axiovert imaging software Search Results


90
Carl Zeiss axiovert v4.8 software
Axiovert V4.8 Software, 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
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96
Carl Zeiss axiovert 200m
Axiovert 200m, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Carl Zeiss axiovert imaging software
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Axiovert Imaging Software, 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
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Average 90 stars, based on 1 article reviews
axiovert imaging software - by Bioz Stars, 2026-05
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90
universal imaging inc metamorph 4.5.6 software
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Metamorph 4.5.6 Software, supplied by universal imaging 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
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Carl Zeiss camera zeiss axiocam hr
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Camera Zeiss Axiocam Hr, 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
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90
Carl Zeiss axiovert2 imaging software
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Axiovert2 Imaging Software, 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/axiovert2 imaging software/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
axiovert2 imaging software - by Bioz Stars, 2026-05
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96
Carl Zeiss axiovision 4 5 image acquisition software
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Axiovision 4 5 Image Acquisition Software, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Carl Zeiss lsm 5 pascal (v 3.2 sp2) software
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Lsm 5 Pascal (V 3.2 Sp2) Software, 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
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Average 90 stars, based on 1 article reviews
lsm 5 pascal (v 3.2 sp2) software - by Bioz Stars, 2026-05
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90
Carl Zeiss axiocam/axiovision software
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Axiocam/Axiovision Software, 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
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Average 90 stars, based on 1 article reviews
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Carl Zeiss axiovert laser 100m confocal microscope
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Axiovert Laser 100m Confocal Microscope, 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
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96
Carl Zeiss apotome module
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Apotome Module, supplied by Carl Zeiss, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Carl Zeiss inverted microscope
(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) <t>Representative</t> <t>MCA</t> formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss <t>Axiovert</t> Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.
Inverted Microscope, 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
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Average 90 stars, based on 1 article reviews
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Image Search Results


(A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) Representative MCA formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss Axiovert Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.

Journal:

Article Title: Ovarian Cancer Cell Detachment and Multicellular Aggregate Formation Are Regulated by MT1-MMP: A Potential Role in Intra-Peritoneal Metastatic Dissemination

doi: 10.1158/0008-5472.CAN-08-4151

Figure Lengend Snippet: (A) Expression of MT1-MMP RNA in DOV13 MCAs or 2D cultures. Real time RT-PCR was performed to detect RNA expression. Shown is the average of three independent experiments ± standard deviation. (*p<.05). (B) Expression of MT1-MMP protein. Western blot was performed to detect relative MT1-MMP protein levels with β-tubulin as a loading control. Arrow - 55 kDa active MT1-MMP; arrowhead - 43 kDa MT1-MMP autolysis product. (C) Representative MCA formed by OVCA 433 or DOV13 cells. (D) Expression of MT1-MMP augments MCA formation. Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss Axiovert Imaging Software. Data shown are expressed in μm, and represent the mean diameter measurement of n=10 MCAs. (+) indicates p<.05 relative to vector-transfected cells; (*) indicates p<.05 relative to cells expressing wild type MT1-MMP. Untransfected DOV13 cells, that express similar levels of endogenous MT1-MMP, are shown for comparison.

Article Snippet: Cells were cultured for MCA formation using the hanging drop method and measured using a Zeiss Axiovert Imaging Software.

Techniques: Expressing, Quantitative RT-PCR, RNA Expression, Standard Deviation, Western Blot, Cell Culture, Imaging, Software, Plasmid Preparation, Transfection