confocal inverted microscope nikon eclipse te2000-e Search Results


eclipse te2000 e confocal microscope  (Nikon)
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Nikon eclipse te2000 e confocal microscope
Eclipse Te2000 E Confocal Microscope, supplied by Nikon, 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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confocal laser scanning microscope digital eclipse te 2000-e  (Nikon)
90
Nikon confocal laser scanning microscope digital eclipse te 2000-e
Confocal Laser Scanning Microscope Digital Eclipse Te 2000 E, supplied by Nikon, 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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te2000 e inverted confocal microscope  (Nikon)
99
Nikon te2000 e inverted confocal microscope
Huh7 cells were infected with HCV (strain Jc1) using 30 TCID 50 /cell and 48 h later cells were fixed and processed for fluorescence microscopy. In case of samples shown in panels B–D, cells were first transfected with expression constructs specified in the left of each panel and 24 h later cells were infected as described above. Samples were analyzed with a Nikon <t>TE2000-E</t> inverted confocal microscope at 60× magnification. (A)–(D) Colocalization of HCV proteins specified in the top of each panel with protein disulphide isomerase (PDI; an ER marker), GFP-Rab21 (marker for early endosomes), GFP-Rab7 (marker for late endosomes) or βCOP-YFP (marker for COP I vesicles). The upper panels represent a low magnification overview; boxed areas are shown as enlargement in the corresponding panel below. The nucleus was stained with DAPI (blue). Scale bars represent 10 µm (top panels) and 2 µm (lower panels). The quantification of the degree of colocalization (Pearson's correlation coefficient) is given at the top of the enlarged pictures.
Te2000 E Inverted Confocal Microscope, supplied by Nikon, 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/te2000 e inverted confocal microscope/product/Nikon
Average 99 stars, based on 1 article reviews
te2000 e inverted confocal microscope - by Bioz Stars, 2026-02
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confocal microscopy nikon eclipse te2000-e inverted microscope  (Nikon)
90
Nikon confocal microscopy nikon eclipse te2000-e inverted microscope
Huh7 cells were infected with HCV (strain Jc1) using 30 TCID 50 /cell and 48 h later cells were fixed and processed for fluorescence microscopy. In case of samples shown in panels B–D, cells were first transfected with expression constructs specified in the left of each panel and 24 h later cells were infected as described above. Samples were analyzed with a Nikon <t>TE2000-E</t> inverted confocal microscope at 60× magnification. (A)–(D) Colocalization of HCV proteins specified in the top of each panel with protein disulphide isomerase (PDI; an ER marker), GFP-Rab21 (marker for early endosomes), GFP-Rab7 (marker for late endosomes) or βCOP-YFP (marker for COP I vesicles). The upper panels represent a low magnification overview; boxed areas are shown as enlargement in the corresponding panel below. The nucleus was stained with DAPI (blue). Scale bars represent 10 µm (top panels) and 2 µm (lower panels). The quantification of the degree of colocalization (Pearson's correlation coefficient) is given at the top of the enlarged pictures.
Confocal Microscopy Nikon Eclipse Te2000 E Inverted Microscope, supplied by Nikon, 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/confocal microscopy nikon eclipse te2000-e inverted microscope/product/Nikon
Average 90 stars, based on 1 article reviews
confocal microscopy nikon eclipse te2000-e inverted microscope - by Bioz Stars, 2026-02
90/100 stars
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confocal microscopy  (Nikon)
90
Nikon confocal microscopy
Huh7 cells were infected with HCV (strain Jc1) using 30 TCID 50 /cell and 48 h later cells were fixed and processed for fluorescence microscopy. In case of samples shown in panels B–D, cells were first transfected with expression constructs specified in the left of each panel and 24 h later cells were infected as described above. Samples were analyzed with a Nikon <t>TE2000-E</t> inverted confocal microscope at 60× magnification. (A)–(D) Colocalization of HCV proteins specified in the top of each panel with protein disulphide isomerase (PDI; an ER marker), GFP-Rab21 (marker for early endosomes), GFP-Rab7 (marker for late endosomes) or βCOP-YFP (marker for COP I vesicles). The upper panels represent a low magnification overview; boxed areas are shown as enlargement in the corresponding panel below. The nucleus was stained with DAPI (blue). Scale bars represent 10 µm (top panels) and 2 µm (lower panels). The quantification of the degree of colocalization (Pearson's correlation coefficient) is given at the top of the enlarged pictures.
Confocal Microscopy, supplied by Nikon, 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/confocal microscopy/product/Nikon
Average 90 stars, based on 1 article reviews
confocal microscopy - by Bioz Stars, 2026-02
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confocal laser scanning microscope (clsm) nikon eclipse te2000-e  (Nikon)
90
Nikon confocal laser scanning microscope (clsm) nikon eclipse te2000-e
<t>Confocal</t> <t>microscopy</t> images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.
Confocal Laser Scanning Microscope (Clsm) Nikon Eclipse Te2000 E, supplied by Nikon, 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
confocal laser scanning microscope (clsm) nikon eclipse te2000-e - by Bioz Stars, 2026-02
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c1si spectral imaging confocal laser scanning system  (Nikon)
99
Nikon c1si spectral imaging confocal laser scanning system
<t>Confocal</t> <t>microscopy</t> images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.
C1si Spectral Imaging Confocal Laser Scanning System, supplied by Nikon, 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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fv1000 fcs confocal laser scanning microscope  (Evident Corporation)
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Evident Corporation fv1000 fcs confocal laser scanning microscope
<t>Confocal</t> <t>microscopy</t> images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.
Fv1000 Fcs Confocal Laser Scanning Microscope, supplied by Evident Corporation, 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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spinning disk confocal nikon te2000e2 inverted microscope  (Nikon)
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Nikon spinning disk confocal nikon te2000e2 inverted microscope
<t>Confocal</t> <t>microscopy</t> images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.
Spinning Disk Confocal Nikon Te2000e2 Inverted Microscope, supplied by Nikon, 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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ze-1-c1 3.70 digital camera system  (Nikon)
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Nikon ze-1-c1 3.70 digital camera system
<t>Confocal</t> <t>microscopy</t> images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.
Ze 1 C1 3.70 Digital Camera System, supplied by Nikon, 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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confocal fluorescence microscope nikon eclipse te2000-e  (Nikon)
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Nikon confocal fluorescence microscope nikon eclipse te2000-e
<t>Confocal</t> <t>microscopy</t> images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.
Confocal Fluorescence Microscope Nikon Eclipse Te2000 E, supplied by Nikon, 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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confocal microscopy nikon te2000-e  (Nikon)
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Nikon confocal microscopy nikon te2000-e
<t>Confocal</t> <t>microscopy</t> images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.
Confocal Microscopy Nikon Te2000 E, supplied by Nikon, 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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Image Search Results


Huh7 cells were infected with HCV (strain Jc1) using 30 TCID 50 /cell and 48 h later cells were fixed and processed for fluorescence microscopy. In case of samples shown in panels B–D, cells were first transfected with expression constructs specified in the left of each panel and 24 h later cells were infected as described above. Samples were analyzed with a Nikon TE2000-E inverted confocal microscope at 60× magnification. (A)–(D) Colocalization of HCV proteins specified in the top of each panel with protein disulphide isomerase (PDI; an ER marker), GFP-Rab21 (marker for early endosomes), GFP-Rab7 (marker for late endosomes) or βCOP-YFP (marker for COP I vesicles). The upper panels represent a low magnification overview; boxed areas are shown as enlargement in the corresponding panel below. The nucleus was stained with DAPI (blue). Scale bars represent 10 µm (top panels) and 2 µm (lower panels). The quantification of the degree of colocalization (Pearson's correlation coefficient) is given at the top of the enlarged pictures.

Journal: PLoS Pathogens

Article Title: Three-Dimensional Architecture and Biogenesis of Membrane Structures Associated with Hepatitis C Virus Replication

doi: 10.1371/journal.ppat.1003056

Figure Lengend Snippet: Huh7 cells were infected with HCV (strain Jc1) using 30 TCID 50 /cell and 48 h later cells were fixed and processed for fluorescence microscopy. In case of samples shown in panels B–D, cells were first transfected with expression constructs specified in the left of each panel and 24 h later cells were infected as described above. Samples were analyzed with a Nikon TE2000-E inverted confocal microscope at 60× magnification. (A)–(D) Colocalization of HCV proteins specified in the top of each panel with protein disulphide isomerase (PDI; an ER marker), GFP-Rab21 (marker for early endosomes), GFP-Rab7 (marker for late endosomes) or βCOP-YFP (marker for COP I vesicles). The upper panels represent a low magnification overview; boxed areas are shown as enlargement in the corresponding panel below. The nucleus was stained with DAPI (blue). Scale bars represent 10 µm (top panels) and 2 µm (lower panels). The quantification of the degree of colocalization (Pearson's correlation coefficient) is given at the top of the enlarged pictures.

Article Snippet: For image analysis we used a Perkin Elmer Ultraview ERS spinning disk on a Nikon TE2000-E inverted confocal microscope equipped with a Plan-Apochromat VC 60× objective (NA 1.20) and the Volocity 5.3 software package.

Techniques: Infection, Fluorescence, Microscopy, Transfection, Expressing, Construct, Marker, Staining

Confocal microscopy images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.

Journal: Scientific Reports

Article Title: Simultaneous Monitoring of Cell-surface Receptor and Tumor-targeted Photodynamic Therapy via TdT-initiated Poly-G-Quadruplexes

doi: 10.1038/s41598-018-23902-5

Figure Lengend Snippet: Confocal microscopy images of incubated with poly-G-quadruplexes-ThT probe treated A549 ( a ) and HepG2 ( b ). Scale bar: 20 µm. ( c ) The normalized fluorescence intensity of individual cells was quantified from ( a ) and ( b ). Error bars indicate SD, n = 5. **P < 0.01. ( d ) Flow cytometry analysis of Cy5 labeled aptamer-primer with A549 and HepG2 cells, respectively.

Article Snippet: Live cell imaging was performed under confocal laser scanning microscope (CLSM) (Nikon, Eclipse TE2000-E) with a 60× oil immersion objective (Olympus, Melville, NY).

Techniques: Confocal Microscopy, Incubation, Fluorescence, Flow Cytometry, Labeling