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red fluorescent dextran  (Thermo Fisher)
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Thermo Fisher red fluorescent dextran
Red Fluorescent Dextran, 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
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mitosox red fluorescent probe  (MedChemExpress)
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Conditional knockout of ZnT3 inhibited the phosphorylation of STAT3 in induced mitochondrial apoptosis in cerebral ischemia/reperfusion mice. (A, B) Western blot analysis of p‐STAT3 expression in isolated mitochondria from ZnT3‐cKO or control mice after 60‐min ischemia followed by 24‐h reperfusion ( n = 6 per group). (C) Representative JC‐1 red fluorescence images showing mitochondrial membrane potential in mitochondria isolated from ischemic hemisphere. Scale bar: 100 μm. (D) Quantification of JC‐1 red/green fluorescence ratio in mitochondria isolated from ischemic hemisphere ( n = 3 per group). (E) Quantitative analysis of mitochondrial ROS levels assessed by <t>MitoSOX</t> staining ( n = 3 per group). (F, G) Western blot analysis of Cytochrome C (Cyt C) expression in brain mitochondria from ZnT3‐cKO or control mice with or without ZnCl 2 treatment ( n = 6 per group). Data were presented as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 versus Control + Saline; #### p < 0.0001 versus cKO + Saline.
Mitosox Red Fluorescent Probe, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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red fluorescent cell membrane dye did  (Shanghai Titan Scientific)
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Shanghai Titan Scientific red fluorescent cell membrane dye did
Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal <t>fluorescent</t> images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Red Fluorescent Cell Membrane Dye Did, supplied by Shanghai Titan Scientific, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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red fluorescence  (Servicebio Inc)
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Servicebio Inc red fluorescence
Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal <t>fluorescent</t> images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Red Fluorescence, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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red fluorescence  (Beyotime)
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Beyotime red fluorescence
Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal <t>fluorescent</t> images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Red Fluorescence, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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lipid droplets red fluorescence assay kit  (Beyotime)
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Beyotime lipid droplets red fluorescence assay kit
Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal <t>fluorescent</t> images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Lipid Droplets Red Fluorescence Assay Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mitosox red fluorescence  (Beyotime)
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Beyotime mitosox red fluorescence
Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal <t>fluorescent</t> images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Mitosox Red Fluorescence, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescent probe mitosox red  (MedChemExpress)
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MedChemExpress fluorescent probe mitosox red
Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal <t>fluorescent</t> images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Fluorescent Probe Mitosox Red, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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superoxide red fluorescent probe  (Yeasen Biotechnology)
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Yeasen Biotechnology superoxide red fluorescent probe
Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal <t>fluorescent</t> images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)
Superoxide Red Fluorescent Probe, supplied by Yeasen Biotechnology, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Conditional knockout of ZnT3 inhibited the phosphorylation of STAT3 in induced mitochondrial apoptosis in cerebral ischemia/reperfusion mice. (A, B) Western blot analysis of p‐STAT3 expression in isolated mitochondria from ZnT3‐cKO or control mice after 60‐min ischemia followed by 24‐h reperfusion ( n = 6 per group). (C) Representative JC‐1 red fluorescence images showing mitochondrial membrane potential in mitochondria isolated from ischemic hemisphere. Scale bar: 100 μm. (D) Quantification of JC‐1 red/green fluorescence ratio in mitochondria isolated from ischemic hemisphere ( n = 3 per group). (E) Quantitative analysis of mitochondrial ROS levels assessed by MitoSOX staining ( n = 3 per group). (F, G) Western blot analysis of Cytochrome C (Cyt C) expression in brain mitochondria from ZnT3‐cKO or control mice with or without ZnCl 2 treatment ( n = 6 per group). Data were presented as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 versus Control + Saline; #### p < 0.0001 versus cKO + Saline.

Journal: CNS Neuroscience & Therapeutics

Article Title: Zinc Overload in Microvessels Contributes to Blood–Brain Barrier Disruption by Activating the JAK2 Pathway After Cerebral Ischemia/Reperfusion

doi: 10.1002/cns.70885

Figure Lengend Snippet: Conditional knockout of ZnT3 inhibited the phosphorylation of STAT3 in induced mitochondrial apoptosis in cerebral ischemia/reperfusion mice. (A, B) Western blot analysis of p‐STAT3 expression in isolated mitochondria from ZnT3‐cKO or control mice after 60‐min ischemia followed by 24‐h reperfusion ( n = 6 per group). (C) Representative JC‐1 red fluorescence images showing mitochondrial membrane potential in mitochondria isolated from ischemic hemisphere. Scale bar: 100 μm. (D) Quantification of JC‐1 red/green fluorescence ratio in mitochondria isolated from ischemic hemisphere ( n = 3 per group). (E) Quantitative analysis of mitochondrial ROS levels assessed by MitoSOX staining ( n = 3 per group). (F, G) Western blot analysis of Cytochrome C (Cyt C) expression in brain mitochondria from ZnT3‐cKO or control mice with or without ZnCl 2 treatment ( n = 6 per group). Data were presented as mean ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 versus Control + Saline; #### p < 0.0001 versus cKO + Saline.

Article Snippet: Mitochondrial superoxide levels were detected using the MitoSOX Red fluorescent probe (MedChemExpress) [ ].

Techniques: Knock-Out, Phospho-proteomics, Western Blot, Expressing, Isolation, Control, Fluorescence, Membrane, Staining, Saline

Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal fluorescent images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Journal: International Journal of Pharmaceutics: X

Article Title: Allicin-based biomimetic nanoparticles of the erythrocyte membrane for the delivery of lumefantrine to enhance its antimalarial effect

doi: 10.1016/j.ijpx.2026.100487

Figure Lengend Snippet: Neutralization of merozoites. A Purification of infected erythrocytes using the Percoll separation solution, displaying infected (black arrow) and normal (red arrow) erythrocytes. B Confocal fluorescent images of merozoites (blue), PECm-Allicin@LM (red), and their colocalization (purple). Scale bar = 50 μm. C Representative scatter plots of Hoechst 33342/CFDA-SE for the invasion test of merozoites and normal erythrocytes after drug treatment. D Intrusion rate (the percentage of cells in the Q2 area in each group relative to that in the Q2 area in the Model group). Data are presented as mean ± SEM ( n = 3), * P < 0.05. (For interpretation of the references to colour in this figure legend, the reader is referred to the web version of this article.)

Article Snippet: The red fluorescent cell membrane dye DiD was purchased from Shanghai Titan Scientific Co., Ltd. (China).

Techniques: Neutralization, Purification, Infection