frap data analyses Search Results


95
GE Healthcare fraction collector
Fraction Collector, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Carl Zeiss zen software blue edition
Zen Software Blue Edition, 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
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Average 90 stars, based on 1 article reviews
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GraphPad Software Inc frap recovery data analysis
Frap Recovery Data Analysis, supplied by GraphPad 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
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Average 90 stars, based on 1 article reviews
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Carl Zeiss frap module
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Frap Module, supplied by Carl Zeiss, 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/frap module/product/Carl Zeiss
Average 94 stars, based on 1 article reviews
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90
MetaMorph Inc image-analysis software metamorph discovery-1
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Image Analysis Software Metamorph Discovery 1, 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
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Average 90 stars, based on 1 article reviews
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94
Revvity frap data harmony 3 5 1
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Frap Data Harmony 3 5 1, supplied by Revvity, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
frap data harmony 3 5 1 - by Bioz Stars, 2026-06
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90
GraphPad Software Inc prism software v5.01
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Prism Software V5.01, supplied by GraphPad 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/result/prism software v5.01/product/GraphPad Software Inc
Average 90 stars, based on 1 article reviews
prism software v5.01 - by Bioz Stars, 2026-06
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90
Carl Zeiss frap plugin
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Frap Plugin, 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/result/frap plugin/product/Carl Zeiss
Average 90 stars, based on 1 article reviews
frap plugin - by Bioz Stars, 2026-06
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90
Carl Zeiss lsm 510 nlo system
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Lsm 510 Nlo 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
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90
Metrohm AG frequency response analysis (fra) method metrohm autolab
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Frequency Response Analysis (Fra) Method Metrohm Autolab, supplied by Metrohm AG, 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/frequency response analysis (fra) method metrohm autolab/product/Metrohm AG
Average 90 stars, based on 1 article reviews
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90
Chemie GmbH eco chemie frequency response analyzer (fra) 4.9 software
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Eco Chemie Frequency Response Analyzer (Fra) 4.9 Software, supplied by Chemie 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/result/eco chemie frequency response analyzer (fra) 4.9 software/product/Chemie GmbH
Average 90 stars, based on 1 article reviews
eco chemie frequency response analyzer (fra) 4.9 software - by Bioz Stars, 2026-06
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99
Nikon frap data analysis
a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching <t>(FRAP)</t> of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS <t>X</t> <t>software.</t> Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.
Frap Data Analysis, 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/frap data analysis/product/Nikon
Average 99 stars, based on 1 article reviews
frap data analysis - by Bioz Stars, 2026-06
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Image Search Results


a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching (FRAP) of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS X software. Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.

Journal: Nature Communications

Article Title: Wiskott-Aldrich syndrome protein forms nuclear condensates and regulates alternative splicing

doi: 10.1038/s41467-022-31220-8

Figure Lengend Snippet: a Top: schematic diagram of Cry2-based optogenetic constructs of WASP and its N-terminal (NT) and C-terminal (CT) IDRs (created with BioRender.com). The NT and CT locations are shown on the top of PONDR IDR prediction diagram. Bottom: time-lapse confocal images of HEK293 cells expressing photo-activated optogenetic constructs of WASP, NT, or CT following photoactivation. Scale bar = 2 µm. The experiment was repeated at least three times independently. b Confocal imaging of fusion of optoWASP optogenetic droplets after blue light activation. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. c Confocal images showing fluorescence recovery after photobleaching (FRAP) of optoWASP droplets. Time-lapse images of the region framed in the box are shown below. Scale bar = 2 µm. The experiment was repeated at least three times independently. d Representative single-plane confocal images and colocalization analysis of optoWASP droplets (N-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson correlation coefficient of colocalization (Pearson’s r ) was calculated using the Leica LAS X software. Analyzed image n = 17, data are shown as mean ± SD. e Representative single-plane confocal images and colocalization analysis of optoWASP droplets (C-terminal WASP) with endogenous SRSF2 and nascent RNA. Insets show the framed region in the images. Scale bar = 2 µm. The Pearson’s r was calculated using the Leica LAS X software. Analyzed image n = 15, data are shown as mean ± SD.

Article Snippet: After image acquisition, the data were analyzed using FRAP module installed in ZEISS software.

Techniques: Construct, Expressing, Imaging, Activation Assay, Fluorescence, Software