annexin v pi staining Search Results


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Immunostep annexin-v–allophycocyanin (apc)/propidium iodide (pi) double staining
Annexin V–Allophycocyanin (Apc)/Propidium Iodide (Pi) Double Staining, supplied by Immunostep, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Nanjing Jiancheng Bioengineering Research Institute Co Ltd annexin v-fitc
Annexin V Fitc, supplied by Nanjing Jiancheng Bioengineering Research Institute Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Annexin V Fitc Apoptosis Kit, supplied by Joincare Pharmaceutical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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GraphPad Software Inc flow cytometry analysis with annexin v and pi double staining
Flow Cytometry Analysis With Annexin V And Pi Double Staining, supplied by GraphPad Software Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carl Roth GmbH annexin v-fitc/pi staining rotitest annexin v
Annexin V Fitc/Pi Staining Rotitest Annexin V, supplied by Carl Roth GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson annexin v/pi staining and flow cytometric analysis
Annexin V/Pi Staining And Flow Cytometric Analysis, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Imagenex Technology Corp annexin v/pi staining
Glutor exerts cytotoxic action on DL cells. DL cells or thymocytes (1 × 10 5 ) harvested from the thymi of healthy mice without tumor transplantation were processed for immunoblotting for GLUT1 and GLUT3 as described in the Materials and Methods section (A) . DL cells (1 × 10 5 ) were incubated in a medium alone or containing the indicated concentrations of glutor for 24 h (B, C) or with 0.01 µM of glutor for the various indicated time durations (D, E) , followed by estimation of cell viability by Trypan blue dye exclusion assay and cell survival by MTT assay as described in the Materials and Methods section. DL cells incubated in a medium alone or containing glutor (0.01 µM) for 24 h were examined for the mode of cell death by <t>Annexin</t> V/PI (H, I) and Wright–Giemsa (F, G) staining. Values shown in (B–E) and (G, I) are mean ± SD. The plates shown in (A) , (F) , and (H) are from a representative experiment out of at least two experiments with similar results. The bar diagram accompanying (A) is the densitometry of respective bands. * p < 0.05 vs. values of the respective control.
Annexin V/Pi Staining, supplied by Imagenex Technology Corp, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Jingxin Pharmaceutical Co Ltd annexin v-fitc/pi double staining apoptosis kit
Glutor exerts cytotoxic action on DL cells. DL cells or thymocytes (1 × 10 5 ) harvested from the thymi of healthy mice without tumor transplantation were processed for immunoblotting for GLUT1 and GLUT3 as described in the Materials and Methods section (A) . DL cells (1 × 10 5 ) were incubated in a medium alone or containing the indicated concentrations of glutor for 24 h (B, C) or with 0.01 µM of glutor for the various indicated time durations (D, E) , followed by estimation of cell viability by Trypan blue dye exclusion assay and cell survival by MTT assay as described in the Materials and Methods section. DL cells incubated in a medium alone or containing glutor (0.01 µM) for 24 h were examined for the mode of cell death by <t>Annexin</t> V/PI (H, I) and Wright–Giemsa (F, G) staining. Values shown in (B–E) and (G, I) are mean ± SD. The plates shown in (A) , (F) , and (H) are from a representative experiment out of at least two experiments with similar results. The bar diagram accompanying (A) is the densitometry of respective bands. * p < 0.05 vs. values of the respective control.
Annexin V Fitc/Pi Double Staining Apoptosis Kit, supplied by Jingxin Pharmaceutical Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MBL Life science annexin v pi staining
Glutor exerts cytotoxic action on DL cells. DL cells or thymocytes (1 × 10 5 ) harvested from the thymi of healthy mice without tumor transplantation were processed for immunoblotting for GLUT1 and GLUT3 as described in the Materials and Methods section (A) . DL cells (1 × 10 5 ) were incubated in a medium alone or containing the indicated concentrations of glutor for 24 h (B, C) or with 0.01 µM of glutor for the various indicated time durations (D, E) , followed by estimation of cell viability by Trypan blue dye exclusion assay and cell survival by MTT assay as described in the Materials and Methods section. DL cells incubated in a medium alone or containing glutor (0.01 µM) for 24 h were examined for the mode of cell death by <t>Annexin</t> V/PI (H, I) and Wright–Giemsa (F, G) staining. Values shown in (B–E) and (G, I) are mean ± SD. The plates shown in (A) , (F) , and (H) are from a representative experiment out of at least two experiments with similar results. The bar diagram accompanying (A) is the densitometry of respective bands. * p < 0.05 vs. values of the respective control.
Annexin V Pi Staining, supplied by MBL Life science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Becton Dickinson flow cytometer with annexin v– fitc and pi double staining
Glutor exerts cytotoxic action on DL cells. DL cells or thymocytes (1 × 10 5 ) harvested from the thymi of healthy mice without tumor transplantation were processed for immunoblotting for GLUT1 and GLUT3 as described in the Materials and Methods section (A) . DL cells (1 × 10 5 ) were incubated in a medium alone or containing the indicated concentrations of glutor for 24 h (B, C) or with 0.01 µM of glutor for the various indicated time durations (D, E) , followed by estimation of cell viability by Trypan blue dye exclusion assay and cell survival by MTT assay as described in the Materials and Methods section. DL cells incubated in a medium alone or containing glutor (0.01 µM) for 24 h were examined for the mode of cell death by <t>Annexin</t> V/PI (H, I) and Wright–Giemsa (F, G) staining. Values shown in (B–E) and (G, I) are mean ± SD. The plates shown in (A) , (F) , and (H) are from a representative experiment out of at least two experiments with similar results. The bar diagram accompanying (A) is the densitometry of respective bands. * p < 0.05 vs. values of the respective control.
Flow Cytometer With Annexin V– Fitc And Pi Double Staining, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cambridge Bioscience annexin-v/propidium iodide (pi) staining
Glutor exerts cytotoxic action on DL cells. DL cells or thymocytes (1 × 10 5 ) harvested from the thymi of healthy mice without tumor transplantation were processed for immunoblotting for GLUT1 and GLUT3 as described in the Materials and Methods section (A) . DL cells (1 × 10 5 ) were incubated in a medium alone or containing the indicated concentrations of glutor for 24 h (B, C) or with 0.01 µM of glutor for the various indicated time durations (D, E) , followed by estimation of cell viability by Trypan blue dye exclusion assay and cell survival by MTT assay as described in the Materials and Methods section. DL cells incubated in a medium alone or containing glutor (0.01 µM) for 24 h were examined for the mode of cell death by <t>Annexin</t> V/PI (H, I) and Wright–Giemsa (F, G) staining. Values shown in (B–E) and (G, I) are mean ± SD. The plates shown in (A) , (F) , and (H) are from a representative experiment out of at least two experiments with similar results. The bar diagram accompanying (A) is the densitometry of respective bands. * p < 0.05 vs. values of the respective control.
Annexin V/Propidium Iodide (Pi) Staining, supplied by Cambridge Bioscience, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Genechem annexin v-fitc detection kit
Glutor exerts cytotoxic action on DL cells. DL cells or thymocytes (1 × 10 5 ) harvested from the thymi of healthy mice without tumor transplantation were processed for immunoblotting for GLUT1 and GLUT3 as described in the Materials and Methods section (A) . DL cells (1 × 10 5 ) were incubated in a medium alone or containing the indicated concentrations of glutor for 24 h (B, C) or with 0.01 µM of glutor for the various indicated time durations (D, E) , followed by estimation of cell viability by Trypan blue dye exclusion assay and cell survival by MTT assay as described in the Materials and Methods section. DL cells incubated in a medium alone or containing glutor (0.01 µM) for 24 h were examined for the mode of cell death by <t>Annexin</t> V/PI (H, I) and Wright–Giemsa (F, G) staining. Values shown in (B–E) and (G, I) are mean ± SD. The plates shown in (A) , (F) , and (H) are from a representative experiment out of at least two experiments with similar results. The bar diagram accompanying (A) is the densitometry of respective bands. * p < 0.05 vs. values of the respective control.
Annexin V Fitc Detection Kit, supplied by Genechem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Glutor exerts cytotoxic action on DL cells. DL cells or thymocytes (1 × 10 5 ) harvested from the thymi of healthy mice without tumor transplantation were processed for immunoblotting for GLUT1 and GLUT3 as described in the Materials and Methods section (A) . DL cells (1 × 10 5 ) were incubated in a medium alone or containing the indicated concentrations of glutor for 24 h (B, C) or with 0.01 µM of glutor for the various indicated time durations (D, E) , followed by estimation of cell viability by Trypan blue dye exclusion assay and cell survival by MTT assay as described in the Materials and Methods section. DL cells incubated in a medium alone or containing glutor (0.01 µM) for 24 h were examined for the mode of cell death by Annexin V/PI (H, I) and Wright–Giemsa (F, G) staining. Values shown in (B–E) and (G, I) are mean ± SD. The plates shown in (A) , (F) , and (H) are from a representative experiment out of at least two experiments with similar results. The bar diagram accompanying (A) is the densitometry of respective bands. * p < 0.05 vs. values of the respective control.

Journal: Frontiers in Oncology

Article Title: Glutor, a Glucose Transporter Inhibitor, Exerts Antineoplastic Action on Tumor Cells of Thymic Origin: Implication of Modulated Metabolism, Survival, Oxidative Stress, Mitochondrial Membrane Potential, pH Homeostasis, and Chemosensitivity

doi: 10.3389/fonc.2022.925666

Figure Lengend Snippet: Glutor exerts cytotoxic action on DL cells. DL cells or thymocytes (1 × 10 5 ) harvested from the thymi of healthy mice without tumor transplantation were processed for immunoblotting for GLUT1 and GLUT3 as described in the Materials and Methods section (A) . DL cells (1 × 10 5 ) were incubated in a medium alone or containing the indicated concentrations of glutor for 24 h (B, C) or with 0.01 µM of glutor for the various indicated time durations (D, E) , followed by estimation of cell viability by Trypan blue dye exclusion assay and cell survival by MTT assay as described in the Materials and Methods section. DL cells incubated in a medium alone or containing glutor (0.01 µM) for 24 h were examined for the mode of cell death by Annexin V/PI (H, I) and Wright–Giemsa (F, G) staining. Values shown in (B–E) and (G, I) are mean ± SD. The plates shown in (A) , (F) , and (H) are from a representative experiment out of at least two experiments with similar results. The bar diagram accompanying (A) is the densitometry of respective bands. * p < 0.05 vs. values of the respective control.

Article Snippet: Annexin V/PI staining was carried out following the manufacturer’s instructions (Imagenex USA).

Techniques: Transplantation Assay, Western Blot, Incubation, Exclusion Assay, MTT Assay, Staining, Control