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gfp mapper  (Addgene inc)


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    Structured Review

    Addgene inc gfp mapper
    Gfp Mapper, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gfp-sec61b/mCherry-Sec61b-C1+(Plasmid+%2390994)/pm41844235-220-12-13
    Average 93 stars, based on 15 article reviews
    gfp mapper - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Transfection:

    Article Title: Smart lattice light-sheet microscopy for imaging rare and complex cellular events.
    Article Snippet: On the day of transfection, three distinct DNA plasmid solutions were prepared in Opti-MEM (Thermo Fisher Scientific, 31985070): one with 100 ng of GFP-Sec61b (Addgene Plasmid, 121159), another with 100 ng of HaloTag-Tomm20 (Addgene Plasmid,123284) and a third mixture containing 100 ng each of GFP-Sec61b and HaloTag-Tomm20.

    Article Title: Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactions
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Catalase Sigma-Aldrich C40 Acryloyl-X-SE Thermo Fisher Scientific A20770 Acrylamide 40% Sigma-Aldrich A4058 N,N0-Methylenebisacrylamide Sigma-Aldrich M1533 Sodium acrylate Sigma-Aldrich 408220 TEMED Bio-Rad 1610800 APS Sigma-Aldrich A3678 anhydrous-DMSO Thermo Fisher Scientific D12345 Guanidine HCl Sigma-Aldrich G3272 Triton-X-100 Sigma-Aldrich 93433 Proteinase K Thermo Fisher Scientific EO0492 0.1% (w/v) poly-L-lysine Sigma-Aldrich P8920 Deposited data Proteomics data P180 pulldown This study PXD050948 RNA-sequencing data P180 This study GSE262262 Experimental models: Cell lines HEK-293T ATCC CRL-3216 Experimental models: Organisms/strains Rat (Wistar) Janvier N/A Recombinant DNA pSuper Brummelkamp et al.74 N/A pGW1-mCherry Kapitein et al.75 N/A pGW1-BFP Kapitein et al.75 N/A RTN4A-GFP Kind gift from dr. Voeltz (Howard Hughes Medical Institute & Department of Molecular, Cellular and Developmental Biology, University of Colorado) Addgene #61807 pEGFP(A206K)-N1 Kind gift from dr. Lippincott-Schwartz- (Howard Hughes Medical Institute, Janelia Research Campus) N/A pEGFP(A206K)-C1 Kind gift from dr. Lippincott-Schwartz (Howard Hughes Medical Institute, Janelia Research Campus) N/A GFP-Sec61b Kind gift from dr. Rapaport (Department of Cell Biology, Harvard Medical School) Addgene #15108 DP1-GFP Farı́as et al.12 N/A RpL10A-tagRFP Kind gift from dr. Singer (Department of Cell Biology, Albert Einstein College of Medicine) Addgene #74172 TOM20-V5-FKBP-AP Kind gift from dr. Ting (Department of Genetics& Biology, Stanford University) Addgene #120914 mCherrymyr5’/3’-Calreticulin Kind gift from dr. Twiss (Department Biological Sciences, University of South Carolina) N/A Lifeact-mCherry Kind gift from dr. Sato (Graduate School of Arts and Sciences, University of Tokyo) Addgene #67302 HA-KifC1-MD-Strep Farı́as et al.12 N/A GFP-SBP-RTN4A Farı́as et al.12 N/A P180-DCoiled-coil-GFP Farı́as et al.12 N/A P180-DCoiled-coil-GFPAviTag This study N/A P180-Drepeats-GFP Farı́as et al.12 N/A P180-Drepeats-GFPAviTag This study N/A P180-Coiled-coil-GFPAviTag This study N/A P180-Repeats-GFPAviTag This study N/A SplitAP-V5-C1 Özkan et al.19 N/A (Continued on next page) ll OPEN ACCESS Article e2 Developmental Cell 59, 2053–2068.e1–e9, August 19, 2024

    Plasmid Preparation:

    Article Title: Smart lattice light-sheet microscopy for imaging rare and complex cellular events.
    Article Snippet: On the day of transfection, three distinct DNA plasmid solutions were prepared in Opti-MEM (Thermo Fisher Scientific, 31985070): one with 100 ng of GFP-Sec61b (Addgene Plasmid, 121159), another with 100 ng of HaloTag-Tomm20 (Addgene Plasmid,123284) and a third mixture containing 100 ng each of GFP-Sec61b and HaloTag-Tomm20.

    Article Title: Axonal endoplasmic reticulum tubules control local translation via P180/RRBP1-mediated ribosome interactions
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Catalase Sigma-Aldrich C40 Acryloyl-X-SE Thermo Fisher Scientific A20770 Acrylamide 40% Sigma-Aldrich A4058 N,N0-Methylenebisacrylamide Sigma-Aldrich M1533 Sodium acrylate Sigma-Aldrich 408220 TEMED Bio-Rad 1610800 APS Sigma-Aldrich A3678 anhydrous-DMSO Thermo Fisher Scientific D12345 Guanidine HCl Sigma-Aldrich G3272 Triton-X-100 Sigma-Aldrich 93433 Proteinase K Thermo Fisher Scientific EO0492 0.1% (w/v) poly-L-lysine Sigma-Aldrich P8920 Deposited data Proteomics data P180 pulldown This study PXD050948 RNA-sequencing data P180 This study GSE262262 Experimental models: Cell lines HEK-293T ATCC CRL-3216 Experimental models: Organisms/strains Rat (Wistar) Janvier N/A Recombinant DNA pSuper Brummelkamp et al.74 N/A pGW1-mCherry Kapitein et al.75 N/A pGW1-BFP Kapitein et al.75 N/A RTN4A-GFP Kind gift from dr. Voeltz (Howard Hughes Medical Institute & Department of Molecular, Cellular and Developmental Biology, University of Colorado) Addgene #61807 pEGFP(A206K)-N1 Kind gift from dr. Lippincott-Schwartz- (Howard Hughes Medical Institute, Janelia Research Campus) N/A pEGFP(A206K)-C1 Kind gift from dr. Lippincott-Schwartz (Howard Hughes Medical Institute, Janelia Research Campus) N/A GFP-Sec61b Kind gift from dr. Rapaport (Department of Cell Biology, Harvard Medical School) Addgene #15108 DP1-GFP Farı́as et al.12 N/A RpL10A-tagRFP Kind gift from dr. Singer (Department of Cell Biology, Albert Einstein College of Medicine) Addgene #74172 TOM20-V5-FKBP-AP Kind gift from dr. Ting (Department of Genetics& Biology, Stanford University) Addgene #120914 mCherrymyr5’/3’-Calreticulin Kind gift from dr. Twiss (Department Biological Sciences, University of South Carolina) N/A Lifeact-mCherry Kind gift from dr. Sato (Graduate School of Arts and Sciences, University of Tokyo) Addgene #67302 HA-KifC1-MD-Strep Farı́as et al.12 N/A GFP-SBP-RTN4A Farı́as et al.12 N/A P180-DCoiled-coil-GFP Farı́as et al.12 N/A P180-DCoiled-coil-GFPAviTag This study N/A P180-Drepeats-GFP Farı́as et al.12 N/A P180-Drepeats-GFPAviTag This study N/A P180-Coiled-coil-GFPAviTag This study N/A P180-Repeats-GFPAviTag This study N/A SplitAP-V5-C1 Özkan et al.19 N/A (Continued on next page) ll OPEN ACCESS Article e2 Developmental Cell 59, 2053–2068.e1–e9, August 19, 2024



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    Addgene inc gfp mapper
    Gfp Mapper, supplied by Addgene inc, 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/product/gfp-sec61b/mCherry-Sec61b-C1+(Plasmid+%2390994)/pm41844235-220-12-13
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    Addgene inc gfp
    a Time-averaged TIRF images of a Hela cell expressing <t>a</t> <t>SEC61B::GFP</t> ER marker (grayscale) with knock-in SEC13::SNAP (stained with cpSNAP-JF549) ER exit site marker (cyan). b Reconstructed Halo ER (ER-targeted HaloTag with KDEL retention signal, stained with PA-JF646) trajectories (individually colour-coded) reconstructed without (left) or with FidlTrack (right). c Percentage of ambiguous displacements for the trajectories reconstructed without or with FidlTrack. d Trajectories (individually colour-coded) visiting an ERES (spending at least 10 frames in ERES) found without (left) or with FidlTrack (right) overlaid on top of the averaged ER structure (grayscale) and ERES positions (cyan). e Blow up on the two regions highlighted in ( d ) showing how ERES act as attractors to local trajectories without FidlTrack (left), a problem mostly corrected when using FidlTrack (right). f Number of trajectories at ERES (spending at least 2 points close to an ERES) without and with FidlTrack. g , Average amount of time spent by trajectories close to ERES versus close to random ERES-like sites (see Fig. ). h Amount of the time spent in ERES by trajectories spending at least 5 frames at an ERES with a cutoff at 500 ms. The red line corresponds to a fit of the distribution to a biexponential function of parameters \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$a=156$$\end{document} a = 156 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 1=10$$\end{document} τ 1 = 10 ms, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$b=29$$\end{document} b = 29 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 2=56$$\end{document} τ 2 = 56 ms and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${R}^{2}=0.997$$\end{document} R 2 = 0.997 . i Example of a trajectory flying-by (passing without stopping) an ERES (left) and quantification of its distance to the ERES (right, top) and instantaneous displacement length (right, bottom) showing no sign of association with the ERES. j Same as ( i ) but for a trajectory visiting for some frames and then exiting an ERES. k Same as ( j ) but for a trajectory dwelling for a long time in an ERES (until bleaching). l Ratio of visiting to flyby trajectories per exit site. m Exit sites colour-coded by their visiting to flyby trajectory ratio as presented in ( l ). n Example of two exit sites exhibiting different behaviours, the left one is “sticky” with a high ratio of visiting trajectories while the right one has mostly flyby trajectories. Source data are provided as a Source Data file.
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    Addgene inc pcdna3 1 gfp sec61b sec61b
    a Time-averaged TIRF images of a Hela cell expressing <t>a</t> <t>SEC61B::GFP</t> ER marker (grayscale) with knock-in SEC13::SNAP (stained with cpSNAP-JF549) ER exit site marker (cyan). b Reconstructed Halo ER (ER-targeted HaloTag with KDEL retention signal, stained with PA-JF646) trajectories (individually colour-coded) reconstructed without (left) or with FidlTrack (right). c Percentage of ambiguous displacements for the trajectories reconstructed without or with FidlTrack. d Trajectories (individually colour-coded) visiting an ERES (spending at least 10 frames in ERES) found without (left) or with FidlTrack (right) overlaid on top of the averaged ER structure (grayscale) and ERES positions (cyan). e Blow up on the two regions highlighted in ( d ) showing how ERES act as attractors to local trajectories without FidlTrack (left), a problem mostly corrected when using FidlTrack (right). f Number of trajectories at ERES (spending at least 2 points close to an ERES) without and with FidlTrack. g , Average amount of time spent by trajectories close to ERES versus close to random ERES-like sites (see Fig. ). h Amount of the time spent in ERES by trajectories spending at least 5 frames at an ERES with a cutoff at 500 ms. The red line corresponds to a fit of the distribution to a biexponential function of parameters \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$a=156$$\end{document} a = 156 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 1=10$$\end{document} τ 1 = 10 ms, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$b=29$$\end{document} b = 29 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 2=56$$\end{document} τ 2 = 56 ms and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${R}^{2}=0.997$$\end{document} R 2 = 0.997 . i Example of a trajectory flying-by (passing without stopping) an ERES (left) and quantification of its distance to the ERES (right, top) and instantaneous displacement length (right, bottom) showing no sign of association with the ERES. j Same as ( i ) but for a trajectory visiting for some frames and then exiting an ERES. k Same as ( j ) but for a trajectory dwelling for a long time in an ERES (until bleaching). l Ratio of visiting to flyby trajectories per exit site. m Exit sites colour-coded by their visiting to flyby trajectory ratio as presented in ( l ). n Example of two exit sites exhibiting different behaviours, the left one is “sticky” with a high ratio of visiting trajectories while the right one has mostly flyby trajectories. Source data are provided as a Source Data file.
    Pcdna3 1 Gfp Sec61b Sec61b, supplied by Addgene inc, 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/product/gfp-sec61b/GFP-+SEC61B+(Plasmid+%23121159)/pm41672994-534-184-193
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    Addgene inc pcdna3 1 gfp sec61b
    a Time-averaged TIRF images of a Hela cell expressing <t>a</t> <t>SEC61B::GFP</t> ER marker (grayscale) with knock-in SEC13::SNAP (stained with cpSNAP-JF549) ER exit site marker (cyan). b Reconstructed Halo ER (ER-targeted HaloTag with KDEL retention signal, stained with PA-JF646) trajectories (individually colour-coded) reconstructed without (left) or with FidlTrack (right). c Percentage of ambiguous displacements for the trajectories reconstructed without or with FidlTrack. d Trajectories (individually colour-coded) visiting an ERES (spending at least 10 frames in ERES) found without (left) or with FidlTrack (right) overlaid on top of the averaged ER structure (grayscale) and ERES positions (cyan). e Blow up on the two regions highlighted in ( d ) showing how ERES act as attractors to local trajectories without FidlTrack (left), a problem mostly corrected when using FidlTrack (right). f Number of trajectories at ERES (spending at least 2 points close to an ERES) without and with FidlTrack. g , Average amount of time spent by trajectories close to ERES versus close to random ERES-like sites (see Fig. ). h Amount of the time spent in ERES by trajectories spending at least 5 frames at an ERES with a cutoff at 500 ms. The red line corresponds to a fit of the distribution to a biexponential function of parameters \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$a=156$$\end{document} a = 156 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 1=10$$\end{document} τ 1 = 10 ms, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$b=29$$\end{document} b = 29 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 2=56$$\end{document} τ 2 = 56 ms and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${R}^{2}=0.997$$\end{document} R 2 = 0.997 . i Example of a trajectory flying-by (passing without stopping) an ERES (left) and quantification of its distance to the ERES (right, top) and instantaneous displacement length (right, bottom) showing no sign of association with the ERES. j Same as ( i ) but for a trajectory visiting for some frames and then exiting an ERES. k Same as ( j ) but for a trajectory dwelling for a long time in an ERES (until bleaching). l Ratio of visiting to flyby trajectories per exit site. m Exit sites colour-coded by their visiting to flyby trajectory ratio as presented in ( l ). n Example of two exit sites exhibiting different behaviours, the left one is “sticky” with a high ratio of visiting trajectories while the right one has mostly flyby trajectories. Source data are provided as a Source Data file.
    Pcdna3 1 Gfp Sec61b, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Addgene inc gfp sec61b
    a Time-averaged TIRF images of a Hela cell expressing <t>a</t> <t>SEC61B::GFP</t> ER marker (grayscale) with knock-in SEC13::SNAP (stained with cpSNAP-JF549) ER exit site marker (cyan). b Reconstructed Halo ER (ER-targeted HaloTag with KDEL retention signal, stained with PA-JF646) trajectories (individually colour-coded) reconstructed without (left) or with FidlTrack (right). c Percentage of ambiguous displacements for the trajectories reconstructed without or with FidlTrack. d Trajectories (individually colour-coded) visiting an ERES (spending at least 10 frames in ERES) found without (left) or with FidlTrack (right) overlaid on top of the averaged ER structure (grayscale) and ERES positions (cyan). e Blow up on the two regions highlighted in ( d ) showing how ERES act as attractors to local trajectories without FidlTrack (left), a problem mostly corrected when using FidlTrack (right). f Number of trajectories at ERES (spending at least 2 points close to an ERES) without and with FidlTrack. g , Average amount of time spent by trajectories close to ERES versus close to random ERES-like sites (see Fig. ). h Amount of the time spent in ERES by trajectories spending at least 5 frames at an ERES with a cutoff at 500 ms. The red line corresponds to a fit of the distribution to a biexponential function of parameters \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$a=156$$\end{document} a = 156 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 1=10$$\end{document} τ 1 = 10 ms, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$b=29$$\end{document} b = 29 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 2=56$$\end{document} τ 2 = 56 ms and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${R}^{2}=0.997$$\end{document} R 2 = 0.997 . i Example of a trajectory flying-by (passing without stopping) an ERES (left) and quantification of its distance to the ERES (right, top) and instantaneous displacement length (right, bottom) showing no sign of association with the ERES. j Same as ( i ) but for a trajectory visiting for some frames and then exiting an ERES. k Same as ( j ) but for a trajectory dwelling for a long time in an ERES (until bleaching). l Ratio of visiting to flyby trajectories per exit site. m Exit sites colour-coded by their visiting to flyby trajectory ratio as presented in ( l ). n Example of two exit sites exhibiting different behaviours, the left one is “sticky” with a high ratio of visiting trajectories while the right one has mostly flyby trajectories. Source data are provided as a Source Data file.
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    Addgene inc sec61b
    a TIRF images of a frame from simultaneously acquired single-molecules (left) and the associated organelle geometries (right) for a mitochondria matrix targeted HaloTag probe and mNeonGreen marker (top), the mitochondria membrane protein TOMM20 and mitochondria matrix targeted mEmerald (middle), and the ER membrane protein <t>SEC61B</t> and ER lumen targeted mEmerald (bottom) in COS-7 cells. b Masks extracted via AI-assisted image processing from the first and last frame of the recordings for the mitochondria matrix targeted probe (top), TOMM20 (middle) and SEC61B (bottom) recordings presented in ( a ). c Stability maps, representing for each pixel the percentage of total frames in which it is part of a mask, for the mitochondria matrix targeted probe (top), TOMM20 (middle) and SEC61B (bottom) recordings presented in ( a ). d Bar plot presenting the fraction of recovered spots relative to the quantity recovered from the entire stack of masks when using the mask of either the first or last frame to perform structure-aware tracking in the different recordings presented in ( a ). e Reconstructed trajectories (individually colour-coded) from the datasets presented in ( a ) using conventional tracking (not structure-aware, top, left), structure-aware tracking using the mask from the first frame (top, right) or the whole stack of masks (bottom, left). f Plot of the displacement distributions extracted from the trajectories presented in ( e ) fitted to a mixture of two Rayleigh distributions (dashed red lines, see Methods section “Fitting of displacement lengths distributions”). g Plot of the pooled displacement distributions for structure-aware ambiguity-removed tracking of SEC61B::Halotag in COS-7 cells after 4 h of BSA or Oleic Acid treatment at 400 µM. Pooling was done over n =7/6 recordings for BSA and oleic acid, respectively, the reported statistics correspond to a two-tailed Kolmogorov–Smirnov test p < 2.2251e-308. h Bar plot of the Kolmogorov–Smirnov statistics from ( g ) for either conventional or structure-aware tracking and with or without ambiguity removal. i Temporally colour-coded mitochondria positions over 700 frames (left), trajectory of the centre of the pointed mitochondria (right, top) and the raw (black) and mitochondrion motion-corrected trajectory (red) of a TOMM20 receptor moving at the surface of the pointed mitochondrion (right, bottom). Source data are provided as a Source Data file.
    Sec61b, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Addgene inc christine mayr
    a TIRF images of a frame from simultaneously acquired single-molecules (left) and the associated organelle geometries (right) for a mitochondria matrix targeted HaloTag probe and mNeonGreen marker (top), the mitochondria membrane protein TOMM20 and mitochondria matrix targeted mEmerald (middle), and the ER membrane protein <t>SEC61B</t> and ER lumen targeted mEmerald (bottom) in COS-7 cells. b Masks extracted via AI-assisted image processing from the first and last frame of the recordings for the mitochondria matrix targeted probe (top), TOMM20 (middle) and SEC61B (bottom) recordings presented in ( a ). c Stability maps, representing for each pixel the percentage of total frames in which it is part of a mask, for the mitochondria matrix targeted probe (top), TOMM20 (middle) and SEC61B (bottom) recordings presented in ( a ). d Bar plot presenting the fraction of recovered spots relative to the quantity recovered from the entire stack of masks when using the mask of either the first or last frame to perform structure-aware tracking in the different recordings presented in ( a ). e Reconstructed trajectories (individually colour-coded) from the datasets presented in ( a ) using conventional tracking (not structure-aware, top, left), structure-aware tracking using the mask from the first frame (top, right) or the whole stack of masks (bottom, left). f Plot of the displacement distributions extracted from the trajectories presented in ( e ) fitted to a mixture of two Rayleigh distributions (dashed red lines, see Methods section “Fitting of displacement lengths distributions”). g Plot of the pooled displacement distributions for structure-aware ambiguity-removed tracking of SEC61B::Halotag in COS-7 cells after 4 h of BSA or Oleic Acid treatment at 400 µM. Pooling was done over n =7/6 recordings for BSA and oleic acid, respectively, the reported statistics correspond to a two-tailed Kolmogorov–Smirnov test p < 2.2251e-308. h Bar plot of the Kolmogorov–Smirnov statistics from ( g ) for either conventional or structure-aware tracking and with or without ambiguity removal. i Temporally colour-coded mitochondria positions over 700 frames (left), trajectory of the centre of the pointed mitochondria (right, top) and the raw (black) and mitochondrion motion-corrected trajectory (red) of a TOMM20 receptor moving at the surface of the pointed mitochondrion (right, bottom). Source data are provided as a Source Data file.
    Christine Mayr, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    a Time-averaged TIRF images of a Hela cell expressing a SEC61B::GFP ER marker (grayscale) with knock-in SEC13::SNAP (stained with cpSNAP-JF549) ER exit site marker (cyan). b Reconstructed Halo ER (ER-targeted HaloTag with KDEL retention signal, stained with PA-JF646) trajectories (individually colour-coded) reconstructed without (left) or with FidlTrack (right). c Percentage of ambiguous displacements for the trajectories reconstructed without or with FidlTrack. d Trajectories (individually colour-coded) visiting an ERES (spending at least 10 frames in ERES) found without (left) or with FidlTrack (right) overlaid on top of the averaged ER structure (grayscale) and ERES positions (cyan). e Blow up on the two regions highlighted in ( d ) showing how ERES act as attractors to local trajectories without FidlTrack (left), a problem mostly corrected when using FidlTrack (right). f Number of trajectories at ERES (spending at least 2 points close to an ERES) without and with FidlTrack. g , Average amount of time spent by trajectories close to ERES versus close to random ERES-like sites (see Fig. ). h Amount of the time spent in ERES by trajectories spending at least 5 frames at an ERES with a cutoff at 500 ms. The red line corresponds to a fit of the distribution to a biexponential function of parameters \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$a=156$$\end{document} a = 156 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 1=10$$\end{document} τ 1 = 10 ms, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$b=29$$\end{document} b = 29 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 2=56$$\end{document} τ 2 = 56 ms and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${R}^{2}=0.997$$\end{document} R 2 = 0.997 . i Example of a trajectory flying-by (passing without stopping) an ERES (left) and quantification of its distance to the ERES (right, top) and instantaneous displacement length (right, bottom) showing no sign of association with the ERES. j Same as ( i ) but for a trajectory visiting for some frames and then exiting an ERES. k Same as ( j ) but for a trajectory dwelling for a long time in an ERES (until bleaching). l Ratio of visiting to flyby trajectories per exit site. m Exit sites colour-coded by their visiting to flyby trajectory ratio as presented in ( l ). n Example of two exit sites exhibiting different behaviours, the left one is “sticky” with a high ratio of visiting trajectories while the right one has mostly flyby trajectories. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: FidlTrack: high-fidelity structure-aware single particle tracking resolves intracellular molecular motion in organelles sensing APP processing

    doi: 10.1038/s41467-026-69067-y

    Figure Lengend Snippet: a Time-averaged TIRF images of a Hela cell expressing a SEC61B::GFP ER marker (grayscale) with knock-in SEC13::SNAP (stained with cpSNAP-JF549) ER exit site marker (cyan). b Reconstructed Halo ER (ER-targeted HaloTag with KDEL retention signal, stained with PA-JF646) trajectories (individually colour-coded) reconstructed without (left) or with FidlTrack (right). c Percentage of ambiguous displacements for the trajectories reconstructed without or with FidlTrack. d Trajectories (individually colour-coded) visiting an ERES (spending at least 10 frames in ERES) found without (left) or with FidlTrack (right) overlaid on top of the averaged ER structure (grayscale) and ERES positions (cyan). e Blow up on the two regions highlighted in ( d ) showing how ERES act as attractors to local trajectories without FidlTrack (left), a problem mostly corrected when using FidlTrack (right). f Number of trajectories at ERES (spending at least 2 points close to an ERES) without and with FidlTrack. g , Average amount of time spent by trajectories close to ERES versus close to random ERES-like sites (see Fig. ). h Amount of the time spent in ERES by trajectories spending at least 5 frames at an ERES with a cutoff at 500 ms. The red line corresponds to a fit of the distribution to a biexponential function of parameters \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$a=156$$\end{document} a = 156 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 1=10$$\end{document} τ 1 = 10 ms, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$b=29$$\end{document} b = 29 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 2=56$$\end{document} τ 2 = 56 ms and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${R}^{2}=0.997$$\end{document} R 2 = 0.997 . i Example of a trajectory flying-by (passing without stopping) an ERES (left) and quantification of its distance to the ERES (right, top) and instantaneous displacement length (right, bottom) showing no sign of association with the ERES. j Same as ( i ) but for a trajectory visiting for some frames and then exiting an ERES. k Same as ( j ) but for a trajectory dwelling for a long time in an ERES (until bleaching). l Ratio of visiting to flyby trajectories per exit site. m Exit sites colour-coded by their visiting to flyby trajectory ratio as presented in ( l ). n Example of two exit sites exhibiting different behaviours, the left one is “sticky” with a high ratio of visiting trajectories while the right one has mostly flyby trajectories. Source data are provided as a Source Data file.

    Article Snippet: 1014 , pcDNA3.1_GFP-SEC61B , SEC61B:: GFP , SEC61B fused to GFP , Fig. , Addgene #121159.

    Techniques: Expressing, Marker, Knock-In, Staining

    a TIRF images of a frame from simultaneously acquired single-molecules (left) and the associated organelle geometries (right) for a mitochondria matrix targeted HaloTag probe and mNeonGreen marker (top), the mitochondria membrane protein TOMM20 and mitochondria matrix targeted mEmerald (middle), and the ER membrane protein SEC61B and ER lumen targeted mEmerald (bottom) in COS-7 cells. b Masks extracted via AI-assisted image processing from the first and last frame of the recordings for the mitochondria matrix targeted probe (top), TOMM20 (middle) and SEC61B (bottom) recordings presented in ( a ). c Stability maps, representing for each pixel the percentage of total frames in which it is part of a mask, for the mitochondria matrix targeted probe (top), TOMM20 (middle) and SEC61B (bottom) recordings presented in ( a ). d Bar plot presenting the fraction of recovered spots relative to the quantity recovered from the entire stack of masks when using the mask of either the first or last frame to perform structure-aware tracking in the different recordings presented in ( a ). e Reconstructed trajectories (individually colour-coded) from the datasets presented in ( a ) using conventional tracking (not structure-aware, top, left), structure-aware tracking using the mask from the first frame (top, right) or the whole stack of masks (bottom, left). f Plot of the displacement distributions extracted from the trajectories presented in ( e ) fitted to a mixture of two Rayleigh distributions (dashed red lines, see Methods section “Fitting of displacement lengths distributions”). g Plot of the pooled displacement distributions for structure-aware ambiguity-removed tracking of SEC61B::Halotag in COS-7 cells after 4 h of BSA or Oleic Acid treatment at 400 µM. Pooling was done over n =7/6 recordings for BSA and oleic acid, respectively, the reported statistics correspond to a two-tailed Kolmogorov–Smirnov test p < 2.2251e-308. h Bar plot of the Kolmogorov–Smirnov statistics from ( g ) for either conventional or structure-aware tracking and with or without ambiguity removal. i Temporally colour-coded mitochondria positions over 700 frames (left), trajectory of the centre of the pointed mitochondria (right, top) and the raw (black) and mitochondrion motion-corrected trajectory (red) of a TOMM20 receptor moving at the surface of the pointed mitochondrion (right, bottom). Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: FidlTrack: high-fidelity structure-aware single particle tracking resolves intracellular molecular motion in organelles sensing APP processing

    doi: 10.1038/s41467-026-69067-y

    Figure Lengend Snippet: a TIRF images of a frame from simultaneously acquired single-molecules (left) and the associated organelle geometries (right) for a mitochondria matrix targeted HaloTag probe and mNeonGreen marker (top), the mitochondria membrane protein TOMM20 and mitochondria matrix targeted mEmerald (middle), and the ER membrane protein SEC61B and ER lumen targeted mEmerald (bottom) in COS-7 cells. b Masks extracted via AI-assisted image processing from the first and last frame of the recordings for the mitochondria matrix targeted probe (top), TOMM20 (middle) and SEC61B (bottom) recordings presented in ( a ). c Stability maps, representing for each pixel the percentage of total frames in which it is part of a mask, for the mitochondria matrix targeted probe (top), TOMM20 (middle) and SEC61B (bottom) recordings presented in ( a ). d Bar plot presenting the fraction of recovered spots relative to the quantity recovered from the entire stack of masks when using the mask of either the first or last frame to perform structure-aware tracking in the different recordings presented in ( a ). e Reconstructed trajectories (individually colour-coded) from the datasets presented in ( a ) using conventional tracking (not structure-aware, top, left), structure-aware tracking using the mask from the first frame (top, right) or the whole stack of masks (bottom, left). f Plot of the displacement distributions extracted from the trajectories presented in ( e ) fitted to a mixture of two Rayleigh distributions (dashed red lines, see Methods section “Fitting of displacement lengths distributions”). g Plot of the pooled displacement distributions for structure-aware ambiguity-removed tracking of SEC61B::Halotag in COS-7 cells after 4 h of BSA or Oleic Acid treatment at 400 µM. Pooling was done over n =7/6 recordings for BSA and oleic acid, respectively, the reported statistics correspond to a two-tailed Kolmogorov–Smirnov test p < 2.2251e-308. h Bar plot of the Kolmogorov–Smirnov statistics from ( g ) for either conventional or structure-aware tracking and with or without ambiguity removal. i Temporally colour-coded mitochondria positions over 700 frames (left), trajectory of the centre of the pointed mitochondria (right, top) and the raw (black) and mitochondrion motion-corrected trajectory (red) of a TOMM20 receptor moving at the surface of the pointed mitochondrion (right, bottom). Source data are provided as a Source Data file.

    Article Snippet: 1014 , pcDNA3.1_GFP-SEC61B , SEC61B:: GFP , SEC61B fused to GFP , Fig. , Addgene #121159.

    Techniques: Marker, Membrane, Two Tailed Test

    a Time-averaged TIRF images of a Hela cell expressing a SEC61B::GFP ER marker (grayscale) with knock-in SEC13::SNAP (stained with cpSNAP-JF549) ER exit site marker (cyan). b Reconstructed Halo ER (ER-targeted HaloTag with KDEL retention signal, stained with PA-JF646) trajectories (individually colour-coded) reconstructed without (left) or with FidlTrack (right). c Percentage of ambiguous displacements for the trajectories reconstructed without or with FidlTrack. d Trajectories (individually colour-coded) visiting an ERES (spending at least 10 frames in ERES) found without (left) or with FidlTrack (right) overlaid on top of the averaged ER structure (grayscale) and ERES positions (cyan). e Blow up on the two regions highlighted in ( d ) showing how ERES act as attractors to local trajectories without FidlTrack (left), a problem mostly corrected when using FidlTrack (right). f Number of trajectories at ERES (spending at least 2 points close to an ERES) without and with FidlTrack. g , Average amount of time spent by trajectories close to ERES versus close to random ERES-like sites (see Fig. ). h Amount of the time spent in ERES by trajectories spending at least 5 frames at an ERES with a cutoff at 500 ms. The red line corresponds to a fit of the distribution to a biexponential function of parameters \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$a=156$$\end{document} a = 156 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 1=10$$\end{document} τ 1 = 10 ms, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$b=29$$\end{document} b = 29 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 2=56$$\end{document} τ 2 = 56 ms and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${R}^{2}=0.997$$\end{document} R 2 = 0.997 . i Example of a trajectory flying-by (passing without stopping) an ERES (left) and quantification of its distance to the ERES (right, top) and instantaneous displacement length (right, bottom) showing no sign of association with the ERES. j Same as ( i ) but for a trajectory visiting for some frames and then exiting an ERES. k Same as ( j ) but for a trajectory dwelling for a long time in an ERES (until bleaching). l Ratio of visiting to flyby trajectories per exit site. m Exit sites colour-coded by their visiting to flyby trajectory ratio as presented in ( l ). n Example of two exit sites exhibiting different behaviours, the left one is “sticky” with a high ratio of visiting trajectories while the right one has mostly flyby trajectories. Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: FidlTrack: high-fidelity structure-aware single particle tracking resolves intracellular molecular motion in organelles sensing APP processing

    doi: 10.1038/s41467-026-69067-y

    Figure Lengend Snippet: a Time-averaged TIRF images of a Hela cell expressing a SEC61B::GFP ER marker (grayscale) with knock-in SEC13::SNAP (stained with cpSNAP-JF549) ER exit site marker (cyan). b Reconstructed Halo ER (ER-targeted HaloTag with KDEL retention signal, stained with PA-JF646) trajectories (individually colour-coded) reconstructed without (left) or with FidlTrack (right). c Percentage of ambiguous displacements for the trajectories reconstructed without or with FidlTrack. d Trajectories (individually colour-coded) visiting an ERES (spending at least 10 frames in ERES) found without (left) or with FidlTrack (right) overlaid on top of the averaged ER structure (grayscale) and ERES positions (cyan). e Blow up on the two regions highlighted in ( d ) showing how ERES act as attractors to local trajectories without FidlTrack (left), a problem mostly corrected when using FidlTrack (right). f Number of trajectories at ERES (spending at least 2 points close to an ERES) without and with FidlTrack. g , Average amount of time spent by trajectories close to ERES versus close to random ERES-like sites (see Fig. ). h Amount of the time spent in ERES by trajectories spending at least 5 frames at an ERES with a cutoff at 500 ms. The red line corresponds to a fit of the distribution to a biexponential function of parameters \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$a=156$$\end{document} a = 156 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 1=10$$\end{document} τ 1 = 10 ms, \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$b=29$$\end{document} b = 29 , \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$$\tau 2=56$$\end{document} τ 2 = 56 ms and \documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${R}^{2}=0.997$$\end{document} R 2 = 0.997 . i Example of a trajectory flying-by (passing without stopping) an ERES (left) and quantification of its distance to the ERES (right, top) and instantaneous displacement length (right, bottom) showing no sign of association with the ERES. j Same as ( i ) but for a trajectory visiting for some frames and then exiting an ERES. k Same as ( j ) but for a trajectory dwelling for a long time in an ERES (until bleaching). l Ratio of visiting to flyby trajectories per exit site. m Exit sites colour-coded by their visiting to flyby trajectory ratio as presented in ( l ). n Example of two exit sites exhibiting different behaviours, the left one is “sticky” with a high ratio of visiting trajectories while the right one has mostly flyby trajectories. Source data are provided as a Source Data file.

    Article Snippet: 1014 , pcDNA3.1_GFP-SEC61B , SEC61B:: GFP , SEC61B fused to GFP , Fig. , Addgene #121159.

    Techniques: Expressing, Marker, Knock-In, Staining