Review





Similar Products

flow cytometric analysis  (Miltenyi Biotec)
98
Miltenyi Biotec flow cytometric analysis
Flow Cytometric Analysis, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/flow+cytometric+analysis/MACSQuant+Analyzer+10/pmc13236643-57-0-12
Average 98 stars, based on 1 article reviews
flow cytometric analysis - by Bioz Stars, 2026-09
98/100 stars
  Buy from Supplier
flow cytometric analysis fluorescent monoclonal antibody kit  (Tongsheng Inc)
86
Tongsheng Inc flow cytometric analysis fluorescent monoclonal antibody kit
Flow Cytometric Analysis Fluorescent Monoclonal Antibody Kit, supplied by Tongsheng Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/flow+cytometric+analysis/analysis+antibody+cytometric+flow+fluorescent+kit+monoclonal/pm42117705-141-48-55
Average 86 stars, based on 1 article reviews
flow cytometric analysis fluorescent monoclonal antibody kit - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier
flow cytometric analysis  (Tree Star Inc)
86
Tree Star Inc flow cytometric analysis
Characterization, cytotoxicity, uptake, and drug release of biomimetic liposomes. (A, B) Mean diameter (A) and Zeta potential (B) of PLip ( n = 3). (C) The representative Cryo-EM image depicted PLip laden with gambogic acid. Scale bar = 100 nm. (D) CCK-8 assay to evaluate the viability of 4T1 cells after various treatments ( n = 3). (E, F) Representative flow cytometry plots depicting apoptosis in tumor cells following various treatments (F), along with a corresponding statistical graph of late apoptosis (E) ( n = 3). (G, H) Observations of cellular uptake of DiD-labeled liposomes under various treatments using fluorescence confocal microscopy (G, scale bar = 20 μm), and flow <t>cytometric</t> quantification (H) ( n = 3). (I) Alterations of CD44 protein expression in tumor cells following HIFU treatment ( n = 3). (J) Comparison of PLip’s drug release profile in high H 2 O 2 conditions versus an H 2 O 2 -free environment ( n = 3). (K, L) Intracellular (K) and extracellular (L) H 2 O 2 levels following various treatments ( n = 3). Data are presented as mean ± SD. Statistical significance was analyzed by one-way ANOVA with a Tukey post hoc test. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ∗∗∗∗ P < 0.0001 vs. indicated; ns, no significance.
Flow Cytometric Analysis, supplied by Tree Star Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/flow+cytometric+analysis/analysis+cytometric+flow/pmc13198351-141-1-12
Average 86 stars, based on 1 article reviews
flow cytometric analysis - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier
firoozabady e rapid flow cytometric analysis  (Galbraith Laboratories Inc)
86
Galbraith Laboratories Inc firoozabady e rapid flow cytometric analysis
Characterization, cytotoxicity, uptake, and drug release of biomimetic liposomes. (A, B) Mean diameter (A) and Zeta potential (B) of PLip ( n = 3). (C) The representative Cryo-EM image depicted PLip laden with gambogic acid. Scale bar = 100 nm. (D) CCK-8 assay to evaluate the viability of 4T1 cells after various treatments ( n = 3). (E, F) Representative flow cytometry plots depicting apoptosis in tumor cells following various treatments (F), along with a corresponding statistical graph of late apoptosis (E) ( n = 3). (G, H) Observations of cellular uptake of DiD-labeled liposomes under various treatments using fluorescence confocal microscopy (G, scale bar = 20 μm), and flow <t>cytometric</t> quantification (H) ( n = 3). (I) Alterations of CD44 protein expression in tumor cells following HIFU treatment ( n = 3). (J) Comparison of PLip’s drug release profile in high H 2 O 2 conditions versus an H 2 O 2 -free environment ( n = 3). (K, L) Intracellular (K) and extracellular (L) H 2 O 2 levels following various treatments ( n = 3). Data are presented as mean ± SD. Statistical significance was analyzed by one-way ANOVA with a Tukey post hoc test. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ∗∗∗∗ P < 0.0001 vs. indicated; ns, no significance.
Firoozabady E Rapid Flow Cytometric Analysis, supplied by Galbraith Laboratories Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/flow+cytometric+analysis/analysis+cytometric+e+firoozabady+flow+rapid/pm42050625-540-10-0
Average 86 stars, based on 1 article reviews
firoozabady e rapid flow cytometric analysis - by Bioz Stars, 2026-09
86/100 stars
  Buy from Supplier
sh800 cell sorter  (Sony Biotechnology)
99
Sony Biotechnology sh800 cell sorter
Characterization, cytotoxicity, uptake, and drug release of biomimetic liposomes. (A, B) Mean diameter (A) and Zeta potential (B) of PLip ( n = 3). (C) The representative Cryo-EM image depicted PLip laden with gambogic acid. Scale bar = 100 nm. (D) CCK-8 assay to evaluate the viability of 4T1 cells after various treatments ( n = 3). (E, F) Representative flow cytometry plots depicting apoptosis in tumor cells following various treatments (F), along with a corresponding statistical graph of late apoptosis (E) ( n = 3). (G, H) Observations of cellular uptake of DiD-labeled liposomes under various treatments using fluorescence confocal microscopy (G, scale bar = 20 μm), and flow <t>cytometric</t> quantification (H) ( n = 3). (I) Alterations of CD44 protein expression in tumor cells following HIFU treatment ( n = 3). (J) Comparison of PLip’s drug release profile in high H 2 O 2 conditions versus an H 2 O 2 -free environment ( n = 3). (K, L) Intracellular (K) and extracellular (L) H 2 O 2 levels following various treatments ( n = 3). Data are presented as mean ± SD. Statistical significance was analyzed by one-way ANOVA with a Tukey post hoc test. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ∗∗∗∗ P < 0.0001 vs. indicated; ns, no significance.
Sh800 Cell Sorter, 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/flow+cytometric+analysis/SH800+Cell+Sorter/custom%40sh800%4042014878
Average 99 stars, based on 1 article reviews
sh800 cell sorter - by Bioz Stars, 2026-09
99/100 stars
  Buy from Supplier

Image Search Results


Characterization, cytotoxicity, uptake, and drug release of biomimetic liposomes. (A, B) Mean diameter (A) and Zeta potential (B) of PLip ( n = 3). (C) The representative Cryo-EM image depicted PLip laden with gambogic acid. Scale bar = 100 nm. (D) CCK-8 assay to evaluate the viability of 4T1 cells after various treatments ( n = 3). (E, F) Representative flow cytometry plots depicting apoptosis in tumor cells following various treatments (F), along with a corresponding statistical graph of late apoptosis (E) ( n = 3). (G, H) Observations of cellular uptake of DiD-labeled liposomes under various treatments using fluorescence confocal microscopy (G, scale bar = 20 μm), and flow cytometric quantification (H) ( n = 3). (I) Alterations of CD44 protein expression in tumor cells following HIFU treatment ( n = 3). (J) Comparison of PLip’s drug release profile in high H 2 O 2 conditions versus an H 2 O 2 -free environment ( n = 3). (K, L) Intracellular (K) and extracellular (L) H 2 O 2 levels following various treatments ( n = 3). Data are presented as mean ± SD. Statistical significance was analyzed by one-way ANOVA with a Tukey post hoc test. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ∗∗∗∗ P < 0.0001 vs. indicated; ns, no significance.

Journal: Acta Pharmaceutica Sinica. B

Article Title: Biomimetic liposomes synergize with high-intensity focused ultrasound to induce ferroptosis in tumors

doi: 10.1016/j.apsb.2026.02.024

Figure Lengend Snippet: Characterization, cytotoxicity, uptake, and drug release of biomimetic liposomes. (A, B) Mean diameter (A) and Zeta potential (B) of PLip ( n = 3). (C) The representative Cryo-EM image depicted PLip laden with gambogic acid. Scale bar = 100 nm. (D) CCK-8 assay to evaluate the viability of 4T1 cells after various treatments ( n = 3). (E, F) Representative flow cytometry plots depicting apoptosis in tumor cells following various treatments (F), along with a corresponding statistical graph of late apoptosis (E) ( n = 3). (G, H) Observations of cellular uptake of DiD-labeled liposomes under various treatments using fluorescence confocal microscopy (G, scale bar = 20 μm), and flow cytometric quantification (H) ( n = 3). (I) Alterations of CD44 protein expression in tumor cells following HIFU treatment ( n = 3). (J) Comparison of PLip’s drug release profile in high H 2 O 2 conditions versus an H 2 O 2 -free environment ( n = 3). (K, L) Intracellular (K) and extracellular (L) H 2 O 2 levels following various treatments ( n = 3). Data are presented as mean ± SD. Statistical significance was analyzed by one-way ANOVA with a Tukey post hoc test. ∗ P < 0.05, ∗∗ P < 0.01, ∗∗∗ P < 0.001, ∗∗∗∗ P < 0.0001 vs. indicated; ns, no significance.

Article Snippet: Subsequently, flow cytometric analysis was performed on the cells using FlowJo v.7.6.5 (Tree Star, Inc., Ashland, USA).

Techniques: Liposomes, Zeta Potential Analyzer, Cryo-EM Sample Prep, CCK-8 Assay, Flow Cytometry, Labeling, Fluorescence, Confocal Microscopy, Expressing, Comparison