flexi trace software Search Results


aav1 syn flex tva 2a egfp 2a rvg unc vector core addgene  (Addgene inc)
93
Addgene inc aav1 syn flex tva 2a egfp 2a rvg unc vector core addgene
(A) Diagram of monosynaptic retrograde tracing assay using EnvA-coated G-deleted rabies virus expressing mCherry (EnvA-SADΔG-mcherry). G and <t>TVA</t> proteins were expressed in specific INs by the use of Cre mice together with <t>AAV1-FLEX-TVA-2A-EGFP-2A-RVG</t> (for Chx10+ and Vglut3+ INs) or lox-stop-lox-histone GFP-2A-TVA-2A-RVG mice (for Ptf1a+ INs). (B–D) Representative images of CSNs traced from Chx10+ (B), Ptf1a+ (C), and Vglut3+ (D) INs. In the panels, two images were combined to cover medial and laterals region of the cortex. White dotted lines show the cerebral cortex margins. Coronal section: right, medial; left, lateral. Scale bar, 100 μm. (E) Plotting of EnvA-SADΔG-mCherry+ CSNs traced from Chx10+ (red), Ptf1a+ (green), and Vglut3+ (blue) INs. Top view of the cortex. (F) Ratios of EnvA-SADΔG-mCherry+ CSNs traced from Chx10+ (red), Ptf1a+ (green), and Vglut3+ (blue) INs in ML % 1.7 mm, 1.7–2.0 mm, and R2.0 mm to total labeled neurons. Data are represented as mean ± SEM (n = 3). See also Figure S4.
Aav1 Syn Flex Tva 2a Egfp 2a Rvg Unc Vector Core Addgene, 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/result/aav1 syn flex tva 2a egfp 2a rvg unc vector core addgene/product/Addgene inc
Average 93 stars, based on 1 article reviews
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3d motion capture system  (Leyard Optoelectronic)
86
Leyard Optoelectronic 3d motion capture system
a , Module crosscorrelograms for sessions in different rooms (A1×B1) at incremental degrees of rotation in rat #26718 (select number of rotations shown here for visualization purposes; see for additional rotations) (as in , right). Asterisks denote overall maximum for each module. b , Maximum correlation between <t>3D</t> stacks of rate maps of sessions A1 and B1 (with cell identity along the z-axis) as a function of rotation for each module in rat #26718. Maximum correlation refers to the highest value within the crosscorrelation matrix at each rotation. Note that the rotation was nearly identical across modules. c , Rotation of each simultaneously recorded module between sessions (38 session pairs in 10 rats, as in ). Lines connect data from a single recording. A fourth module was recorded in 4 session pairs. Its rotation did not differ from the other simultaneously recorded modules . d , Difference in rotation between simultaneously recorded module pairs (n = 104 module pairs, each pair indicated by a circle). Red crosses indicate medians. Dashed gray line at 90° represents chance. e , Gray lines show coherent rotation between sessions for grid, head direction (HD), and border cells (n = 22 experiments). Lines connect data from a single recording.
3d Motion Capture System, supplied by Leyard Optoelectronic, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/3d motion capture system/product/Leyard Optoelectronic
Average 86 stars, based on 1 article reviews
3d motion capture system - by Bioz Stars, 2026-06
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edf trace v 1.0 software  (Marburg GmbH)
90
Marburg GmbH edf trace v 1.0 software
a , Module crosscorrelograms for sessions in different rooms (A1×B1) at incremental degrees of rotation in rat #26718 (select number of rotations shown here for visualization purposes; see for additional rotations) (as in , right). Asterisks denote overall maximum for each module. b , Maximum correlation between <t>3D</t> stacks of rate maps of sessions A1 and B1 (with cell identity along the z-axis) as a function of rotation for each module in rat #26718. Maximum correlation refers to the highest value within the crosscorrelation matrix at each rotation. Note that the rotation was nearly identical across modules. c , Rotation of each simultaneously recorded module between sessions (38 session pairs in 10 rats, as in ). Lines connect data from a single recording. A fourth module was recorded in 4 session pairs. Its rotation did not differ from the other simultaneously recorded modules . d , Difference in rotation between simultaneously recorded module pairs (n = 104 module pairs, each pair indicated by a circle). Red crosses indicate medians. Dashed gray line at 90° represents chance. e , Gray lines show coherent rotation between sessions for grid, head direction (HD), and border cells (n = 22 experiments). Lines connect data from a single recording.
Edf Trace V 1.0 Software, supplied by Marburg 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/edf trace v 1.0 software/product/Marburg GmbH
Average 90 stars, based on 1 article reviews
edf trace v 1.0 software - by Bioz Stars, 2026-06
90/100 stars
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Image Search Results


(A) Diagram of monosynaptic retrograde tracing assay using EnvA-coated G-deleted rabies virus expressing mCherry (EnvA-SADΔG-mcherry). G and TVA proteins were expressed in specific INs by the use of Cre mice together with AAV1-FLEX-TVA-2A-EGFP-2A-RVG (for Chx10+ and Vglut3+ INs) or lox-stop-lox-histone GFP-2A-TVA-2A-RVG mice (for Ptf1a+ INs). (B–D) Representative images of CSNs traced from Chx10+ (B), Ptf1a+ (C), and Vglut3+ (D) INs. In the panels, two images were combined to cover medial and laterals region of the cortex. White dotted lines show the cerebral cortex margins. Coronal section: right, medial; left, lateral. Scale bar, 100 μm. (E) Plotting of EnvA-SADΔG-mCherry+ CSNs traced from Chx10+ (red), Ptf1a+ (green), and Vglut3+ (blue) INs. Top view of the cortex. (F) Ratios of EnvA-SADΔG-mCherry+ CSNs traced from Chx10+ (red), Ptf1a+ (green), and Vglut3+ (blue) INs in ML % 1.7 mm, 1.7–2.0 mm, and R2.0 mm to total labeled neurons. Data are represented as mean ± SEM (n = 3). See also Figure S4.

Journal: Cell reports

Article Title: Corticospinal Circuits from the Sensory and Motor Cortices Differentially Regulate Skilled Movements through Distinct Spinal Interneurons

doi: 10.1016/j.celrep.2018.03.137

Figure Lengend Snippet: (A) Diagram of monosynaptic retrograde tracing assay using EnvA-coated G-deleted rabies virus expressing mCherry (EnvA-SADΔG-mcherry). G and TVA proteins were expressed in specific INs by the use of Cre mice together with AAV1-FLEX-TVA-2A-EGFP-2A-RVG (for Chx10+ and Vglut3+ INs) or lox-stop-lox-histone GFP-2A-TVA-2A-RVG mice (for Ptf1a+ INs). (B–D) Representative images of CSNs traced from Chx10+ (B), Ptf1a+ (C), and Vglut3+ (D) INs. In the panels, two images were combined to cover medial and laterals region of the cortex. White dotted lines show the cerebral cortex margins. Coronal section: right, medial; left, lateral. Scale bar, 100 μm. (E) Plotting of EnvA-SADΔG-mCherry+ CSNs traced from Chx10+ (red), Ptf1a+ (green), and Vglut3+ (blue) INs. Top view of the cortex. (F) Ratios of EnvA-SADΔG-mCherry+ CSNs traced from Chx10+ (red), Ptf1a+ (green), and Vglut3+ (blue) INs in ML % 1.7 mm, 1.7–2.0 mm, and R2.0 mm to total labeled neurons. Data are represented as mean ± SEM (n = 3). See also Figure S4.

Article Snippet: ​ REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Sheep polyclonal anti-GFP AbD Serotec 4745–1051; RRID:AB_619712 Rabbit polyclonal anti-GFP Invitrogen {"type":"entrez-nucleotide","attrs":{"text":"A11122","term_id":"490966","term_text":"A11122"}} A11122 ; RRID: AB_221569 Rat monoclonal anti-GFP Nacalai 04404–84; RRID: AB_10013361 Rabbit polyclonal anti-RFP Rockland 600–401-379; RRID: AB_2209751 Rabbit polyclonal anti-DsRed Clontech 632496; RRID: AB_10013483 Rabbit polyclonal anti-PKCγ Santa cruz sc-211; RRID: AB_632234 Rat monoclonal anti-Ctip2 Abcam ab18465; RRID: AB_10015215 Mouse monoclonal anti-NeuN Millipore MAB377; RRID: AB_2298772 Guinea pig polyclonal anti-Vglut1 Millipore AB5905; RRID: AB_2301751 Bacterial and Virus Strains PRV152 L. Enquist (Princeton Univ) N/A PRV614 L. Enquist (Princeton Univ) N/A AAV1-Syn-EGFP-Cre Penn vector core AV-1-PV1848 AAV1-CAG-tdTomato Penn vector core AV-1-PV3365 EnvA-SADΔG-mcherry E. Callaway and Gene Transfer, Targeting and Therapeutics Core (Salk Inst; Osakada et al., 2011 ) Addgene #32636 AAV1-Syn-FLEX-TVA-2A-EGFP-2A-RVG UNC vector core Addgene #52473 AAV1-CAG-ChR2(H134R)-mCherry Penn vector core AV-1–20938M AAV8-hSyn-DIO-hM4D(Gi)-mCherry UNC vector core Addgene #44362 Chemicals, Peptides, and Recombinant Proteins Green Retrobeads IX Lumafluor N/A Biotinylated dextran amine (10,000MW) Invitrogen D-1956 Fluorogold Fluorochrome N/A Clozapine-N-oxide Sigma-Aldrich C0832–5MG Experimental Models: Organisms/Strains Mouse: Rbp4-Cre GENSAT, MMRRC MMRRC:031125-UCD; MGI:4367067 Mouse: En1-Cre A. Joyner (Memorial Sloan Kettering Cancer Center; Kimmel et al., 2000 ) MGI:2446434 Mouse: Chx10-Cre Azim et al., 2014 N/A Mouse: Chat-Cre The Jackson Laboratory JAX# 006410; MGI: 5475195 Mouse: Ptf1a-Cre C. Wright(Vanderbilt Univ.

Techniques: Retrograde Tracing, Expressing, Labeling

Highlights

Journal: Cell reports

Article Title: Corticospinal Circuits from the Sensory and Motor Cortices Differentially Regulate Skilled Movements through Distinct Spinal Interneurons

doi: 10.1016/j.celrep.2018.03.137

Figure Lengend Snippet: Highlights

Article Snippet: ​ REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies Sheep polyclonal anti-GFP AbD Serotec 4745–1051; RRID:AB_619712 Rabbit polyclonal anti-GFP Invitrogen {"type":"entrez-nucleotide","attrs":{"text":"A11122","term_id":"490966","term_text":"A11122"}} A11122 ; RRID: AB_221569 Rat monoclonal anti-GFP Nacalai 04404–84; RRID: AB_10013361 Rabbit polyclonal anti-RFP Rockland 600–401-379; RRID: AB_2209751 Rabbit polyclonal anti-DsRed Clontech 632496; RRID: AB_10013483 Rabbit polyclonal anti-PKCγ Santa cruz sc-211; RRID: AB_632234 Rat monoclonal anti-Ctip2 Abcam ab18465; RRID: AB_10015215 Mouse monoclonal anti-NeuN Millipore MAB377; RRID: AB_2298772 Guinea pig polyclonal anti-Vglut1 Millipore AB5905; RRID: AB_2301751 Bacterial and Virus Strains PRV152 L. Enquist (Princeton Univ) N/A PRV614 L. Enquist (Princeton Univ) N/A AAV1-Syn-EGFP-Cre Penn vector core AV-1-PV1848 AAV1-CAG-tdTomato Penn vector core AV-1-PV3365 EnvA-SADΔG-mcherry E. Callaway and Gene Transfer, Targeting and Therapeutics Core (Salk Inst; Osakada et al., 2011 ) Addgene #32636 AAV1-Syn-FLEX-TVA-2A-EGFP-2A-RVG UNC vector core Addgene #52473 AAV1-CAG-ChR2(H134R)-mCherry Penn vector core AV-1–20938M AAV8-hSyn-DIO-hM4D(Gi)-mCherry UNC vector core Addgene #44362 Chemicals, Peptides, and Recombinant Proteins Green Retrobeads IX Lumafluor N/A Biotinylated dextran amine (10,000MW) Invitrogen D-1956 Fluorogold Fluorochrome N/A Clozapine-N-oxide Sigma-Aldrich C0832–5MG Experimental Models: Organisms/Strains Mouse: Rbp4-Cre GENSAT, MMRRC MMRRC:031125-UCD; MGI:4367067 Mouse: En1-Cre A. Joyner (Memorial Sloan Kettering Cancer Center; Kimmel et al., 2000 ) MGI:2446434 Mouse: Chx10-Cre Azim et al., 2014 N/A Mouse: Chat-Cre The Jackson Laboratory JAX# 006410; MGI: 5475195 Mouse: Ptf1a-Cre C. Wright(Vanderbilt Univ.

Techniques: Plasmid Preparation, Recombinant, Software

a , Module crosscorrelograms for sessions in different rooms (A1×B1) at incremental degrees of rotation in rat #26718 (select number of rotations shown here for visualization purposes; see for additional rotations) (as in , right). Asterisks denote overall maximum for each module. b , Maximum correlation between 3D stacks of rate maps of sessions A1 and B1 (with cell identity along the z-axis) as a function of rotation for each module in rat #26718. Maximum correlation refers to the highest value within the crosscorrelation matrix at each rotation. Note that the rotation was nearly identical across modules. c , Rotation of each simultaneously recorded module between sessions (38 session pairs in 10 rats, as in ). Lines connect data from a single recording. A fourth module was recorded in 4 session pairs. Its rotation did not differ from the other simultaneously recorded modules . d , Difference in rotation between simultaneously recorded module pairs (n = 104 module pairs, each pair indicated by a circle). Red crosses indicate medians. Dashed gray line at 90° represents chance. e , Gray lines show coherent rotation between sessions for grid, head direction (HD), and border cells (n = 22 experiments). Lines connect data from a single recording.

Journal: bioRxiv

Article Title: Functional independence of entorhinal grid cell modules enables remapping in hippocampal place cells

doi: 10.1101/2025.09.24.677985

Figure Lengend Snippet: a , Module crosscorrelograms for sessions in different rooms (A1×B1) at incremental degrees of rotation in rat #26718 (select number of rotations shown here for visualization purposes; see for additional rotations) (as in , right). Asterisks denote overall maximum for each module. b , Maximum correlation between 3D stacks of rate maps of sessions A1 and B1 (with cell identity along the z-axis) as a function of rotation for each module in rat #26718. Maximum correlation refers to the highest value within the crosscorrelation matrix at each rotation. Note that the rotation was nearly identical across modules. c , Rotation of each simultaneously recorded module between sessions (38 session pairs in 10 rats, as in ). Lines connect data from a single recording. A fourth module was recorded in 4 session pairs. Its rotation did not differ from the other simultaneously recorded modules . d , Difference in rotation between simultaneously recorded module pairs (n = 104 module pairs, each pair indicated by a circle). Red crosses indicate medians. Dashed gray line at 90° represents chance. e , Gray lines show coherent rotation between sessions for grid, head direction (HD), and border cells (n = 22 experiments). Lines connect data from a single recording.

Article Snippet: These markers were tracked at 120 Hz with a 3D motion capture system (six overhead OptiTrack Flex 13 cameras and Motive recording software).

Techniques: