olympus cellsens program Search Results


99
Oxford Instruments excel fiji imagej
Excel Fiji Imagej, supplied by Oxford Instruments, 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/product/olympus+cellsens+program/pm35721464-316-0-8?v=Oxford+Instruments
Average 99 stars, based on 1 article reviews
excel fiji imagej - by Bioz Stars, 2026-07
99/100 stars
  Buy from Supplier

99
Olympus cellsens software
Cellsens Software, supplied by Olympus, 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/product/olympus+cellsens+program/pmc09372013-86-18-21?v=Olympus
Average 99 stars, based on 1 article reviews
cellsens software - by Bioz Stars, 2026-07
99/100 stars
  Buy from Supplier

95
Olympus lv200 luminescent microscope
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Lv200 Luminescent Microscope, supplied by Olympus, 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/product/olympus+cellsens+program/pmc09050736-307-6-9?v=Olympus
Average 95 stars, based on 1 article reviews
lv200 luminescent microscope - by Bioz Stars, 2026-07
95/100 stars
  Buy from Supplier

96
Olympus szx16 whole specimen microscope
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Szx16 Whole Specimen Microscope, supplied by Olympus, 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/product/olympus+cellsens+program/pm41594544-66-26-33?v=Olympus
Average 96 stars, based on 1 article reviews
szx16 whole specimen microscope - by Bioz Stars, 2026-07
96/100 stars
  Buy from Supplier

98
Olympus digital camera olympus dp74
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Digital Camera Olympus Dp74, supplied by Olympus, 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/product/olympus+cellsens+program/pmc11582168-119-37-39?v=Olympus
Average 98 stars, based on 1 article reviews
digital camera olympus dp74 - by Bioz Stars, 2026-07
98/100 stars
  Buy from Supplier

90
Soft Imaging System GmbH cellsens software
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Cellsens Software, supplied by Soft Imaging System 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/product/olympus+cellsens+program/pm37371094-79-10-12?v=Soft+Imaging+System+GmbH
Average 90 stars, based on 1 article reviews
cellsens software - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

99
Olympus cellsens dimension 1 7 imaging software
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Cellsens Dimension 1 7 Imaging Software, supplied by Olympus, 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/product/olympus+cellsens+program/pm32002604-108-24-31?v=Olympus
Average 99 stars, based on 1 article reviews
cellsens dimension 1 7 imaging software - by Bioz Stars, 2026-07
99/100 stars
  Buy from Supplier

86
Olympus cellsens standard microscope imaging software
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Cellsens Standard Microscope Imaging Software, supplied by Olympus, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olympus+cellsens+program/pmc12691532-73-20-16?v=Olympus
Average 86 stars, based on 1 article reviews
cellsens standard microscope imaging software - by Bioz Stars, 2026-07
86/100 stars
  Buy from Supplier

86
Olympus cellsens fv software
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Cellsens Fv Software, supplied by Olympus, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/olympus+cellsens+program/pmc12743476-81-11-14?v=Olympus
Average 86 stars, based on 1 article reviews
cellsens fv software - by Bioz Stars, 2026-07
86/100 stars
  Buy from Supplier

96
Olympus cellsens entry software
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Cellsens Entry Software, supplied by Olympus, 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/product/olympus+cellsens+program/10__1021_slash_acsabm__0c01333-109-25-30?v=Olympus
Average 96 stars, based on 1 article reviews
cellsens entry software - by Bioz Stars, 2026-07
96/100 stars
  Buy from Supplier

90
GraphPad Software Inc graphpad prism 9.0
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Graphpad Prism 9.0, 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/product/olympus+cellsens+program/pm36685041-247-1-3?v=GraphPad+Software+Inc
Average 90 stars, based on 1 article reviews
graphpad prism 9.0 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
Hamamatsu hamamatsu orca-flash4.0
a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an <t>LV200</t> luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.
Hamamatsu Orca Flash4.0, 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
https://www.bioz.com/product/olympus+cellsens+program/pmc11371643-118-4-8?v=Hamamatsu
Average 90 stars, based on 1 article reviews
hamamatsu orca-flash4.0 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an LV200 luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: Periodic formation of epithelial somites from human pluripotent stem cells

doi: 10.1038/s41467-022-29967-1

Figure Lengend Snippet: a, b Time-lapse images of the HES7 promoter-luciferase reporter activity in a representative somitoid. The starting point on day 4 was defined as time 0. See also Supplementary Movie . Scale bars: 500 µm. Images were taken by an LV200 luminescent microscope. b Enlarged images of several time points are also shown. Arrows indicate the somite boundaries. BF: Bright field. c Kymograph of the HES7 reporter activity measured along the posterior-anterior axis (the white arrow) of the same sample shown in a , b . d Detrended intensity (top) and the oscillation phase (bottom) of the HES7 reporter activity in the same sample shown in a , b . Blue and orange lines indicate the signals measured in the posterior and anterior regions of somitoids, respectively, marked in c . The gaps in the graph correspond to short halts of imaging to adjust the sample position. N = 14 samples showed similar oscillatory patterns. e Relationship between HES7 oscillations and segmentation timings. Detrended HES7 reporter activity of the entire image of the same sample shown in a and b. Arrows indicate the timings of somite formation, and the colors correspond to the arrows in b . f Periods calculated from the HES7 oscillations and somite formation. Mean ± SEM. Each point in the graph indicates an average period of several oscillation peaks or somite formation timings in one sample from day 5 to day 6. N = 14 (HES7 oscillation) and 17 (Somite formation). 5 independent experiments. P -value is from two-sided student’s t-test. Source data are provided as a Source Data file.

Article Snippet: Live-luminescence imaging was performed with an LV200 luminescent microscope (Olympus, cellSens Dimension software) using a 10x objective lens (UPLXAPO10X).

Techniques: Luciferase, Activity Assay, Microscopy, Imaging