spinning disc confocal microscope nikon eclipse te2000-e Search Results


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
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te2000 e inverted confocal microscope - by Bioz Stars, 2026-03
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te2000e spinning disc confocal microscope  (Nikon)
90
Nikon te2000e spinning disc 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.
Te2000e Spinning Disc Confocal 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/te2000e spinning disc confocal microscope/product/Nikon
Average 90 stars, based on 1 article reviews
te2000e spinning disc confocal microscope - by Bioz Stars, 2026-03
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spinning disk confocal nikon te2000e2 inverted microscope  (Nikon)
90
Nikon spinning disk confocal nikon te2000e2 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.
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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Average 90 stars, based on 1 article reviews
spinning disk confocal nikon te2000e2 inverted microscope - by Bioz Stars, 2026-03
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eclipse te2000 e microscope  (Nikon)
99
Nikon eclipse te2000 e 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.
Eclipse Te2000 E 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/eclipse te2000 e microscope/product/Nikon
Average 99 stars, based on 1 article reviews
eclipse te2000 e microscope - by Bioz Stars, 2026-03
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te2000-e spinning disk confocal microscope  (Nikon)
90
Nikon te2000-e spinning disk 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 Spinning Disk Confocal 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/te2000-e spinning disk confocal microscope/product/Nikon
Average 90 stars, based on 1 article reviews
te2000-e spinning disk confocal microscope - by Bioz Stars, 2026-03
90/100 stars
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volocity spinning disk confocal microscope nikon te 2000-e  (Nikon)
90
Nikon volocity spinning disk confocal microscope nikon te 2000-e
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.
Volocity Spinning Disk Confocal Microscope Nikon 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
https://www.bioz.com/result/volocity spinning disk confocal microscope nikon te 2000-e/product/Nikon
Average 90 stars, based on 1 article reviews
volocity spinning disk confocal microscope nikon te 2000-e - by Bioz Stars, 2026-03
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eclipse te 2000-e inverted spinning disk confocal microscope  (Nikon)
90
Nikon eclipse te 2000-e inverted spinning disk 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.
Eclipse Te 2000 E Inverted Spinning Disk Confocal 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/eclipse te 2000-e inverted spinning disk confocal microscope/product/Nikon
Average 90 stars, based on 1 article reviews
eclipse te 2000-e inverted spinning disk confocal microscope - by Bioz Stars, 2026-03
90/100 stars
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spinning disc confocal microscope nikon eclipse te2000-e  (Nikon)
90
Nikon spinning disc confocal microscope nikon eclipse te2000-e
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.
Spinning Disc Confocal 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
https://www.bioz.com/result/spinning disc confocal microscope nikon eclipse te2000-e/product/Nikon
Average 90 stars, based on 1 article reviews
spinning disc confocal microscope nikon eclipse te2000-e - by Bioz Stars, 2026-03
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imageem x2 camera  (Hamamatsu)
90
Hamamatsu imageem x2 camera
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.
Imageem X2 Camera, supplied by Hamamatsu, 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
imageem x2 camera - by Bioz Stars, 2026-03
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spinning-disk confocal microscopy nikon eclipse te2000-e  (Nikon)
90
Nikon spinning-disk confocal microscopy nikon eclipse te2000-e
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.
Spinning Disk Confocal Microscopy 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
https://www.bioz.com/result/spinning-disk confocal microscopy nikon eclipse te2000-e/product/Nikon
Average 90 stars, based on 1 article reviews
spinning-disk confocal microscopy nikon eclipse te2000-e - by Bioz Stars, 2026-03
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te2000-e inverted microscope  (Nikon)
90
Nikon 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.
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/te2000-e inverted microscope/product/Nikon
Average 90 stars, based on 1 article reviews
te2000-e inverted microscope - by Bioz Stars, 2026-03
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metamorph software  (MetaMorph Inc)
90
MetaMorph Inc metamorph software
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.
Metamorph Software, supplied by MetaMorph 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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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