negative selection marker expressing tagbfp Search Results


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a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of <t>a</t> <t>TagBFP-NLS-expressing</t> HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).
Tagbfp, supplied by Twist Bioscience, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of <t>a</t> <t>TagBFP-NLS-expressing</t> HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).
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a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of <t>a</t> <t>TagBFP-NLS-expressing</t> HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).
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Sangon Biotech n × alfa p2a tagbfp fragment
a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of <t>a</t> <t>TagBFP-NLS-expressing</t> HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).
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Addgene inc plenticrispr tagbfp
a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of <t>a</t> <t>TagBFP-NLS-expressing</t> HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).
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a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of <t>a</t> <t>TagBFP-NLS-expressing</t> HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).
T2a.Tagbfp Plasmid Dna, supplied by Lonza, 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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VectorBuilder GmbH virus particles harboring the tagbfp-rxrα gene
a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of <t>a</t> <t>TagBFP-NLS-expressing</t> HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).
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VectorBuilder GmbH prp[exp]-cag > tagbfp

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Image Search Results


a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of a TagBFP-NLS-expressing HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).

Journal: Nature Photonics

Article Title: Multispectral live-cell imaging with uncompromised spatiotemporal resolution

doi: 10.1038/s41566-025-01745-7

Figure Lengend Snippet: a , Schematic depicting the use of fluorescently labelled, computationally designed receptor binders for imaging receptor trafficking. b , Single frame of the RLSU unmixed results (Supplementary Video ) of a TagBFP-NLS-expressing HeLa Kyoto cell loaded with four fluorescently labelled binders (TfRB, IGF2RB, BMPR2B and Iα5β1B) and one fluorescently labelled receptor ligand (EGF). Top–down and orthogonal-view maximum intensity projections are shown (cell boundaries in cyan). c , Colour merge of the channels in b . d , Individual channels and colour merge of the endosomes indicated by yellow, green, magenta and cyan boxes in c . e , Individual channels and colour merge of a single endosome during cargo sorting. Frames from Supplementary Video displaying fissioning of this compartment are shown. Magenta dashed circles indicate the parent endosome (labelled ‘1’). Cyan arrowheads indicate the elongation of an intermediate tubule. Red and cyan circles indicate the two daughter endosomes post-fissioning (labelled ‘2.a’ and ‘2.b’, respectively). f , Graph depicting the average proportion of total endosomes ( n = 1,872) containing each cargo across the first five frames of Supplementary Video . Error bars denote s.d. g , Individual channels and colour merge of a highly motile endosome at t = 0. h , Colour merge of the endosome in g undergoing directional transport. i , Kymographs of the highly motile endosome shown in g and h . j , Graph depicting the cargo proportion transferred from the the parent endosome (magenta dashed circle, endosome 1) to each daughter endosome post-fissioning (red and cyan dashed circles, endosomes 2.a and 2.b, respectively) in e . Scale bars, 5 μm ( b , c ); 1 μm ( d , e , g , h ); 0.5 μm and 2.5 s ( i ).

Article Snippet: For NLS-TagBFP expression (Fig. ), a construct encoding a nuclear localization sequence (NLS) followed by TagBFP was synthethized by Twist Bioscience and cloned into a plasmid containing a cytomegalovirus promoter.

Techniques: Imaging, Expressing

Journal: eLife

Article Title: Small-molecule G-quadruplex stabilizers reveal a novel pathway of autophagy regulation in neurons

doi: 10.7554/eLife.52283

Figure Lengend Snippet:

Article Snippet: Recombinant DNA reagent , pCAG-TagBFP , VectorBuilder , pRP[Exp]-CAG > TagBFP , .

Techniques: Isolation, Recombinant, Clone Assay, Construct, Sequencing, Synthesized, Software