draq5 in pbs Search Results


99
Thermo Fisher draq5 fluorescent probe solution
Draq5 Fluorescent Probe Solution, supplied by Thermo Fisher, 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/draq5+in+pbs/PBS/pmc07104363-194-15-19
Average 99 stars, based on 1 article reviews
draq5 fluorescent probe solution - by Bioz Stars, 2026-10
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97
Miltenyi Biotec pbs
Pbs, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/draq5+in+pbs/DRAQ5+Staining+Solution/bio_rxiv__64898__2026__02__16__706237-241-10-17
Average 97 stars, based on 1 article reviews
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90
Biostatus draq5
Draq5, supplied by Biostatus, 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/draq5+in+pbs/draq5/pmc03412895-251-4-8
Average 90 stars, based on 1 article reviews
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99
Thermo Fisher draq5
(A) Time series of images showing scratch wound invasion of pancreatic ductal cells through Matrigel. Wound confluence is the percentage of wound area covered by cells. Color legend: green is the wound area, blue shows wound confluence in the wound area, and grey represents the confluent cells outside of the wound area. Scale, 300 μm. (B) Schematic illustration showing the modified scratch wound assay. Cells are plated on a layer of thin Matrigel and invade into the thick 3D matrix of overlaid Matrigel that fills the scratch wound. The line plot shows quantification of wound confluence over time. The dotted line indicates the 72 h time point, which we use to compare wound confluence values for statistical significance. The bar plot represents wound confluence at the 72 h time point. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. (C) Schematic illustration showing the transwell migration assay. Cells migrate through the 8 μm pores of a polycarbonate membrane in response to a chemoattractant on the opposite side of the membrane. Images of transwell migration assays showing <t>DRAQ5-labeled</t> nuclei of cells that migrate through the 8 μm pores of a polycarbonate membrane after 12 hours. Scale, 50 μm. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. All error bars represent standard errors. The significance of pairwise comparisons between cell lines is shown in panels B and C by the initial(s) of the cell lines that are significantly different where H: HPDE, Hs: Hs766T, M: MIA PaCa-2, and P: PANC-1. For example, in panel B, HPDE is significantly different (*p < 0.05) from Hs766T (Hs) and PANC-1 (P).
Draq5, supplied by Thermo Fisher, 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/draq5+in+pbs/Triton+X-100/pmc05866717-592-8-17
Average 99 stars, based on 1 article reviews
draq5 - by Bioz Stars, 2026-10
99/100 stars
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96
Cell Signaling Technology Inc draq5 dye
(A) Time series of images showing scratch wound invasion of pancreatic ductal cells through Matrigel. Wound confluence is the percentage of wound area covered by cells. Color legend: green is the wound area, blue shows wound confluence in the wound area, and grey represents the confluent cells outside of the wound area. Scale, 300 μm. (B) Schematic illustration showing the modified scratch wound assay. Cells are plated on a layer of thin Matrigel and invade into the thick 3D matrix of overlaid Matrigel that fills the scratch wound. The line plot shows quantification of wound confluence over time. The dotted line indicates the 72 h time point, which we use to compare wound confluence values for statistical significance. The bar plot represents wound confluence at the 72 h time point. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. (C) Schematic illustration showing the transwell migration assay. Cells migrate through the 8 μm pores of a polycarbonate membrane in response to a chemoattractant on the opposite side of the membrane. Images of transwell migration assays showing <t>DRAQ5-labeled</t> nuclei of cells that migrate through the 8 μm pores of a polycarbonate membrane after 12 hours. Scale, 50 μm. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. All error bars represent standard errors. The significance of pairwise comparisons between cell lines is shown in panels B and C by the initial(s) of the cell lines that are significantly different where H: HPDE, Hs: Hs766T, M: MIA PaCa-2, and P: PANC-1. For example, in panel B, HPDE is significantly different (*p < 0.05) from Hs766T (Hs) and PANC-1 (P).
Draq5 Dye, supplied by Cell Signaling Technology 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/draq5+in+pbs/DRAQ5/pmc06082736-220-4-6
Average 96 stars, based on 1 article reviews
draq5 dye - by Bioz Stars, 2026-10
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97
Cell Signaling Technology Inc pbs
(A) Time series of images showing scratch wound invasion of pancreatic ductal cells through Matrigel. Wound confluence is the percentage of wound area covered by cells. Color legend: green is the wound area, blue shows wound confluence in the wound area, and grey represents the confluent cells outside of the wound area. Scale, 300 μm. (B) Schematic illustration showing the modified scratch wound assay. Cells are plated on a layer of thin Matrigel and invade into the thick 3D matrix of overlaid Matrigel that fills the scratch wound. The line plot shows quantification of wound confluence over time. The dotted line indicates the 72 h time point, which we use to compare wound confluence values for statistical significance. The bar plot represents wound confluence at the 72 h time point. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. (C) Schematic illustration showing the transwell migration assay. Cells migrate through the 8 μm pores of a polycarbonate membrane in response to a chemoattractant on the opposite side of the membrane. Images of transwell migration assays showing <t>DRAQ5-labeled</t> nuclei of cells that migrate through the 8 μm pores of a polycarbonate membrane after 12 hours. Scale, 50 μm. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. All error bars represent standard errors. The significance of pairwise comparisons between cell lines is shown in panels B and C by the initial(s) of the cell lines that are significantly different where H: HPDE, Hs: Hs766T, M: MIA PaCa-2, and P: PANC-1. For example, in panel B, HPDE is significantly different (*p < 0.05) from Hs766T (Hs) and PANC-1 (P).
Pbs, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/draq5+in+pbs/Phosphate+Buffered+Saline/ppr0808764-173-32-37
Average 97 stars, based on 1 article reviews
pbs - by Bioz Stars, 2026-10
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99
Thermo Fisher fmat assay buffer
(A) Time series of images showing scratch wound invasion of pancreatic ductal cells through Matrigel. Wound confluence is the percentage of wound area covered by cells. Color legend: green is the wound area, blue shows wound confluence in the wound area, and grey represents the confluent cells outside of the wound area. Scale, 300 μm. (B) Schematic illustration showing the modified scratch wound assay. Cells are plated on a layer of thin Matrigel and invade into the thick 3D matrix of overlaid Matrigel that fills the scratch wound. The line plot shows quantification of wound confluence over time. The dotted line indicates the 72 h time point, which we use to compare wound confluence values for statistical significance. The bar plot represents wound confluence at the 72 h time point. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. (C) Schematic illustration showing the transwell migration assay. Cells migrate through the 8 μm pores of a polycarbonate membrane in response to a chemoattractant on the opposite side of the membrane. Images of transwell migration assays showing <t>DRAQ5-labeled</t> nuclei of cells that migrate through the 8 μm pores of a polycarbonate membrane after 12 hours. Scale, 50 μm. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. All error bars represent standard errors. The significance of pairwise comparisons between cell lines is shown in panels B and C by the initial(s) of the cell lines that are significantly different where H: HPDE, Hs: Hs766T, M: MIA PaCa-2, and P: PANC-1. For example, in panel B, HPDE is significantly different (*p < 0.05) from Hs766T (Hs) and PANC-1 (P).
Fmat Assay Buffer, supplied by Thermo Fisher, 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/draq5+in+pbs/Bovine+Serum+Albumin/us11746158-1151-7-25
Average 99 stars, based on 1 article reviews
fmat assay buffer - by Bioz Stars, 2026-10
99/100 stars
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90
Enzo Biochem draq5 dna stain
(A) Time series of images showing scratch wound invasion of pancreatic ductal cells through Matrigel. Wound confluence is the percentage of wound area covered by cells. Color legend: green is the wound area, blue shows wound confluence in the wound area, and grey represents the confluent cells outside of the wound area. Scale, 300 μm. (B) Schematic illustration showing the modified scratch wound assay. Cells are plated on a layer of thin Matrigel and invade into the thick 3D matrix of overlaid Matrigel that fills the scratch wound. The line plot shows quantification of wound confluence over time. The dotted line indicates the 72 h time point, which we use to compare wound confluence values for statistical significance. The bar plot represents wound confluence at the 72 h time point. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. (C) Schematic illustration showing the transwell migration assay. Cells migrate through the 8 μm pores of a polycarbonate membrane in response to a chemoattractant on the opposite side of the membrane. Images of transwell migration assays showing <t>DRAQ5-labeled</t> nuclei of cells that migrate through the 8 μm pores of a polycarbonate membrane after 12 hours. Scale, 50 μm. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. All error bars represent standard errors. The significance of pairwise comparisons between cell lines is shown in panels B and C by the initial(s) of the cell lines that are significantly different where H: HPDE, Hs: Hs766T, M: MIA PaCa-2, and P: PANC-1. For example, in panel B, HPDE is significantly different (*p < 0.05) from Hs766T (Hs) and PANC-1 (P).
Draq5 Dna Stain, supplied by Enzo Biochem, 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/draq5+in+pbs/draq5/pmc01594869-263-29-34
Average 90 stars, based on 1 article reviews
draq5 dna stain - by Bioz Stars, 2026-10
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99
Thermo Fisher draq5 dna staining solution
(A) Time series of images showing scratch wound invasion of pancreatic ductal cells through Matrigel. Wound confluence is the percentage of wound area covered by cells. Color legend: green is the wound area, blue shows wound confluence in the wound area, and grey represents the confluent cells outside of the wound area. Scale, 300 μm. (B) Schematic illustration showing the modified scratch wound assay. Cells are plated on a layer of thin Matrigel and invade into the thick 3D matrix of overlaid Matrigel that fills the scratch wound. The line plot shows quantification of wound confluence over time. The dotted line indicates the 72 h time point, which we use to compare wound confluence values for statistical significance. The bar plot represents wound confluence at the 72 h time point. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. (C) Schematic illustration showing the transwell migration assay. Cells migrate through the 8 μm pores of a polycarbonate membrane in response to a chemoattractant on the opposite side of the membrane. Images of transwell migration assays showing <t>DRAQ5-labeled</t> nuclei of cells that migrate through the 8 μm pores of a polycarbonate membrane after 12 hours. Scale, 50 μm. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. All error bars represent standard errors. The significance of pairwise comparisons between cell lines is shown in panels B and C by the initial(s) of the cell lines that are significantly different where H: HPDE, Hs: Hs766T, M: MIA PaCa-2, and P: PANC-1. For example, in panel B, HPDE is significantly different (*p < 0.05) from Hs766T (Hs) and PANC-1 (P).
Draq5 Dna Staining Solution, supplied by Thermo Fisher, 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/draq5+in+pbs/DNA/pm36316447-94-17-26
Average 99 stars, based on 1 article reviews
draq5 dna staining solution - by Bioz Stars, 2026-10
99/100 stars
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Image Search Results


(A) Time series of images showing scratch wound invasion of pancreatic ductal cells through Matrigel. Wound confluence is the percentage of wound area covered by cells. Color legend: green is the wound area, blue shows wound confluence in the wound area, and grey represents the confluent cells outside of the wound area. Scale, 300 μm. (B) Schematic illustration showing the modified scratch wound assay. Cells are plated on a layer of thin Matrigel and invade into the thick 3D matrix of overlaid Matrigel that fills the scratch wound. The line plot shows quantification of wound confluence over time. The dotted line indicates the 72 h time point, which we use to compare wound confluence values for statistical significance. The bar plot represents wound confluence at the 72 h time point. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. (C) Schematic illustration showing the transwell migration assay. Cells migrate through the 8 μm pores of a polycarbonate membrane in response to a chemoattractant on the opposite side of the membrane. Images of transwell migration assays showing DRAQ5-labeled nuclei of cells that migrate through the 8 μm pores of a polycarbonate membrane after 12 hours. Scale, 50 μm. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. All error bars represent standard errors. The significance of pairwise comparisons between cell lines is shown in panels B and C by the initial(s) of the cell lines that are significantly different where H: HPDE, Hs: Hs766T, M: MIA PaCa-2, and P: PANC-1. For example, in panel B, HPDE is significantly different (*p < 0.05) from Hs766T (Hs) and PANC-1 (P).

Journal: Integrative biology : quantitative biosciences from nano to macro

Article Title: Stiffness of pancreatic cancer cells is associated with increased invasive potential

doi: 10.1039/c6ib00135a

Figure Lengend Snippet: (A) Time series of images showing scratch wound invasion of pancreatic ductal cells through Matrigel. Wound confluence is the percentage of wound area covered by cells. Color legend: green is the wound area, blue shows wound confluence in the wound area, and grey represents the confluent cells outside of the wound area. Scale, 300 μm. (B) Schematic illustration showing the modified scratch wound assay. Cells are plated on a layer of thin Matrigel and invade into the thick 3D matrix of overlaid Matrigel that fills the scratch wound. The line plot shows quantification of wound confluence over time. The dotted line indicates the 72 h time point, which we use to compare wound confluence values for statistical significance. The bar plot represents wound confluence at the 72 h time point. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. (C) Schematic illustration showing the transwell migration assay. Cells migrate through the 8 μm pores of a polycarbonate membrane in response to a chemoattractant on the opposite side of the membrane. Images of transwell migration assays showing DRAQ5-labeled nuclei of cells that migrate through the 8 μm pores of a polycarbonate membrane after 12 hours. Scale, 50 μm. Pairwise p-values are determined by a Student’s t-test. *p < 0.05. All error bars represent standard errors. The significance of pairwise comparisons between cell lines is shown in panels B and C by the initial(s) of the cell lines that are significantly different where H: HPDE, Hs: Hs766T, M: MIA PaCa-2, and P: PANC-1. For example, in panel B, HPDE is significantly different (*p < 0.05) from Hs766T (Hs) and PANC-1 (P).

Article Snippet: To image the nucleus, cells are stained with DRAQ5 (1:250 in 0.3% Triton X-100 in 1x PBS; ThermoFisher) at room temperature for 20 minutes.

Techniques: Modification, Scratch Wound Assay Assay, Transwell Migration Assay, Migration, Labeling