ni e c2 microscope Search Results


confocal microscope  (Nikon)
90
Nikon confocal microscope
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/confocal microscope/product/Nikon
Average 90 stars, based on 1 article reviews
confocal microscope - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
nikon ni e c2 microscope  (Nikon)
99
Nikon nikon ni e c2 microscope
Nikon Ni E C2 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/nikon ni e c2 microscope/product/Nikon
Average 99 stars, based on 1 article reviews
nikon ni e c2 microscope - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier
nikon microscrope ni e c2  (Nikon)
99
Nikon nikon microscrope ni e c2
Nikon Microscrope Ni E C2, 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/nikon microscrope ni e c2/product/Nikon
Average 99 stars, based on 1 article reviews
nikon microscrope ni e c2 - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier
ni e c2 microscope  (Nikon)
99
Nikon ni e c2 microscope
Ni E C2 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/ni e c2 microscope/product/Nikon
Average 99 stars, based on 1 article reviews
ni e c2 microscope - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier
confocal laser scanning microscope nikon c2-nie  (Nikon)
90
Nikon confocal laser scanning microscope nikon c2-nie
Confocal Laser Scanning Microscope Nikon C2 Nie, 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 laser scanning microscope nikon c2-nie/product/Nikon
Average 90 stars, based on 1 article reviews
confocal laser scanning microscope nikon c2-nie - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
clsm nikon eclipse ni-e c2  (Nikon)
90
Nikon clsm nikon eclipse ni-e c2
Clsm Nikon Eclipse Ni E C2, 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/clsm nikon eclipse ni-e c2/product/Nikon
Average 90 stars, based on 1 article reviews
clsm nikon eclipse ni-e c2 - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
upright confocal microscope nikon instruments eclipse ni-e with a c2 confocal laser scanner  (Nikon)
90
Nikon upright confocal microscope nikon instruments eclipse ni-e with a c2 confocal laser scanner
Validation of cell–matrix interaction with different cell lines stably expressing OptoIntegrin. a HEK-293T, HeLa and MCF7 cells stably expressing OptoIntegrin or moxGFP-PIF S were seeded on PhyB 1–651 -coated glass slides and incubated under 660 nm or 740 nm light (I = 20 µmol m −2 s −1 ) for 5 h and subsequently imaged using a transmission light <t>microscope</t> (scale bar = 200 µm). b Live cell imaging of cell–matrix interaction under 660 nm light and then switch to 740 nm light after 35 min with binary images of cell shapes to illustrate the cells spreading. For this, HeLa cells stably expressing OptoIntegrin were seeded on OptoMatrix and subsequently imaged. Micrographs were taken at indicated time points (scale bar = 10 µm). c Spatial control of cell attachment with OptoIntegrin-expressing HEK-293T cells. OptoIntegrin-expressing cells were cultivated on OptoMatrix, locally illuminated with 660 nm or 740 nm for 3 min and then left in darkness for 4 h. Afterwards, cells were fixed and imaged (scale bar = 200 µm)
Upright Confocal Microscope Nikon Instruments Eclipse Ni E With A C2 Confocal Laser Scanner, 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/upright confocal microscope nikon instruments eclipse ni-e with a c2 confocal laser scanner/product/Nikon
Average 90 stars, based on 1 article reviews
upright confocal microscope nikon instruments eclipse ni-e with a c2 confocal laser scanner - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
fluoview fv1000 upright confocal microscope  (Evident Corporation)
90
Evident Corporation fluoview fv1000 upright confocal microscope
Validation of cell–matrix interaction with different cell lines stably expressing OptoIntegrin. a HEK-293T, HeLa and MCF7 cells stably expressing OptoIntegrin or moxGFP-PIF S were seeded on PhyB 1–651 -coated glass slides and incubated under 660 nm or 740 nm light (I = 20 µmol m −2 s −1 ) for 5 h and subsequently imaged using a transmission light <t>microscope</t> (scale bar = 200 µm). b Live cell imaging of cell–matrix interaction under 660 nm light and then switch to 740 nm light after 35 min with binary images of cell shapes to illustrate the cells spreading. For this, HeLa cells stably expressing OptoIntegrin were seeded on OptoMatrix and subsequently imaged. Micrographs were taken at indicated time points (scale bar = 10 µm). c Spatial control of cell attachment with OptoIntegrin-expressing HEK-293T cells. OptoIntegrin-expressing cells were cultivated on OptoMatrix, locally illuminated with 660 nm or 740 nm for 3 min and then left in darkness for 4 h. Afterwards, cells were fixed and imaged (scale bar = 200 µm)
Fluoview Fv1000 Upright Confocal 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
https://www.bioz.com/result/fluoview fv1000 upright confocal microscope/product/Evident Corporation
Average 90 stars, based on 1 article reviews
fluoview fv1000 upright confocal microscope - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
nie c2 upright confocal imaging system  (Nikon)
90
Nikon nie c2 upright confocal imaging system
Validation of cell–matrix interaction with different cell lines stably expressing OptoIntegrin. a HEK-293T, HeLa and MCF7 cells stably expressing OptoIntegrin or moxGFP-PIF S were seeded on PhyB 1–651 -coated glass slides and incubated under 660 nm or 740 nm light (I = 20 µmol m −2 s −1 ) for 5 h and subsequently imaged using a transmission light <t>microscope</t> (scale bar = 200 µm). b Live cell imaging of cell–matrix interaction under 660 nm light and then switch to 740 nm light after 35 min with binary images of cell shapes to illustrate the cells spreading. For this, HeLa cells stably expressing OptoIntegrin were seeded on OptoMatrix and subsequently imaged. Micrographs were taken at indicated time points (scale bar = 10 µm). c Spatial control of cell attachment with OptoIntegrin-expressing HEK-293T cells. OptoIntegrin-expressing cells were cultivated on OptoMatrix, locally illuminated with 660 nm or 740 nm for 3 min and then left in darkness for 4 h. Afterwards, cells were fixed and imaged (scale bar = 200 µm)
Nie C2 Upright Confocal Imaging 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
https://www.bioz.com/result/nie c2 upright confocal imaging system/product/Nikon
Average 90 stars, based on 1 article reviews
nie c2 upright confocal imaging system - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
confocal microscopy c2+ on a nikon eclipse ni-e, 60x 1.4na  (Nikon)
90
Nikon confocal microscopy c2+ on a nikon eclipse ni-e, 60x 1.4na
Validation of cell–matrix interaction with different cell lines stably expressing OptoIntegrin. a HEK-293T, HeLa and MCF7 cells stably expressing OptoIntegrin or moxGFP-PIF S were seeded on PhyB 1–651 -coated glass slides and incubated under 660 nm or 740 nm light (I = 20 µmol m −2 s −1 ) for 5 h and subsequently imaged using a transmission light <t>microscope</t> (scale bar = 200 µm). b Live cell imaging of cell–matrix interaction under 660 nm light and then switch to 740 nm light after 35 min with binary images of cell shapes to illustrate the cells spreading. For this, HeLa cells stably expressing OptoIntegrin were seeded on OptoMatrix and subsequently imaged. Micrographs were taken at indicated time points (scale bar = 10 µm). c Spatial control of cell attachment with OptoIntegrin-expressing HEK-293T cells. OptoIntegrin-expressing cells were cultivated on OptoMatrix, locally illuminated with 660 nm or 740 nm for 3 min and then left in darkness for 4 h. Afterwards, cells were fixed and imaged (scale bar = 200 µm)
Confocal Microscopy C2+ On A Nikon Eclipse Ni E, 60x 1.4na, 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 c2+ on a nikon eclipse ni-e, 60x 1.4na/product/Nikon
Average 90 stars, based on 1 article reviews
confocal microscopy c2+ on a nikon eclipse ni-e, 60x 1.4na - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
confocal fluorescence microscope c2/ni-e  (Nikon)
90
Nikon confocal fluorescence microscope c2/ni-e
Validation of cell–matrix interaction with different cell lines stably expressing OptoIntegrin. a HEK-293T, HeLa and MCF7 cells stably expressing OptoIntegrin or moxGFP-PIF S were seeded on PhyB 1–651 -coated glass slides and incubated under 660 nm or 740 nm light (I = 20 µmol m −2 s −1 ) for 5 h and subsequently imaged using a transmission light <t>microscope</t> (scale bar = 200 µm). b Live cell imaging of cell–matrix interaction under 660 nm light and then switch to 740 nm light after 35 min with binary images of cell shapes to illustrate the cells spreading. For this, HeLa cells stably expressing OptoIntegrin were seeded on OptoMatrix and subsequently imaged. Micrographs were taken at indicated time points (scale bar = 10 µm). c Spatial control of cell attachment with OptoIntegrin-expressing HEK-293T cells. OptoIntegrin-expressing cells were cultivated on OptoMatrix, locally illuminated with 660 nm or 740 nm for 3 min and then left in darkness for 4 h. Afterwards, cells were fixed and imaged (scale bar = 200 µm)
Confocal Fluorescence Microscope C2/Ni 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/confocal fluorescence microscope c2/ni-e/product/Nikon
Average 90 stars, based on 1 article reviews
confocal fluorescence microscope c2/ni-e - by Bioz Stars, 2026-05
90/100 stars
  Buy from Supplier
eclipse ni e c2 confocal microscope  (Nikon)
99
Nikon eclipse ni e c2 confocal microscope
Validation of cell–matrix interaction with different cell lines stably expressing OptoIntegrin. a HEK-293T, HeLa and MCF7 cells stably expressing OptoIntegrin or moxGFP-PIF S were seeded on PhyB 1–651 -coated glass slides and incubated under 660 nm or 740 nm light (I = 20 µmol m −2 s −1 ) for 5 h and subsequently imaged using a transmission light <t>microscope</t> (scale bar = 200 µm). b Live cell imaging of cell–matrix interaction under 660 nm light and then switch to 740 nm light after 35 min with binary images of cell shapes to illustrate the cells spreading. For this, HeLa cells stably expressing OptoIntegrin were seeded on OptoMatrix and subsequently imaged. Micrographs were taken at indicated time points (scale bar = 10 µm). c Spatial control of cell attachment with OptoIntegrin-expressing HEK-293T cells. OptoIntegrin-expressing cells were cultivated on OptoMatrix, locally illuminated with 660 nm or 740 nm for 3 min and then left in darkness for 4 h. Afterwards, cells were fixed and imaged (scale bar = 200 µm)
Eclipse Ni E C2 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/eclipse ni e c2 confocal microscope/product/Nikon
Average 99 stars, based on 1 article reviews
eclipse ni e c2 confocal microscope - by Bioz Stars, 2026-05
99/100 stars
  Buy from Supplier

Image Search Results


Validation of cell–matrix interaction with different cell lines stably expressing OptoIntegrin. a HEK-293T, HeLa and MCF7 cells stably expressing OptoIntegrin or moxGFP-PIF S were seeded on PhyB 1–651 -coated glass slides and incubated under 660 nm or 740 nm light (I = 20 µmol m −2 s −1 ) for 5 h and subsequently imaged using a transmission light microscope (scale bar = 200 µm). b Live cell imaging of cell–matrix interaction under 660 nm light and then switch to 740 nm light after 35 min with binary images of cell shapes to illustrate the cells spreading. For this, HeLa cells stably expressing OptoIntegrin were seeded on OptoMatrix and subsequently imaged. Micrographs were taken at indicated time points (scale bar = 10 µm). c Spatial control of cell attachment with OptoIntegrin-expressing HEK-293T cells. OptoIntegrin-expressing cells were cultivated on OptoMatrix, locally illuminated with 660 nm or 740 nm for 3 min and then left in darkness for 4 h. Afterwards, cells were fixed and imaged (scale bar = 200 µm)

Journal: Communications Biology

Article Title: Optogenetic control of integrin-matrix interaction

doi: 10.1038/s42003-018-0264-7

Figure Lengend Snippet: Validation of cell–matrix interaction with different cell lines stably expressing OptoIntegrin. a HEK-293T, HeLa and MCF7 cells stably expressing OptoIntegrin or moxGFP-PIF S were seeded on PhyB 1–651 -coated glass slides and incubated under 660 nm or 740 nm light (I = 20 µmol m −2 s −1 ) for 5 h and subsequently imaged using a transmission light microscope (scale bar = 200 µm). b Live cell imaging of cell–matrix interaction under 660 nm light and then switch to 740 nm light after 35 min with binary images of cell shapes to illustrate the cells spreading. For this, HeLa cells stably expressing OptoIntegrin were seeded on OptoMatrix and subsequently imaged. Micrographs were taken at indicated time points (scale bar = 10 µm). c Spatial control of cell attachment with OptoIntegrin-expressing HEK-293T cells. OptoIntegrin-expressing cells were cultivated on OptoMatrix, locally illuminated with 660 nm or 740 nm for 3 min and then left in darkness for 4 h. Afterwards, cells were fixed and imaged (scale bar = 200 µm)

Article Snippet: Finally, the stained coverslips were mounted on microscope slides with Mowiol 4-88 (Carl Roth, cat. no.: 0713), and confocal images were acquired on an upright confocal microscope (Nikon Instruments Eclipse Ni-E with a C2 confocal laser scanner, 100 × oil objective NA = 1.45 or 60× oil objective NA = 1.40).

Techniques: Biomarker Discovery, Stable Transfection, Expressing, Incubation, Transmission Assay, Light Microscopy, Live Cell Imaging, Control, Cell Attachment Assay