0.0027; *** p < 0.0004; **** p < 0.0001. (D). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in AsPC-1 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (E). Representative flow cytometry micrographs showing
Instruments Id7000 Spectral Cell Analyzer Tc20tm Data Analyzer Software Biorad, supplied by Bio-Rad, 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/id7000+software/TC20+Data+Analyzer+Software/pm41422505-350-129-134
Average 99 stars, based on 1 article reviews
instruments id7000 spectral cell analyzer tc20tm data analyzer software biorad - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier

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Figure 6. Honey treatment induces apoptosis in PanCa cells. (A). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in MIA PaCa-2 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (B). Representative flow cytometry micrographs showing apoptosis in MIA PaCa-2 cells treated with honey for 24 h. The Annexin V/PI-stained cells were analyzed on SONY’ ID7000 Spectral Cell Analyzer. Three independent runs were recorded for each treatment group. (C). The bar graph represents quantification of live, early, and late apoptotic MIA PaCa-2 cells. The data in the bar graph represent the % count ± SEM of three replicates of each dose of honey. Level of significance: ns p = 0.4234; ** p < 0.0027; *** p < 0.0004; **** p < 0.0001. (D). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in AsPC-1 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (E). Representative flow cytometry micrographs showing

Journal: Cancers

Article Title: Honey Targets Ribosome Biogenesis Components to Suppress the Growth of Human Pancreatic Cancer Cells.

doi: 10.3390/cancers16193431

Figure Lengend Snippet: Figure 6. Honey treatment induces apoptosis in PanCa cells. (A). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in MIA PaCa-2 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (B). Representative flow cytometry micrographs showing apoptosis in MIA PaCa-2 cells treated with honey for 24 h. The Annexin V/PI-stained cells were analyzed on SONY’ ID7000 Spectral Cell Analyzer. Three independent runs were recorded for each treatment group. (C). The bar graph represents quantification of live, early, and late apoptotic MIA PaCa-2 cells. The data in the bar graph represent the % count ± SEM of three replicates of each dose of honey. Level of significance: ns p = 0.4234; ** p < 0.0027; *** p < 0.0004; **** p < 0.0001. (D). Effect of honey on protein levels of mutant p53, Bcl-2, caspase-3, and PARP in AsPC-1 cells as determined using Western blot analysis after 24 h of honey exposure. Equal loading of protein in each lane was assessed by probing the blots with β-actin antibody. (E). Representative flow cytometry micrographs showing

Article Snippet: The data generated were analyzed using the ID7000 system software by SONY.

Techniques: Mutagenesis, Western Blot, Flow Cytometry, Staining