volocity Search Results


volocity software  (Hamamatsu)
90
Hamamatsu volocity software
Volocity 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/volocity/volocity+software/pmc04214780-242-13-7
Average 90 stars, based on 1 article reviews
volocity software - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
volocity software  (Improvisions Inc)
90
Improvisions Inc volocity software
Volocity Software, supplied by Improvisions 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/volocity/volocity+software/pmc04326907-165-10-12
Average 90 stars, based on 1 article reviews
volocity software - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
improvision volocity software  (Hamamatsu)
90
Hamamatsu improvision volocity software
Improvision Volocity 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/volocity/improvision+volocity+software/pmc04397591-132-7-16
Average 90 stars, based on 1 article reviews
improvision volocity software - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
volocity software  (InterFocus GmbH)
90
InterFocus GmbH volocity software
Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “<half” class comprises nuclei that lack a SYP-1 aggregate but have SYP-1 associated with less than half of the total length of the autosomal axes (marked by HTP-3 immunostaining). Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Sample images from the analysis quantified in (A); images are maximum intensity projections generated in <t>Volocity</t> from 3-D image stacks (top, partial projection; bottom, full projection). Schematics in bottom left corner of DAPI panels indicate the portion of the nucleus included in the projection. Top, nucleus from the short-stretch category, showing two SYP-1 stretches that are clearly shorter than the length of a chromosome (↓), plus a large SYP-1 aggregate (*) that also contains (nonaxis-associated) HTP-3 protein. Bottom, characteristic image from the <half class. (C) Cumulative distribution event curves for autosomal synapsis, indicating that it takes ∼3–3.5 hr from the onset of autosomal synapsis until synapsis is complete (see text). Also plotted is the actual frequency (not cumulative distribution) of SYP-1 aggregates present at the indicated time points, which indicates that SYP-1 aggregates are present in essentially all leptotene nuclei, but disappear at or soon after the onset of synapsis. All error bars indicate 95% C.I. h, hours
Volocity Software, supplied by InterFocus 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/volocity/volocity+software/pmc05586365-75-7-0
Average 90 stars, based on 1 article reviews
volocity software - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
volocity 3-d image analysis software  (SciCrunch Inc)
90
SciCrunch Inc volocity 3-d image analysis software
Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “<half” class comprises nuclei that lack a SYP-1 aggregate but have SYP-1 associated with less than half of the total length of the autosomal axes (marked by HTP-3 immunostaining). Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Sample images from the analysis quantified in (A); images are maximum intensity projections generated in <t>Volocity</t> from 3-D image stacks (top, partial projection; bottom, full projection). Schematics in bottom left corner of DAPI panels indicate the portion of the nucleus included in the projection. Top, nucleus from the short-stretch category, showing two SYP-1 stretches that are clearly shorter than the length of a chromosome (↓), plus a large SYP-1 aggregate (*) that also contains (nonaxis-associated) HTP-3 protein. Bottom, characteristic image from the <half class. (C) Cumulative distribution event curves for autosomal synapsis, indicating that it takes ∼3–3.5 hr from the onset of autosomal synapsis until synapsis is complete (see text). Also plotted is the actual frequency (not cumulative distribution) of SYP-1 aggregates present at the indicated time points, which indicates that SYP-1 aggregates are present in essentially all leptotene nuclei, but disappear at or soon after the onset of synapsis. All error bars indicate 95% C.I. h, hours
Volocity 3 D Image Analysis Software, supplied by SciCrunch 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/volocity/volocity+3+d+image+analysis+software/pm38150545-80-9-16
Average 90 stars, based on 1 article reviews
volocity 3-d image analysis software - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
volocity acquisition software  (Hamamatsu)
90
Hamamatsu volocity acquisition software
Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “<half” class comprises nuclei that lack a SYP-1 aggregate but have SYP-1 associated with less than half of the total length of the autosomal axes (marked by HTP-3 immunostaining). Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Sample images from the analysis quantified in (A); images are maximum intensity projections generated in <t>Volocity</t> from 3-D image stacks (top, partial projection; bottom, full projection). Schematics in bottom left corner of DAPI panels indicate the portion of the nucleus included in the projection. Top, nucleus from the short-stretch category, showing two SYP-1 stretches that are clearly shorter than the length of a chromosome (↓), plus a large SYP-1 aggregate (*) that also contains (nonaxis-associated) HTP-3 protein. Bottom, characteristic image from the <half class. (C) Cumulative distribution event curves for autosomal synapsis, indicating that it takes ∼3–3.5 hr from the onset of autosomal synapsis until synapsis is complete (see text). Also plotted is the actual frequency (not cumulative distribution) of SYP-1 aggregates present at the indicated time points, which indicates that SYP-1 aggregates are present in essentially all leptotene nuclei, but disappear at or soon after the onset of synapsis. All error bars indicate 95% C.I. h, hours
Volocity Acquisition 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/volocity/volocity+acquisition+software/pm25666808-367-11-8
Average 90 stars, based on 1 article reviews
volocity acquisition software - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
volocity  (MetaMorph Inc)
90
MetaMorph Inc volocity
Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “<half” class comprises nuclei that lack a SYP-1 aggregate but have SYP-1 associated with less than half of the total length of the autosomal axes (marked by HTP-3 immunostaining). Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Sample images from the analysis quantified in (A); images are maximum intensity projections generated in <t>Volocity</t> from 3-D image stacks (top, partial projection; bottom, full projection). Schematics in bottom left corner of DAPI panels indicate the portion of the nucleus included in the projection. Top, nucleus from the short-stretch category, showing two SYP-1 stretches that are clearly shorter than the length of a chromosome (↓), plus a large SYP-1 aggregate (*) that also contains (nonaxis-associated) HTP-3 protein. Bottom, characteristic image from the <half class. (C) Cumulative distribution event curves for autosomal synapsis, indicating that it takes ∼3–3.5 hr from the onset of autosomal synapsis until synapsis is complete (see text). Also plotted is the actual frequency (not cumulative distribution) of SYP-1 aggregates present at the indicated time points, which indicates that SYP-1 aggregates are present in essentially all leptotene nuclei, but disappear at or soon after the onset of synapsis. All error bars indicate 95% C.I. h, hours
Volocity, supplied by MetaMorph 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/volocity/volocity/pm14623446-270-3-0
Average 90 stars, based on 1 article reviews
volocity - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
camera's volocity  (QED Imaging Inc)
90
QED Imaging Inc camera's volocity
Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “<half” class comprises nuclei that lack a SYP-1 aggregate but have SYP-1 associated with less than half of the total length of the autosomal axes (marked by HTP-3 immunostaining). Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Sample images from the analysis quantified in (A); images are maximum intensity projections generated in <t>Volocity</t> from 3-D image stacks (top, partial projection; bottom, full projection). Schematics in bottom left corner of DAPI panels indicate the portion of the nucleus included in the projection. Top, nucleus from the short-stretch category, showing two SYP-1 stretches that are clearly shorter than the length of a chromosome (↓), plus a large SYP-1 aggregate (*) that also contains (nonaxis-associated) HTP-3 protein. Bottom, characteristic image from the <half class. (C) Cumulative distribution event curves for autosomal synapsis, indicating that it takes ∼3–3.5 hr from the onset of autosomal synapsis until synapsis is complete (see text). Also plotted is the actual frequency (not cumulative distribution) of SYP-1 aggregates present at the indicated time points, which indicates that SYP-1 aggregates are present in essentially all leptotene nuclei, but disappear at or soon after the onset of synapsis. All error bars indicate 95% C.I. h, hours
Camera's Volocity, supplied by QED Imaging 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/volocity/camera+s+volocity/pmc03339966-102-6-14
Average 90 stars, based on 1 article reviews
camera's volocity - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
volocity software  (Velocity Software Inc)
90
Velocity Software Inc volocity software
Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “<half” class comprises nuclei that lack a SYP-1 aggregate but have SYP-1 associated with less than half of the total length of the autosomal axes (marked by HTP-3 immunostaining). Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Sample images from the analysis quantified in (A); images are maximum intensity projections generated in <t>Volocity</t> from 3-D image stacks (top, partial projection; bottom, full projection). Schematics in bottom left corner of DAPI panels indicate the portion of the nucleus included in the projection. Top, nucleus from the short-stretch category, showing two SYP-1 stretches that are clearly shorter than the length of a chromosome (↓), plus a large SYP-1 aggregate (*) that also contains (nonaxis-associated) HTP-3 protein. Bottom, characteristic image from the <half class. (C) Cumulative distribution event curves for autosomal synapsis, indicating that it takes ∼3–3.5 hr from the onset of autosomal synapsis until synapsis is complete (see text). Also plotted is the actual frequency (not cumulative distribution) of SYP-1 aggregates present at the indicated time points, which indicates that SYP-1 aggregates are present in essentially all leptotene nuclei, but disappear at or soon after the onset of synapsis. All error bars indicate 95% C.I. h, hours
Volocity Software, supplied by Velocity 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/volocity/volocity+software/pmc03256732-51-12-14
Average 90 stars, based on 1 article reviews
volocity software - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
volocity softwaretm  (Improvisions Inc)
90
Improvisions Inc volocity softwaretm
Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “<half” class comprises nuclei that lack a SYP-1 aggregate but have SYP-1 associated with less than half of the total length of the autosomal axes (marked by HTP-3 immunostaining). Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Sample images from the analysis quantified in (A); images are maximum intensity projections generated in <t>Volocity</t> from 3-D image stacks (top, partial projection; bottom, full projection). Schematics in bottom left corner of DAPI panels indicate the portion of the nucleus included in the projection. Top, nucleus from the short-stretch category, showing two SYP-1 stretches that are clearly shorter than the length of a chromosome (↓), plus a large SYP-1 aggregate (*) that also contains (nonaxis-associated) HTP-3 protein. Bottom, characteristic image from the <half class. (C) Cumulative distribution event curves for autosomal synapsis, indicating that it takes ∼3–3.5 hr from the onset of autosomal synapsis until synapsis is complete (see text). Also plotted is the actual frequency (not cumulative distribution) of SYP-1 aggregates present at the indicated time points, which indicates that SYP-1 aggregates are present in essentially all leptotene nuclei, but disappear at or soon after the onset of synapsis. All error bars indicate 95% C.I. h, hours
Volocity Softwaretm, supplied by Improvisions 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/volocity/volocity+softwaretm/pmc04064320-91-14-16
Average 90 stars, based on 1 article reviews
volocity softwaretm - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier

Image Search Results


Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “<half” class comprises nuclei that lack a SYP-1 aggregate but have SYP-1 associated with less than half of the total length of the autosomal axes (marked by HTP-3 immunostaining). Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Sample images from the analysis quantified in (A); images are maximum intensity projections generated in Volocity from 3-D image stacks (top, partial projection; bottom, full projection). Schematics in bottom left corner of DAPI panels indicate the portion of the nucleus included in the projection. Top, nucleus from the short-stretch category, showing two SYP-1 stretches that are clearly shorter than the length of a chromosome (↓), plus a large SYP-1 aggregate (*) that also contains (nonaxis-associated) HTP-3 protein. Bottom, characteristic image from the <half class. (C) Cumulative distribution event curves for autosomal synapsis, indicating that it takes ∼3–3.5 hr from the onset of autosomal synapsis until synapsis is complete (see text). Also plotted is the actual frequency (not cumulative distribution) of SYP-1 aggregates present at the indicated time points, which indicates that SYP-1 aggregates are present in essentially all leptotene nuclei, but disappear at or soon after the onset of synapsis. All error bars indicate 95% C.I. h, hours

Journal: Genetics

Article Title: Time-Course Analysis of Early Meiotic Prophase Events Informs Mechanisms of Homolog Pairing and Synapsis in Caenorhabditis elegans

doi: 10.1534/genetics.117.204172

Figure Lengend Snippet: Timing of synapsis for autosomes. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with autosomes at each time point (in nuclei with S-phase labeled X chromosomes). For nuclei in the “short stretch” class [example shown in (B)], one or a few short stretches of SYP-1 were observed, together with a large SYP-1 aggregate not associated with chromosome axes; it is unclear whether such short stretches represent bona fide synapsis intermediates. The “

Article Snippet: Interfocus distances reported in were measured using Volocity software. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window caption a7 Distinct organization of DAPI-stained chromatin during early meiotic prophase substages allows alignment of data from different experiments. (A–D) Left: immunofluorescence images of individual nuclei stained for DNA (DAPI); meiotic chromosome axis protein HTP-3; and SC central-region protein SYP-1, illustrating the DAPI organization features used to identify and define the indicated substages.

Techniques: Labeling, Immunostaining, Generated

Timing of X-chromosome synapsis. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with the X-chromosome pair at each time point. In the dot class, the only SYP-1 associated with the X chromosomes is a small dot that has clearly not been extended at all [example shown in (E)]; nuclei with any elongated SYP-1 stretch up to half the length of a chromosome pair comprise the “<half” class. Numbers of gonads/nuclei scored as reported in Figure 2 legend. (B) Cumulative distribution curves for X-chromosome synapsis (±95% C.I.). (C) Two-by-two contingency table depicting the incidence of fully synapsed autosomes relative to fully synapsed X chromosomes at the 5-hr postinjection time point, when essentially all of the nuclei were in the midzygotene stage. X chromosomes exhibiting complete synapsis were substantially underrepresented relative to autosomes (P < 0.0001, two-tailed Fisher exact test). (D) Image panel depicting a leptotene nucleus 4 hr postinjection with S-phase labeled X chromosomes, immunostained for axis protein HTP-3. Whereas HTP-3 is associated with all autosomes in this nucleus, HTP-3 is not yet detected on the X chromosomes, suggesting that axis assembly on the X chromosomes is delayed relative to autosomal axis assembly. (E) Image panel of a zygotene nucleus from a “shadow time point” 8.5 hr postinjection, in which S-phase label had been incorporated into all autosomes during early S phase but not into the HIM-8-marked X chromosomes (as label had been depleted prior to the start of X replication). Whereas there is extensive SYP-1 associated with the autosomes in this nucleus, only a tiny SYP-1 dot is detected on the X (arrow). This image panel illustrates that later timing of SC assembly on the X chromosomes (relative to the autosomes) is not an experimental artifact resulting from incorporation of labeled nucleotides into the DNA. Images in (D and E) are from Volocity volume renderings of 3-D data stacks encompassing whole nuclei. Blue outlines indicate the X chromosomes; dNTP* indicates labeled nucleotides. h, hours; org., organization.

Journal: Genetics

Article Title: Time-Course Analysis of Early Meiotic Prophase Events Informs Mechanisms of Homolog Pairing and Synapsis in Caenorhabditis elegans

doi: 10.1534/genetics.117.204172

Figure Lengend Snippet: Timing of X-chromosome synapsis. (A) Stacked bar graph indicating the percent of nuclei exhibiting the indicated patterns of SYP-1 localization associated with the X-chromosome pair at each time point. In the dot class, the only SYP-1 associated with the X chromosomes is a small dot that has clearly not been extended at all [example shown in (E)]; nuclei with any elongated SYP-1 stretch up to half the length of a chromosome pair comprise the “

Article Snippet: Interfocus distances reported in were measured using Volocity software. fig ft0 fig mode=article f1 fig/graphic|fig/alternatives/graphic mode="anchored" m1 Open in a separate window caption a7 Distinct organization of DAPI-stained chromatin during early meiotic prophase substages allows alignment of data from different experiments. (A–D) Left: immunofluorescence images of individual nuclei stained for DNA (DAPI); meiotic chromosome axis protein HTP-3; and SC central-region protein SYP-1, illustrating the DAPI organization features used to identify and define the indicated substages.

Techniques: Two Tailed Test, Labeling