software version r 2014a Search Results


e-prime  (Psychology Software Tools)
99
Psychology Software Tools e-prime
E Prime, supplied by Psychology Software Tools, 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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e-prime - by Bioz Stars, 2026-06
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version 2014a  (MathWorks Inc)
98
MathWorks Inc version 2014a
Version 2014a, supplied by MathWorks Inc, 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/result/version 2014a/product/MathWorks Inc
Average 98 stars, based on 1 article reviews
version 2014a - by Bioz Stars, 2026-06
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r software package rdrobust  (STATA Corporation)
99
STATA Corporation r software package rdrobust
R Software Package Rdrobust, supplied by STATA Corporation, 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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Average 99 stars, based on 1 article reviews
r software package rdrobust - by Bioz Stars, 2026-06
99/100 stars
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incucyte zoom software  (Sartorius AG)
99
Sartorius AG incucyte zoom software
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Incucyte Zoom 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
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Average 99 stars, based on 1 article reviews
incucyte zoom software - by Bioz Stars, 2026-06
99/100 stars
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xlstat 2014 software  (Addinsoft inc)
90
Addinsoft inc xlstat 2014 software
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Xlstat 2014 Software, supplied by Addinsoft 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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Average 90 stars, based on 1 article reviews
xlstat 2014 software - by Bioz Stars, 2026-06
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sas version 9.3  (SAS institute)
90
SAS institute sas version 9.3
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Sas Version 9.3, supplied by SAS institute, 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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sas version 9.3 - by Bioz Stars, 2026-06
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stereo investigator software version 9.14.5 32-bit  (MBF Bioscience)
90
MBF Bioscience stereo investigator software version 9.14.5 32-bit
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Stereo Investigator Software Version 9.14.5 32 Bit, supplied by MBF Bioscience, 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/stereo investigator software version 9.14.5 32-bit/product/MBF Bioscience
Average 90 stars, based on 1 article reviews
stereo investigator software version 9.14.5 32-bit - by Bioz Stars, 2026-06
90/100 stars
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social statistics windows, version 24.0  (SPSS Inc)
90
SPSS Inc social statistics windows, version 24.0
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Social Statistics Windows, Version 24.0, supplied by SPSS 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/social statistics windows, version 24.0/product/SPSS Inc
Average 90 stars, based on 1 article reviews
social statistics windows, version 24.0 - by Bioz Stars, 2026-06
90/100 stars
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cirrus oct  (Carl Zeiss)
90
Carl Zeiss cirrus oct
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Cirrus Oct, supplied by Carl Zeiss, 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/cirrus oct/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
cirrus oct - by Bioz Stars, 2026-06
90/100 stars
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prism version 5  (GraphPad Software Inc)
90
GraphPad Software Inc prism version 5
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Prism Version 5, 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
https://www.bioz.com/result/prism version 5/product/GraphPad Software Inc
Average 90 stars, based on 1 article reviews
prism version 5 - by Bioz Stars, 2026-06
90/100 stars
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comsol multiphysics 5.3a  (COMSOL Inc)
90
COMSOL Inc comsol multiphysics 5.3a
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Comsol Multiphysics 5.3a, supplied by COMSOL 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/comsol multiphysics 5.3a/product/COMSOL Inc
Average 90 stars, based on 1 article reviews
comsol multiphysics 5.3a - by Bioz Stars, 2026-06
90/100 stars
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runtime version 8 3  (MathWorks Inc)
96
MathWorks Inc runtime version 8 3
Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in <t>Incucyte</t> ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).
Runtime Version 8 3, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/runtime version 8 3/product/MathWorks Inc
Average 96 stars, based on 1 article reviews
runtime version 8 3 - by Bioz Stars, 2026-06
96/100 stars
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Image Search Results


Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in Incucyte ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).

Journal: Cancers

Article Title: DNA Replication Licensing Protein MCM10 Promotes Tumor Progression and Is a Novel Prognostic Biomarker and Potential Therapeutic Target in Breast Cancer

doi: 10.3390/cancers10090282

Figure Lengend Snippet: Cancer hallmarks of stable MCM10 knockdown (KD) in MCF 7 cells. ( A , B ) relative expression of MCM10 in stable MCM10-KD MCF 7 cell lines assessed by qPCR and Western blots ( n = 3, *** p < 0.001); ( C ) apoptosis analysis by Annexin V/Propidium Iodide flow cytometry showed no difference between stable MCM10-control MCF7 cell lines and stable MCM10-KD MCF 7 cell lines ( n = 3, * p < 0.05); ( D ) following MCM10 KD, the MCM10-KD MCF7 cells showed a decrease in cell proliferation monitored for seven days using phase contrast images in Incucyte ZOOM analysis software ( n = 6); ( E ) MTT assay using stable cells showed a similar observation indicating decreased proliferation in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( F ) analysis cell cycle markers by western blot and QPCR showed a decrease in cycling D1 expression indicating impaired cell proliferation in in MCM10-KD MCF 7 cells ( n = 3, * p < 0.05); ( G ) wound healing migration assay performed by using Incucyte ZOOM showed a decrease in cell migration in MCM10-KD MCF 7 cell lines. Wound heal quantified by relative Gap size using Incucyte ZOOM software ( n = 6, * p < 0.05); ( H ) Transwell cell migration assay was used to confirm our observation and showed a similar decrease in the number of migrating cells in MCM10-KD MCF 7 cells ( n = 3, ** p < 0.01); ( I ) colony formation assay performed using soft agar showed a decrease in the number of colonies in MCM10-KD MCF 7 cells compared to the control cells. ( n = 3, * p < 0.05).

Article Snippet: Data were analyzed using the IncuCyte Zoom software (version 2014a Essen Bioscience, Ann Arbor, MI, USA), which quantified cell surface area coverage as confluence values.

Techniques: Expressing, Western Blot, Flow Cytometry, Software, MTT Assay, Migration, Cell Migration Assay, Colony Assay