tm version 2016b Search Results


incucyte tm software  (Sartorius AG)
99
Sartorius AG incucyte tm software
a Effect of various doses of AOAA on the proliferation efficiency of HDLECs after 24 h ( n = 5). Proliferation was determined by using <t>IncuCyte</t> Zoom. b Quantification of flow cytometrically detected Annexin V-positive cells 24 h after treatment with the indicated concentrations of AOAA and representative flow cytometry images ( n = 5). c AOAA treatment of HDLECs slowed wound closure compared to control cells in wound healing assay ( n = 4). d Effect of 1 mM and 4 mM AOAA treatment on HDLECs on tube formation. Evaluation was performed after 4 h and 24 h ( n = 5). Data are presented as means ± SEM. Statistical significance was analyzed with ( a , b ) one-way ANOVA and Dunnett’s multiple comparison test or ( c , d ) two-way ANOVA and Tukey’s multiple comparison test. * p < 0.05, ** p < 0.01; *** p < 0.001; **** p < 0.0001.
Incucyte Tm Software, supplied by Sartorius AG, 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/result/incucyte tm software/product/Sartorius AG
Average 99 stars, based on 1 article reviews
incucyte tm software - by Bioz Stars, 2026-03
99/100 stars
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tm version 2016b  (MathWorks Inc)
90
MathWorks Inc tm version 2016b
a Effect of various doses of AOAA on the proliferation efficiency of HDLECs after 24 h ( n = 5). Proliferation was determined by using <t>IncuCyte</t> Zoom. b Quantification of flow cytometrically detected Annexin V-positive cells 24 h after treatment with the indicated concentrations of AOAA and representative flow cytometry images ( n = 5). c AOAA treatment of HDLECs slowed wound closure compared to control cells in wound healing assay ( n = 4). d Effect of 1 mM and 4 mM AOAA treatment on HDLECs on tube formation. Evaluation was performed after 4 h and 24 h ( n = 5). Data are presented as means ± SEM. Statistical significance was analyzed with ( a , b ) one-way ANOVA and Dunnett’s multiple comparison test or ( c , d ) two-way ANOVA and Tukey’s multiple comparison test. * p < 0.05, ** p < 0.01; *** p < 0.001; **** p < 0.0001.
Tm Version 2016b, supplied by MathWorks Inc, 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/result/tm version 2016b/product/MathWorks Inc
Average 90 stars, based on 1 article reviews
tm version 2016b - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
thermo-calc tm software  (Thermo Fisher)
90
Thermo Fisher thermo-calc tm software
a Effect of various doses of AOAA on the proliferation efficiency of HDLECs after 24 h ( n = 5). Proliferation was determined by using <t>IncuCyte</t> Zoom. b Quantification of flow cytometrically detected Annexin V-positive cells 24 h after treatment with the indicated concentrations of AOAA and representative flow cytometry images ( n = 5). c AOAA treatment of HDLECs slowed wound closure compared to control cells in wound healing assay ( n = 4). d Effect of 1 mM and 4 mM AOAA treatment on HDLECs on tube formation. Evaluation was performed after 4 h and 24 h ( n = 5). Data are presented as means ± SEM. Statistical significance was analyzed with ( a , b ) one-way ANOVA and Dunnett’s multiple comparison test or ( c , d ) two-way ANOVA and Tukey’s multiple comparison test. * p < 0.05, ** p < 0.01; *** p < 0.001; **** p < 0.0001.
Thermo Calc Tm Software, supplied by Thermo Fisher, 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/result/thermo-calc tm software/product/Thermo Fisher
Average 90 stars, based on 1 article reviews
thermo-calc tm software - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


a Effect of various doses of AOAA on the proliferation efficiency of HDLECs after 24 h ( n = 5). Proliferation was determined by using IncuCyte Zoom. b Quantification of flow cytometrically detected Annexin V-positive cells 24 h after treatment with the indicated concentrations of AOAA and representative flow cytometry images ( n = 5). c AOAA treatment of HDLECs slowed wound closure compared to control cells in wound healing assay ( n = 4). d Effect of 1 mM and 4 mM AOAA treatment on HDLECs on tube formation. Evaluation was performed after 4 h and 24 h ( n = 5). Data are presented as means ± SEM. Statistical significance was analyzed with ( a , b ) one-way ANOVA and Dunnett’s multiple comparison test or ( c , d ) two-way ANOVA and Tukey’s multiple comparison test. * p < 0.05, ** p < 0.01; *** p < 0.001; **** p < 0.0001.

Journal: Communications Biology

Article Title: Cystathionine β-synthase as novel endogenous regulator of lymphangiogenesis via modulating VEGF receptor 2 and 3

doi: 10.1038/s42003-022-03923-7

Figure Lengend Snippet: a Effect of various doses of AOAA on the proliferation efficiency of HDLECs after 24 h ( n = 5). Proliferation was determined by using IncuCyte Zoom. b Quantification of flow cytometrically detected Annexin V-positive cells 24 h after treatment with the indicated concentrations of AOAA and representative flow cytometry images ( n = 5). c AOAA treatment of HDLECs slowed wound closure compared to control cells in wound healing assay ( n = 4). d Effect of 1 mM and 4 mM AOAA treatment on HDLECs on tube formation. Evaluation was performed after 4 h and 24 h ( n = 5). Data are presented as means ± SEM. Statistical significance was analyzed with ( a , b ) one-way ANOVA and Dunnett’s multiple comparison test or ( c , d ) two-way ANOVA and Tukey’s multiple comparison test. * p < 0.05, ** p < 0.01; *** p < 0.001; **** p < 0.0001.

Article Snippet: For statistical analysis, the fold increase in density within 24 h was calculated using the IncuCyte TM software (Version 2016B and 2018A, Essen Biosciences, Hertfordshire, UK).

Techniques: Flow Cytometry, Control, Wound Healing Assay, Comparison

a Efficiency of CBS knockdown determined qRT-PCR 72 h post-transfection. Reduced expression of CBS in HDLECs after 72 h transfected with either siR_CBS-5, siR_CBS-6, or negative control (NC) siRNA ( n = 21). b Quantification of immunofluorescence staining of HDLECs transfected with either siR_CBS-5, siR_CBS-6, or negative control (NC) siRNA stained for CBS ( n = 3). c Effect of CBS silencing on HDLECs proliferation transfected with either siR_CBS-5 or siR_CBS-6 compared with NC siRNA transfected cells. Proliferation was determined 72 h after transfection by using IncuCyte Zoom ( n = 5). d Quantification of flow cytometrically detected Annexin V-positive HDLECs 72 h after transfection with either siR_CBS-5, siR_CBS-6, or negative control (NC) siRNA ( n = 5). e Wound healing assay with negative control (NC) siRNA, siR_CBS-5 or siR_CBS-6 siRNA treated HDLECs after 72 h transfection ( n = 6). f Tube formation assay after 72 h transfection of HDLECs transfected with either negative control (NC) siRNA, siR_CBS-5 or siR_CBS-6 siRNA. Evaluation was performed after 4 h and 24 h ( n = 4). Data are presented as means ± SEM. Statistical significance was analyzed with ( a – d ) one-way ANOVA and Dunnett’s multiple comparison test or ( e , f ) two-way ANOVA and Tukey’s multiple comparison test. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

Journal: Communications Biology

Article Title: Cystathionine β-synthase as novel endogenous regulator of lymphangiogenesis via modulating VEGF receptor 2 and 3

doi: 10.1038/s42003-022-03923-7

Figure Lengend Snippet: a Efficiency of CBS knockdown determined qRT-PCR 72 h post-transfection. Reduced expression of CBS in HDLECs after 72 h transfected with either siR_CBS-5, siR_CBS-6, or negative control (NC) siRNA ( n = 21). b Quantification of immunofluorescence staining of HDLECs transfected with either siR_CBS-5, siR_CBS-6, or negative control (NC) siRNA stained for CBS ( n = 3). c Effect of CBS silencing on HDLECs proliferation transfected with either siR_CBS-5 or siR_CBS-6 compared with NC siRNA transfected cells. Proliferation was determined 72 h after transfection by using IncuCyte Zoom ( n = 5). d Quantification of flow cytometrically detected Annexin V-positive HDLECs 72 h after transfection with either siR_CBS-5, siR_CBS-6, or negative control (NC) siRNA ( n = 5). e Wound healing assay with negative control (NC) siRNA, siR_CBS-5 or siR_CBS-6 siRNA treated HDLECs after 72 h transfection ( n = 6). f Tube formation assay after 72 h transfection of HDLECs transfected with either negative control (NC) siRNA, siR_CBS-5 or siR_CBS-6 siRNA. Evaluation was performed after 4 h and 24 h ( n = 4). Data are presented as means ± SEM. Statistical significance was analyzed with ( a – d ) one-way ANOVA and Dunnett’s multiple comparison test or ( e , f ) two-way ANOVA and Tukey’s multiple comparison test. * p < 0.05; ** p < 0.01; *** p < 0.001; **** p < 0.0001.

Article Snippet: For statistical analysis, the fold increase in density within 24 h was calculated using the IncuCyte TM software (Version 2016B and 2018A, Essen Biosciences, Hertfordshire, UK).

Techniques: Knockdown, Quantitative RT-PCR, Transfection, Expressing, Negative Control, Immunofluorescence, Staining, Wound Healing Assay, Tube Formation Assay, Comparison