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super resolution confocal fluorescence microscope Figure 3 A. The MFI was determined by ImageJ software. Bar graphs are presented as mean ± sd, n = 3. (C) The cellular mean fluorescence intensity (MFI) measured by Thermo high-content imaging and screening (HCS) system. HeLa-Cox8-EGFP-actin-mCherry cells were exposed to 1 Gy, 2 Gy, and 4 Gy gamma-ray, respectively. MFI changed with time after the γ-ray irradiation. " width="250" height="auto" />Super Resolution Confocal Fluorescence Microscope, supplied by Evident Corporation, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/result/super resolution confocal fluorescence microscope/product/Evident Corporation Average 95 stars, based on 1 article reviews
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highresolution laser confocal fluorescence microscope lcms Figure 3 A. The MFI was determined by ImageJ software. Bar graphs are presented as mean ± sd, n = 3. (C) The cellular mean fluorescence intensity (MFI) measured by Thermo high-content imaging and screening (HCS) system. HeLa-Cox8-EGFP-actin-mCherry cells were exposed to 1 Gy, 2 Gy, and 4 Gy gamma-ray, respectively. MFI changed with time after the γ-ray irradiation. " width="250" height="auto" />Highresolution Laser Confocal Fluorescence Microscope Lcms, supplied by Evident Corporation, 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/highresolution laser confocal fluorescence microscope lcms/product/Evident Corporation Average 99 stars, based on 1 article reviews
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fluorescence microscope Figure 3 A. The MFI was determined by ImageJ software. Bar graphs are presented as mean ± sd, n = 3. (C) The cellular mean fluorescence intensity (MFI) measured by Thermo high-content imaging and screening (HCS) system. HeLa-Cox8-EGFP-actin-mCherry cells were exposed to 1 Gy, 2 Gy, and 4 Gy gamma-ray, respectively. MFI changed with time after the γ-ray irradiation. " width="250" height="auto" />Fluorescence Microscope, supplied by Evident Corporation, 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/fluorescence microscope/product/Evident Corporation Average 99 stars, based on 1 article reviews
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fluorescence and confocal microscopes leitz aristoplan Figure 3 A. The MFI was determined by ImageJ software. Bar graphs are presented as mean ± sd, n = 3. (C) The cellular mean fluorescence intensity (MFI) measured by Thermo high-content imaging and screening (HCS) system. HeLa-Cox8-EGFP-actin-mCherry cells were exposed to 1 Gy, 2 Gy, and 4 Gy gamma-ray, respectively. MFI changed with time after the γ-ray irradiation. " width="250" height="auto" />Fluorescence And Confocal Microscopes Leitz Aristoplan, supplied by Leitz GmbH, 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/fluorescence and confocal microscopes leitz aristoplan/product/Leitz GmbH Average 90 stars, based on 1 article reviews
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spinning disk confocal microscope opera Figure 3 A. The MFI was determined by ImageJ software. Bar graphs are presented as mean ± sd, n = 3. (C) The cellular mean fluorescence intensity (MFI) measured by Thermo high-content imaging and screening (HCS) system. HeLa-Cox8-EGFP-actin-mCherry cells were exposed to 1 Gy, 2 Gy, and 4 Gy gamma-ray, respectively. MFI changed with time after the γ-ray irradiation. " width="250" height="auto" />Spinning Disk Confocal Microscope Opera, supplied by Evotec 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/spinning disk confocal microscope opera/product/Evotec Inc Average 90 stars, based on 1 article reviews
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hyperspectral confocal fluorescence imaging system Figure 3 A. The MFI was determined by ImageJ software. Bar graphs are presented as mean ± sd, n = 3. (C) The cellular mean fluorescence intensity (MFI) measured by Thermo high-content imaging and screening (HCS) system. HeLa-Cox8-EGFP-actin-mCherry cells were exposed to 1 Gy, 2 Gy, and 4 Gy gamma-ray, respectively. MFI changed with time after the γ-ray irradiation. " width="250" height="auto" />Hyperspectral Confocal Fluorescence Imaging System, supplied by Sandia National Laboratories, 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/hyperspectral confocal fluorescence imaging system/product/Sandia National Laboratories Average 90 stars, based on 1 article reviews
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Image Search Results
Figure 3 A. The MFI was determined by ImageJ software. Bar graphs are presented as mean ± sd, n = 3. (C) The cellular mean fluorescence intensity (MFI) measured by Thermo high-content imaging and screening (HCS) system. HeLa-Cox8-EGFP-actin-mCherry cells were exposed to 1 Gy, 2 Gy, and 4 Gy gamma-ray, respectively. MFI changed with time after the γ-ray irradiation. " width="100%" height="100%">
Journal: iScience
Article Title: In situ observation of mitochondrial biogenesis as the early event of apoptosis
doi: 10.1016/j.isci.2021.103038
Figure Lengend Snippet: In situ observation of the biological effects of gamma-radiation via the dual fluorescence reporter system (A) HeLa-cox8-EGFP-actin-mCherry cells were exposed to 1 Gy, 2 Gy, 4 Gy gamma-ray and incubated for 24 hr and observed with confocal laser scanning microscope. Green color indicates the mitochondria encoding COX8-EGFP, red color shows the actin encoded by actin-mCherry, and blue color represents the DAPI-stained nuclei. Scale bar: 5 μm. (B) The ratio comparison for the mean fluorescence intensity (MFI) of GFP over mCherry fluorescence intensities quantified in the
Article Snippet: Radiation experiments were performed after 24 h of incubation to observe cellular mitochondrial morphology at 6 h and 24 h, respectively, using a
Techniques: In Situ, Fluorescence, Incubation, Laser-Scanning Microscopy, Staining, Software, Imaging, Irradiation