annexin v fitc propidium iodide pi dual staining kit Search Results


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Flow Cytometry Using Annexin V Fluoroisothiocyanate (Fitc)/Propidium Iodide (Pi) Kit, 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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Sony fluorochrome-labelled annexin v (fitc) and propidium iodide (pi) staining kit
Fluorochrome Labelled Annexin V (Fitc) And Propidium Iodide (Pi) Staining Kit, 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
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Annexin V Fitc/Propidium Iodide (Pi) Kit, supplied by MD Biosciences, 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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Dex treatment suppressed miR-375 expression and the viability of 9HTE cells, and promoted <t>apoptosis</t> in a time-dependent manner. (A) Cell viability following Dex pre-treatment for different periods of time (0, 6, 12 and 24 h) followed by incubation for a further 12 or 24 h detected using Cell Counting Kit-8 assay. (B and C) Cell apoptotic rate following Dex treatment for different periods of time (0, 6, 12 and 24 h) detected using flow cytometry. (D) Relative expression levels of miR-375, miR-let-7, miR-21, miR-19 and miR-455 in cells following Dex treatment for different periods of time (0, 6, 12 and 24 h) measured using reverse transcription-quantitative PCR. U6 was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. * P<0.05, ** P<0.01 and *** P<0.001 vs. Dex 0 h. Dex, dexamethasone.
Annexin V Fitc/Propidium Iodide (Pi) Apoptosis Kit A211, supplied by GeneBio Systems 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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Becton Dickinson apoptosis detection kit containing annexinv-fitc propidium iodide (pi
Dex treatment suppressed miR-375 expression and the viability of 9HTE cells, and promoted <t>apoptosis</t> in a time-dependent manner. (A) Cell viability following Dex pre-treatment for different periods of time (0, 6, 12 and 24 h) followed by incubation for a further 12 or 24 h detected using Cell Counting Kit-8 assay. (B and C) Cell apoptotic rate following Dex treatment for different periods of time (0, 6, 12 and 24 h) detected using flow cytometry. (D) Relative expression levels of miR-375, miR-let-7, miR-21, miR-19 and miR-455 in cells following Dex treatment for different periods of time (0, 6, 12 and 24 h) measured using reverse transcription-quantitative PCR. U6 was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. * P<0.05, ** P<0.01 and *** P<0.001 vs. Dex 0 h. Dex, dexamethasone.
Apoptosis Detection Kit Containing Annexinv Fitc Propidium Iodide (Pi, 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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Becton Dickinson human annexinv-fitc (av) and propidium iodide (pi) detection kit
Dex treatment suppressed miR-375 expression and the viability of 9HTE cells, and promoted <t>apoptosis</t> in a time-dependent manner. (A) Cell viability following Dex pre-treatment for different periods of time (0, 6, 12 and 24 h) followed by incubation for a further 12 or 24 h detected using Cell Counting Kit-8 assay. (B and C) Cell apoptotic rate following Dex treatment for different periods of time (0, 6, 12 and 24 h) detected using flow cytometry. (D) Relative expression levels of miR-375, miR-let-7, miR-21, miR-19 and miR-455 in cells following Dex treatment for different periods of time (0, 6, 12 and 24 h) measured using reverse transcription-quantitative PCR. U6 was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. * P<0.05, ** P<0.01 and *** P<0.001 vs. Dex 0 h. Dex, dexamethasone.
Human Annexinv Fitc (Av) And Propidium Iodide (Pi) Detection Kit, 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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MultiSciences Biotech Co Ltd anxa5/annexin v-fitc propidium iodide/pi apoptosis detection kit
Dex treatment suppressed miR-375 expression and the viability of 9HTE cells, and promoted <t>apoptosis</t> in a time-dependent manner. (A) Cell viability following Dex pre-treatment for different periods of time (0, 6, 12 and 24 h) followed by incubation for a further 12 or 24 h detected using Cell Counting Kit-8 assay. (B and C) Cell apoptotic rate following Dex treatment for different periods of time (0, 6, 12 and 24 h) detected using flow cytometry. (D) Relative expression levels of miR-375, miR-let-7, miR-21, miR-19 and miR-455 in cells following Dex treatment for different periods of time (0, 6, 12 and 24 h) measured using reverse transcription-quantitative PCR. U6 was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. * P<0.05, ** P<0.01 and *** P<0.001 vs. Dex 0 h. Dex, dexamethasone.
Anxa5/Annexin V Fitc Propidium Iodide/Pi Apoptosis Detection Kit, supplied by MultiSciences Biotech 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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Beijing Chemclin Biotech Co annexin v-fluorescein isothiocyanate (fitc)/propidium iodide (pi) apoptosis detection kit
CTD induces apoptosis in A549 cells. (A) Flow cytometric analysis of A549 cell apoptosis by double staining with <t>Annexin</t> V-FITC and propidium iodide (PI). (B) The protein expression of Bax, Bcl-2, active caspase-3 were determined by western blotting. The protein expression of GAPDH was as used as the internal control. The protein expressions were quantified for (C) Bcl-2, (D) Bax and (E) active caspase-3. Images were analyzed by Image-Pro Plus 6.0 software. Results are presented as the mean ± standard deviation of three independent experiments. *P<0.05 was considered to indicate a statistically significantly difference vs. NC groups. Bcl-2, B-cell lymphoma-2; Bax, Bcl-associated X; CTD, cantharidin; FITC, fluorescein <t>isothiocyanate;</t> NC, negative control.
Annexin V Fluorescein Isothiocyanate (Fitc)/Propidium Iodide (Pi) Apoptosis Detection Kit, supplied by Beijing Chemclin Biotech Co, 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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Vazyme Biotech Co annexin v-fitc pi apoptosis detection kit
CTD induces apoptosis in A549 cells. (A) Flow cytometric analysis of A549 cell apoptosis by double staining with <t>Annexin</t> V-FITC and propidium iodide (PI). (B) The protein expression of Bax, Bcl-2, active caspase-3 were determined by western blotting. The protein expression of GAPDH was as used as the internal control. The protein expressions were quantified for (C) Bcl-2, (D) Bax and (E) active caspase-3. Images were analyzed by Image-Pro Plus 6.0 software. Results are presented as the mean ± standard deviation of three independent experiments. *P<0.05 was considered to indicate a statistically significantly difference vs. NC groups. Bcl-2, B-cell lymphoma-2; Bax, Bcl-associated X; CTD, cantharidin; FITC, fluorescein <t>isothiocyanate;</t> NC, negative control.
Annexin V Fitc Pi Apoptosis Detection Kit, supplied by Vazyme Biotech Co, 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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Image Search Results


Dex treatment suppressed miR-375 expression and the viability of 9HTE cells, and promoted apoptosis in a time-dependent manner. (A) Cell viability following Dex pre-treatment for different periods of time (0, 6, 12 and 24 h) followed by incubation for a further 12 or 24 h detected using Cell Counting Kit-8 assay. (B and C) Cell apoptotic rate following Dex treatment for different periods of time (0, 6, 12 and 24 h) detected using flow cytometry. (D) Relative expression levels of miR-375, miR-let-7, miR-21, miR-19 and miR-455 in cells following Dex treatment for different periods of time (0, 6, 12 and 24 h) measured using reverse transcription-quantitative PCR. U6 was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. * P<0.05, ** P<0.01 and *** P<0.001 vs. Dex 0 h. Dex, dexamethasone.

Journal: International Journal of Molecular Medicine

Article Title: Overexpression of miR-375 reverses the effects of dexamethasone on the viability, migration, invasion and apoptosis of human airway epithelial cells by targeting DUSP6

doi: 10.3892/ijmm.2022.5081

Figure Lengend Snippet: Dex treatment suppressed miR-375 expression and the viability of 9HTE cells, and promoted apoptosis in a time-dependent manner. (A) Cell viability following Dex pre-treatment for different periods of time (0, 6, 12 and 24 h) followed by incubation for a further 12 or 24 h detected using Cell Counting Kit-8 assay. (B and C) Cell apoptotic rate following Dex treatment for different periods of time (0, 6, 12 and 24 h) detected using flow cytometry. (D) Relative expression levels of miR-375, miR-let-7, miR-21, miR-19 and miR-455 in cells following Dex treatment for different periods of time (0, 6, 12 and 24 h) measured using reverse transcription-quantitative PCR. U6 was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. * P<0.05, ** P<0.01 and *** P<0.001 vs. Dex 0 h. Dex, dexamethasone.

Article Snippet: 9HTE cell apoptosis was detected using flow cytometry with an Annexin V-FITC/propidium iodide (PI) apoptosis kit (A211; GeneBio Systems, Inc.) as per the manufacturer's instructions.

Techniques: Expressing, Incubation, Cell Counting, Flow Cytometry, Reverse Transcription, Real-time Polymerase Chain Reaction, Control, Standard Deviation

Overexpression of miR-375 reverses the effects of Dex treatment on the expression levels of apoptosis-related proteins. (A and B) Protein/β-actin expression levels of Bcl-2, Bax and cleaved caspase-3 following Dex treatment and transfection with miR-375 mimic measured using western blot analysis. β-actin was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. *** P<0.001 vs. Control; ^ P<0.05, ^^^ P<0.001 vs. Dex + MC. MC, miR-375 mimic control; M, miR-375 mimic; Dex, dexamethasone.

Journal: International Journal of Molecular Medicine

Article Title: Overexpression of miR-375 reverses the effects of dexamethasone on the viability, migration, invasion and apoptosis of human airway epithelial cells by targeting DUSP6

doi: 10.3892/ijmm.2022.5081

Figure Lengend Snippet: Overexpression of miR-375 reverses the effects of Dex treatment on the expression levels of apoptosis-related proteins. (A and B) Protein/β-actin expression levels of Bcl-2, Bax and cleaved caspase-3 following Dex treatment and transfection with miR-375 mimic measured using western blot analysis. β-actin was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. *** P<0.001 vs. Control; ^ P<0.05, ^^^ P<0.001 vs. Dex + MC. MC, miR-375 mimic control; M, miR-375 mimic; Dex, dexamethasone.

Article Snippet: 9HTE cell apoptosis was detected using flow cytometry with an Annexin V-FITC/propidium iodide (PI) apoptosis kit (A211; GeneBio Systems, Inc.) as per the manufacturer's instructions.

Techniques: Over Expression, Expressing, Transfection, Western Blot, Control, Standard Deviation

Overexpression of DUSP6 reversed the effects of the overexpression of miR-375 on the expression of apoptosis-related proteins in Dex-treated 9HTE cells. (A and B) Protein/β-actin expression levels of Bcl-2, Bax and cleaved caspase-3 following Dex treatment and transfection with miR-375 mimic and DUSP6 overexpression plasmid measured using western blot analysis. β-actin was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. *** P<0.001 vs. control; ^ P<0.05, ^^ P<0.01 and ^^^ P<0.001 vs. Dex + MC + NC; && P<0.01 and &&& P<0.001 vs. Dex + M + NC; ## P<0.01 and ### P<0.001 vs. Dex + MC + DUSP6. NC, negative control; DUSP6, dual specificity phosphatase 6; M, miR-375 mimic; MC, miR-375 mimic control; Dex, dexamethasone.

Journal: International Journal of Molecular Medicine

Article Title: Overexpression of miR-375 reverses the effects of dexamethasone on the viability, migration, invasion and apoptosis of human airway epithelial cells by targeting DUSP6

doi: 10.3892/ijmm.2022.5081

Figure Lengend Snippet: Overexpression of DUSP6 reversed the effects of the overexpression of miR-375 on the expression of apoptosis-related proteins in Dex-treated 9HTE cells. (A and B) Protein/β-actin expression levels of Bcl-2, Bax and cleaved caspase-3 following Dex treatment and transfection with miR-375 mimic and DUSP6 overexpression plasmid measured using western blot analysis. β-actin was employed as an internal control. All experiments were performed in triplicate and experimental data are expressed as the mean ± standard deviation. *** P<0.001 vs. control; ^ P<0.05, ^^ P<0.01 and ^^^ P<0.001 vs. Dex + MC + NC; && P<0.01 and &&& P<0.001 vs. Dex + M + NC; ## P<0.01 and ### P<0.001 vs. Dex + MC + DUSP6. NC, negative control; DUSP6, dual specificity phosphatase 6; M, miR-375 mimic; MC, miR-375 mimic control; Dex, dexamethasone.

Article Snippet: 9HTE cell apoptosis was detected using flow cytometry with an Annexin V-FITC/propidium iodide (PI) apoptosis kit (A211; GeneBio Systems, Inc.) as per the manufacturer's instructions.

Techniques: Over Expression, Expressing, Transfection, Plasmid Preparation, Western Blot, Control, Standard Deviation, Negative Control

CTD induces apoptosis in A549 cells. (A) Flow cytometric analysis of A549 cell apoptosis by double staining with Annexin V-FITC and propidium iodide (PI). (B) The protein expression of Bax, Bcl-2, active caspase-3 were determined by western blotting. The protein expression of GAPDH was as used as the internal control. The protein expressions were quantified for (C) Bcl-2, (D) Bax and (E) active caspase-3. Images were analyzed by Image-Pro Plus 6.0 software. Results are presented as the mean ± standard deviation of three independent experiments. *P<0.05 was considered to indicate a statistically significantly difference vs. NC groups. Bcl-2, B-cell lymphoma-2; Bax, Bcl-associated X; CTD, cantharidin; FITC, fluorescein isothiocyanate; NC, negative control.

Journal: Oncology Letters

Article Title: Cantharidin suppresses cell growth and migration, and activates autophagy in human non-small cell lung cancer cells

doi: 10.3892/ol.2018.8141

Figure Lengend Snippet: CTD induces apoptosis in A549 cells. (A) Flow cytometric analysis of A549 cell apoptosis by double staining with Annexin V-FITC and propidium iodide (PI). (B) The protein expression of Bax, Bcl-2, active caspase-3 were determined by western blotting. The protein expression of GAPDH was as used as the internal control. The protein expressions were quantified for (C) Bcl-2, (D) Bax and (E) active caspase-3. Images were analyzed by Image-Pro Plus 6.0 software. Results are presented as the mean ± standard deviation of three independent experiments. *P<0.05 was considered to indicate a statistically significantly difference vs. NC groups. Bcl-2, B-cell lymphoma-2; Bax, Bcl-associated X; CTD, cantharidin; FITC, fluorescein isothiocyanate; NC, negative control.

Article Snippet: Cell apoptosis analysis An Annexin V-Fluorescein Isothiocyanate (FITC)/propidium iodide (PI) Apoptosis Detection kit (Beijing Chemclin Biotech Co. Ltd., Beijing, China) was used to detect apoptosis according to the manufacturer's protocol.

Techniques: Double Staining, Expressing, Western Blot, Control, Software, Standard Deviation, Negative Control