n sim structured illumination super resolution microscope system Search Results


90
Carl Zeiss superresolution microscopy system for structured illumination elysra s1
Superresolution Microscopy System For Structured Illumination Elysra S1, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pm25688134-341-11-14?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
superresolution microscopy system for structured illumination elysra s1 - by Bioz Stars, 2026-07
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90
Carl Zeiss zeiss axioplan2 microscope
Zeiss Axioplan2 Microscope, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pmc07766928-225-10-12?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
zeiss axioplan2 microscope - by Bioz Stars, 2026-07
90/100 stars
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90
Carl Zeiss structured illumination microscope elyra s.1
Structured Illumination Microscope Elyra S.1, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pm30054480-377-6-11?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
structured illumination microscope elyra s.1 - by Bioz Stars, 2026-07
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90
Carl Zeiss elyra ps1 structured illumination microscope
Elyra Ps1 Structured Illumination Microscope, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pmc04081318-488-8-7?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
elyra ps1 structured illumination microscope - by Bioz Stars, 2026-07
90/100 stars
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90
Carl Zeiss elyra super-resolution microscopy system
Elyra Super Resolution Microscopy System, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pmc10698143-266-10-9?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
elyra super-resolution microscopy system - by Bioz Stars, 2026-07
90/100 stars
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90
Carl Zeiss plan-apochromat 63x/1.4 oil dic m27 objective
S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured <t>illumination</t> <t>microscopy.</t> a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .
Plan Apochromat 63x/1.4 Oil Dic M27 Objective, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pmc07427965-119-9-17?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
plan-apochromat 63x/1.4 oil dic m27 objective - by Bioz Stars, 2026-07
90/100 stars
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90
Carl Zeiss 710 laser scanning confocal and structured illumination microscope
S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured <t>illumination</t> <t>microscopy.</t> a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .
710 Laser Scanning Confocal And Structured Illumination Microscope, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pmc04201284-203-22-16?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
710 laser scanning confocal and structured illumination microscope - by Bioz Stars, 2026-07
90/100 stars
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90
Carl Zeiss sim-apotome axioimagerm2
S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured <t>illumination</t> <t>microscopy.</t> a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .
Sim Apotome Axioimagerm2, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pmc08894849-101-1-5?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
sim-apotome axioimagerm2 - by Bioz Stars, 2026-07
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90
Carl Zeiss structured illumination microscopy (sim
S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured <t>illumination</t> <t>microscopy.</t> a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .
Structured Illumination Microscopy (Sim, supplied by Carl Zeiss, 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/n+sim+structured+illumination+super+resolution+microscope+system/pmc05328288-42-15-25?v=Carl+Zeiss
Average 90 stars, based on 1 article reviews
structured illumination microscopy (sim - by Bioz Stars, 2026-07
90/100 stars
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99
Nikon illumination microscopy
S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured <t>illumination</t> <t>microscopy.</t> a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .
Illumination Microscopy, 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/product/n+sim+structured+illumination+super+resolution+microscope+system/pmc08561380-229-5-8?v=Nikon
Average 99 stars, based on 1 article reviews
illumination microscopy - by Bioz Stars, 2026-07
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93
Nikon illumination microscope
S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured <t>illumination</t> <t>microscopy.</t> a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .
Illumination 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/product/n+sim+structured+illumination+super+resolution+microscope+system/pm37459547-266-10-13?v=Nikon
Average 93 stars, based on 1 article reviews
illumination microscope - by Bioz Stars, 2026-07
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99
Nikon n sim microscope system
S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured <t>illumination</t> <t>microscopy.</t> a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .
N Sim Microscope System, 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/product/n+sim+structured+illumination+super+resolution+microscope+system/pmc08324808-489-6-9?v=Nikon
Average 99 stars, based on 1 article reviews
n sim microscope system - by Bioz Stars, 2026-07
99/100 stars
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Image Search Results


S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured illumination microscopy. a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .

Journal: Nature Communications

Article Title: Reassessment of the distinctive geometry of Staphylococcus aureus cell division

doi: 10.1038/s41467-020-17940-9

Figure Lengend Snippet: S. aureus strain COL cells were initially stained with cell wall dye WGA-488 (green) and membrane dye Nile Red (magenta). Excess of non-bound WGA-488 was removed by washing and Nile Red was added again before cells were placed on a medium-containing agarose pad and imaged every 20 min by structured illumination microscopy. a The border of the WGA-488-labelled region provides information on the orientation of the previous division plane (solid line), while the Nile Red-labelled septum indicates the orientation of the current division plane (dotted line). The angle (α) between the solid and dotted lines corresponds to the angle between the two consecutive planes of division. b Histogram of the angle α formed between two consecutive planes of division shows that these planes are orthogonal (with an average deviation from 90° of 6.7°, n = 183 cells examined over three biological replicates). Source data are provided as a Source data file. c First, second and third division planes are indicated by solid, dashed and dotted lines, respectively, showing that in the cell indicated by the arrow the third division plane is parallel, not perpendicular, to the first plane of division. Scale bars, 1 μm. A full field of view can be accessed in https://figshare.com/s/4808495d92a138aae36c .

Article Snippet: Time-lapse images were acquired every 20 min by structured illumination microscopy (SIM) in an Elyra PS.1 microscope (Zeiss) using a Plan-Apochromat 63x/1.4 oil DIC M27 objective.

Techniques: Staining, Membrane, Microscopy