deltavision Search Results


deltavision ultra high resolution microscope  (GE Healthcare)
91
GE Healthcare deltavision ultra high resolution microscope
Deltavision Ultra High Resolution Microscope, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/deltavision/DeltaVision+Ultra+with+benchtop+platform/ppr0352068-85-0-4
Average 91 stars, based on 1 article reviews
deltavision ultra high resolution microscope - by Bioz Stars, 2026-10
91/100 stars
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deltavision omx imaging system  (Danaher Inc)
96
Danaher Inc deltavision omx imaging system
Deltavision Omx Imaging System, supplied by Danaher Inc, 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/deltavision/DeltaVision+OMX+SR/pmc06761166-314-9-13
Average 96 stars, based on 1 article reviews
deltavision omx imaging system - by Bioz Stars, 2026-10
96/100 stars
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deltavision omx microscope  (Danaher Inc)
92
Danaher Inc deltavision omx microscope
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Deltavision Omx Microscope, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/deltavision/DeltaVision+OMX+Flex/pmc07108666-555-13-16
Average 92 stars, based on 1 article reviews
deltavision omx microscope - by Bioz Stars, 2026-10
92/100 stars
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fcs2 stage adapter  (Bioptechs inc)
93
Bioptechs inc fcs2 stage adapter
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Fcs2 Stage Adapter, supplied by Bioptechs inc, 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/deltavision/FCS2+Stage+Adapters+Nikon%2C+Olympus%2C+Deltavision+Adapter/pmc10316746__NIHMS1900743___supplement___Supp_Text-153-15-18
Average 93 stars, based on 1 article reviews
fcs2 stage adapter - by Bioz Stars, 2026-10
93/100 stars
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deltavision omx sr imaging system  (TOPTICA Photonics)
90
TOPTICA Photonics deltavision omx sr imaging system
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Deltavision Omx Sr Imaging System, supplied by TOPTICA Photonics, 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/deltavision/deltavision+omx+sr+imaging+system/pm38678366-327-6-36
Average 90 stars, based on 1 article reviews
deltavision omx sr imaging system - by Bioz Stars, 2026-10
90/100 stars
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deltavision softworks analysis software  (Softworks Group Inc)
90
Softworks Group Inc deltavision softworks analysis software
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Deltavision Softworks Analysis Software, supplied by Softworks Group 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/deltavision/deltavision+softworks+analysis+software/pmc04761827-107-18-19
Average 90 stars, based on 1 article reviews
deltavision softworks analysis software - by Bioz Stars, 2026-10
90/100 stars
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deltavision aquacosmos software  (Hamamatsu)
90
Hamamatsu deltavision aquacosmos software
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Deltavision Aquacosmos Software, 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/deltavision/deltavision+aquacosmos+software/pm17295841-196-17-20
Average 90 stars, based on 1 article reviews
deltavision aquacosmos software - by Bioz Stars, 2026-10
90/100 stars
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deltavision core-sp microscope  (Berthold Australia Pty)
90
Berthold Australia Pty deltavision core-sp microscope
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Deltavision Core Sp Microscope, supplied by Berthold Australia Pty, 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/deltavision/deltavision+core+sp+microscope/pmc04773363-21-29-23
Average 90 stars, based on 1 article reviews
deltavision core-sp microscope - by Bioz Stars, 2026-10
90/100 stars
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deltavision elite with truelight deconvolution microscope  (Truelight Corporation)
90
Truelight Corporation deltavision elite with truelight deconvolution microscope
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Deltavision Elite With Truelight Deconvolution Microscope, supplied by Truelight 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/product/deltavision/deltavision+elite+with+truelight+deconvolution+microscope/pmc05909929-250-26-25
Average 90 stars, based on 1 article reviews
deltavision elite with truelight deconvolution microscope - by Bioz Stars, 2026-10
90/100 stars
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deltavision  (Seki Technotron Corp)
90
Seki Technotron Corp deltavision
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Deltavision, supplied by Seki Technotron Corp, 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/deltavision/deltavision/pm20970334-133-27-30
Average 90 stars, based on 1 article reviews
deltavision - by Bioz Stars, 2026-10
90/100 stars
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inverted deltavision microscope  (MatTek)
90
MatTek inverted deltavision microscope
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
Inverted Deltavision Microscope, supplied by MatTek, 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/deltavision/inverted+deltavision+microscope/pmc02693489-162-12-22
Average 90 stars, based on 1 article reviews
inverted deltavision microscope - by Bioz Stars, 2026-10
90/100 stars
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the deltavision system  (Solent Scientific Ltd)
90
Solent Scientific Ltd the deltavision system
(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a <t>DeltaVision</t> <t>OMX</t> high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).
The Deltavision System, supplied by Solent Scientific Ltd, 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/deltavision/the+deltavision+system/pmc02277235-130-1-15
Average 90 stars, based on 1 article reviews
the deltavision system - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


(A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a DeltaVision OMX high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).

Journal: Developmental cell

Article Title: Mechanism of Long-Range Chromosome Motion Triggered by Gene Activation

doi: 10.1016/j.devcel.2019.12.007

Figure Lengend Snippet: (A) The position of INO1 in parental or cells deficient in an SWR-C ARP subunit (arp6Δ) or INO80-C ARP subunits (arp8Δ and ies6Δ as it results in loss of the Arp5-module) were monitored in the presence (+) and absence (−) of inositol (n = 3). (B) Parental yeast were treated with the carrier (DMSO) or Latrunculin-A (Lat-A) for 30 min then shifted to inositol free media. INO1 nuclear position was determined before (+) or after 30 min or 3 h of inositol starvation (−) (n = 3). (C) The INO1 GFP-marked yeast were transformed with an expression vector for an actin chromobody and examined using a DeltaVision OMX high-resolution microscope. The outer and nuclear membrane is visualized with ER05-mCherry and the bright green spot in the nucleus is the GFP-marked INO1 locus. (D) The nuclear actin signal was observed using an Airyscan confocal microscope. A still image captured from a high-speed Video (Video S7) is shown. (E) To assess the dynamic properties of the nuclear actin the images from 4 consecutive frames of an Airyscan video were averaged. A still image from Video S8 is shown. (F) The influence of expressing wild type actin fused to an NLS or the actin polymerization mutant R62D was checked in parental INO1-marked yeast in the presence (+) and absence (−) of inositol, as indicated (n = 3).

Article Snippet: Microscopy INO1 nuclear positioning was determined by analyzing z-stack images acquired with a DeltaVision OMX microscope (GE Life Science) with 100x/1.40 NA oil immersion objective (Olympus).

Techniques: Transformation Assay, Expressing, Plasmid Preparation, Microscopy, Mutagenesis