eclipse ti2 inverted compound microscope Search Results


csu w1 spinning disk confocal  (Yokogawa Electric)
99
Yokogawa Electric csu w1 spinning disk confocal
Csu W1 Spinning Disk Confocal, supplied by Yokogawa Electric, 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/csu w1 spinning disk confocal/product/Yokogawa Electric
Average 99 stars, based on 1 article reviews
csu w1 spinning disk confocal - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier
andor dragonfly spinning disk  (Oxford Instruments)
99
Oxford Instruments andor dragonfly spinning disk
Andor Dragonfly Spinning Disk, 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/result/andor dragonfly spinning disk/product/Oxford Instruments
Average 99 stars, based on 1 article reviews
andor dragonfly spinning disk - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier
inverted fluorescence microscope  (Nikon)
99
Nikon inverted fluorescence microscope
Inverted Fluorescence 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/inverted fluorescence microscope/product/Nikon
Average 99 stars, based on 1 article reviews
inverted fluorescence microscope - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier
ti2 eclipse inverted microscope  (Nikon)
99
Nikon ti2 eclipse inverted microscope
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
Ti2 Eclipse Inverted 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/ti2 eclipse inverted microscope/product/Nikon
Average 99 stars, based on 1 article reviews
ti2 eclipse inverted microscope - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier
ti2 e epifluorescence inverted microscope  (Nikon)
93
Nikon ti2 e epifluorescence inverted microscope
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
Ti2 E Epifluorescence Inverted Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/ti2 e epifluorescence inverted microscope/product/Nikon
Average 93 stars, based on 1 article reviews
ti2 e epifluorescence inverted microscope - by Bioz Stars, 2026-06
93/100 stars
  Buy from Supplier
inverted nikon ti 2 e inverted microscopes  (Nikon)
99
Nikon inverted nikon ti 2 e inverted microscopes
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
Inverted Nikon Ti 2 E Inverted Microscopes, 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/inverted nikon ti 2 e inverted microscopes/product/Nikon
Average 99 stars, based on 1 article reviews
inverted nikon ti 2 e inverted microscopes - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier
eclipse ti2 inverted confocal microscope  (Nikon)
99
Nikon eclipse ti2 inverted confocal microscope
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
Eclipse Ti2 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/eclipse ti2 inverted confocal microscope/product/Nikon
Average 99 stars, based on 1 article reviews
eclipse ti2 inverted confocal microscope - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier
ti2 e inverted microscope 1  (Nikon)
99
Nikon ti2 e inverted microscope 1
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
Ti2 E Inverted Microscope 1, 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/ti2 e inverted microscope 1/product/Nikon
Average 99 stars, based on 1 article reviews
ti2 e inverted microscope 1 - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier
nikon ti2 inverted microscope  (Nikon)
94
Nikon nikon ti2 inverted microscope
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
Nikon Ti2 Inverted Microscope, supplied by Nikon, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/nikon ti2 inverted microscope/product/Nikon
Average 94 stars, based on 1 article reviews
nikon ti2 inverted microscope - by Bioz Stars, 2026-06
94/100 stars
  Buy from Supplier
csu w1 sora confocal scanning  (Yokogawa Electric)
99
Yokogawa Electric csu w1 sora confocal scanning
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
Csu W1 Sora Confocal Scanning, supplied by Yokogawa Electric, 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/csu w1 sora confocal scanning/product/Yokogawa Electric
Average 99 stars, based on 1 article reviews
csu w1 sora confocal scanning - by Bioz Stars, 2026-06
99/100 stars
  Buy from Supplier
a1r confocal microscope  (Nikon)
96
Nikon a1r confocal microscope
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
A1r Confocal Microscope, supplied by Nikon, 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/result/a1r confocal microscope/product/Nikon
Average 96 stars, based on 1 article reviews
a1r confocal microscope - by Bioz Stars, 2026-06
96/100 stars
  Buy from Supplier
flash 4.0 lt camera  (Hamamatsu)
90
Hamamatsu flash 4.0 lt camera
Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon <t>Ti2</t> eclipse inverted <t>microscope</t> with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.
Flash 4.0 Lt 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
https://www.bioz.com/result/flash 4.0 lt camera/product/Hamamatsu
Average 90 stars, based on 1 article reviews
flash 4.0 lt camera - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier

Image Search Results


Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.

Journal: STAR Protocols

Article Title: Protocol for extracting live blastoderm cells from embryos of annual killifish

doi: 10.1016/j.xpro.2023.102344

Figure Lengend Snippet: Yield of A. nigripinnis blastoderm cells (deep embryonic and EVL cells) extracted at early post epiboly stages (A) Quantification of cell viability after extraction using the Neubauer chamber. Live cells appear green as they retain Calcein-AM fluorophore. Large cells are EVL cells and small are deep cells. (B) Exemplary images of a quadrant of the Neubauer chamber (left) and enlarged view (right) illustrate how to recognize EVL and deep cells and how to distinguish between live cells (those that retain Calcein-AM – green arrows) and dead cells (without fluorescence – red arrow). Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 10× air objective with 0.30 NA. Scale bar: 100 μm. (C) Comparison of cell size allows distinguishing EVL (diameter above 10 μm) from deep cells (about 5 μm in diameter). Live cells also typically display cellular activities such as presence of cellular extrusion. Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 40× air objective with 0.95 NA. Scale bar: 20 μm.

Article Snippet: Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 10× air objective with 0.30 NA.

Techniques: Extraction, Fluorescence, Inverted Microscopy, Comparison

Journal: STAR Protocols

Article Title: Protocol for extracting live blastoderm cells from embryos of annual killifish

doi: 10.1016/j.xpro.2023.102344

Figure Lengend Snippet:

Article Snippet: Images were acquired using a Nikon Ti2 eclipse inverted microscope with a 10× air objective with 0.30 NA.

Techniques: Recombinant, Inverted Microscopy, Clinical Proteomics, Cell Culture, Sterility, Transferring