h gfp emsc Search Results


resource source identifier rabbit anti-gfp emsco/fisher a11122  (Developmental Studies Hybridoma Bank)
99
Developmental Studies Hybridoma Bank resource source identifier rabbit anti-gfp emsco/fisher a11122
Resource Source Identifier Rabbit Anti Gfp Emsco/Fisher A11122, supplied by Developmental Studies Hybridoma Bank, 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/resource source identifier rabbit anti-gfp emsco/fisher a11122/product/Developmental Studies Hybridoma Bank
Average 99 stars, based on 1 article reviews
resource source identifier rabbit anti-gfp emsco/fisher a11122 - by Bioz Stars, 2026-04
99/100 stars
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h gfp emsc  (TargetMol)
92
TargetMol h gfp emsc
H Gfp Emsc, supplied by TargetMol, 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/result/h gfp emsc/product/TargetMol
Average 92 stars, based on 1 article reviews
h gfp emsc - by Bioz Stars, 2026-04
92/100 stars
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gfp cortactin immunoprecipitation  (Proteintech)
93
Proteintech gfp cortactin immunoprecipitation
Gfp Cortactin Immunoprecipitation, supplied by Proteintech, 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/result/gfp cortactin immunoprecipitation/product/Proteintech
Average 93 stars, based on 1 article reviews
gfp cortactin immunoprecipitation - by Bioz Stars, 2026-04
93/100 stars
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gfp pbf  (OriGene)
90
OriGene gfp pbf
<t>PBF</t> and CTTN colocalize at the leading edge in actively migrating cells. A, Representative confocal images showing endogenous CTTN (green), exogenous PBF (red) and colocalization (yellow) in SW1736 and MDA-MB-231 cells. Framed areas in merge images are magnified in right panels and Pearson's colocalization coefficients indicated. Magnification, 100×. Scale bars, 20 μM. B, Representative image of live cell migration assay in TPC-1 cells transfected with either <t>GFP-tagged</t> PBF or GFP-VO and tracked over 16.5 h. Photomicrographs show the tracks of individual cells over time. Boxed areas are magnified (right panels). C, Representation of individual tracks within one movie illustrate the further distances traveled by PBF-transfected cells. D, Quantification of mean cell migration rate (μm/h) of TPC-1 cells (n = 79 VO vs n = 63 PBF cells). E, Representative confocal images showing endogenous CTTN (green), exogenous PBF (red) and colocalization (yellow) in MDA-MB-231 cells. Scratch wound migration assays were halted at 4 h. White arrows indicate direction of cell movement. Magnified image from framed area in merge shown in lower right panel and Pearson's colocalization coefficients indicated. F, PLA assays in TPC-1 and MDA-MB-231 cells halted during scratch wound assays showing specific binding between CTTN and PBF (red dots), predominately at the leading edge of migrating cells. Arrows indicate direction of wound healing. White indicates DAPI nuclear stain. Magnification, 63×. Scale bars, 10 μM.
Gfp Pbf, supplied by OriGene, 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/gfp pbf/product/OriGene
Average 90 stars, based on 1 article reviews
gfp pbf - by Bioz Stars, 2026-04
90/100 stars
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Image Search Results


PBF and CTTN colocalize at the leading edge in actively migrating cells. A, Representative confocal images showing endogenous CTTN (green), exogenous PBF (red) and colocalization (yellow) in SW1736 and MDA-MB-231 cells. Framed areas in merge images are magnified in right panels and Pearson's colocalization coefficients indicated. Magnification, 100×. Scale bars, 20 μM. B, Representative image of live cell migration assay in TPC-1 cells transfected with either GFP-tagged PBF or GFP-VO and tracked over 16.5 h. Photomicrographs show the tracks of individual cells over time. Boxed areas are magnified (right panels). C, Representation of individual tracks within one movie illustrate the further distances traveled by PBF-transfected cells. D, Quantification of mean cell migration rate (μm/h) of TPC-1 cells (n = 79 VO vs n = 63 PBF cells). E, Representative confocal images showing endogenous CTTN (green), exogenous PBF (red) and colocalization (yellow) in MDA-MB-231 cells. Scratch wound migration assays were halted at 4 h. White arrows indicate direction of cell movement. Magnified image from framed area in merge shown in lower right panel and Pearson's colocalization coefficients indicated. F, PLA assays in TPC-1 and MDA-MB-231 cells halted during scratch wound assays showing specific binding between CTTN and PBF (red dots), predominately at the leading edge of migrating cells. Arrows indicate direction of wound healing. White indicates DAPI nuclear stain. Magnification, 63×. Scale bars, 10 μM.

Journal: The Journal of Clinical Endocrinology and Metabolism

Article Title: Pro-invasive Effect of Proto-oncogene PBF Is Modulated by an Interaction with Cortactin

doi: 10.1210/jc.2016-1932

Figure Lengend Snippet: PBF and CTTN colocalize at the leading edge in actively migrating cells. A, Representative confocal images showing endogenous CTTN (green), exogenous PBF (red) and colocalization (yellow) in SW1736 and MDA-MB-231 cells. Framed areas in merge images are magnified in right panels and Pearson's colocalization coefficients indicated. Magnification, 100×. Scale bars, 20 μM. B, Representative image of live cell migration assay in TPC-1 cells transfected with either GFP-tagged PBF or GFP-VO and tracked over 16.5 h. Photomicrographs show the tracks of individual cells over time. Boxed areas are magnified (right panels). C, Representation of individual tracks within one movie illustrate the further distances traveled by PBF-transfected cells. D, Quantification of mean cell migration rate (μm/h) of TPC-1 cells (n = 79 VO vs n = 63 PBF cells). E, Representative confocal images showing endogenous CTTN (green), exogenous PBF (red) and colocalization (yellow) in MDA-MB-231 cells. Scratch wound migration assays were halted at 4 h. White arrows indicate direction of cell movement. Magnified image from framed area in merge shown in lower right panel and Pearson's colocalization coefficients indicated. F, PLA assays in TPC-1 and MDA-MB-231 cells halted during scratch wound assays showing specific binding between CTTN and PBF (red dots), predominately at the leading edge of migrating cells. Arrows indicate direction of wound healing. White indicates DAPI nuclear stain. Magnification, 63×. Scale bars, 10 μM.

Article Snippet: Plasmids expressing human Myc-CTTN (No. RC223259) and GFP-PBF (No. RG202109) were purchased from Origene (Rockwell).

Techniques: Cell Migration Assay, Transfection, Migration, Binding Assay, Staining