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aavrg ef1a mcherry ires cre  (Addgene inc)


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    Structured Review

    Addgene inc aavrg ef1a mcherry ires cre
    Aavrg Ef1a Mcherry Ires Cre, supplied by Addgene inc, used in various techniques. Bioz Stars score: 96/100, based on 311 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/penn+aav+hsyn+cre+wpre+hgh/pENN%2EAAV%2EhSyn%2ECre%2EWPRE%2EhGH+(Plasmid+%23105553)/pmc13621956-927-0-9
    Average 96 stars, based on 311 article reviews
    aavrg ef1a mcherry ires cre - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Labeling:

    Article Title: A High-Resolution Transcriptomic Atlas of Cell Types in the Ventral Visual Thalamus.
    Article Snippet: .. Monosynaptic labeling of retinorecipient neurons in the vLGN was achieved using bilateral intravitreal injections of pENN.AAV.hSyn.Cre.WPRE.hGH (2.5 × 1013 GC/mL; Addgene viral prep #105553- AAV1; RRID:Addgene_105 553; referred to here as AAV1- Cre). ..

    Injection:

    Article Title: Alarm pheromone activates posterior medial amygdala-to-bed nucleus of the stria terminalis projections in male rats.
    Article Snippet: .. Then, the rats assigned to the hSyn group (n = 9) received a unilateral injection of 0.2 μL of a 1:1 mixture of pAAVCBA-FLEX-SYP-mCherry (produced and packaged in one of our authors’ lab; Uematsu et al., 2017) and pENN-AAV-hSyn-Cre-WPRE-hGH (gifted from Dr. James M. Wilson; Addgene viral prep # 105553-AAV1, htt ps://n2t.net/addgene:105553, RRID: Addgene_105553) directed at the left pvMeA (AP, 3.00; ML, − 1.00; DV, 6.50 mm; Paxinos and Watson, 2007). .. Similarly, a unilateral injection of 0.2 μL of a 1:1 mixture of pAAV-CBA-FLEX-SYP-mCherry (gifted from Dr. Akira Uematsu) and pENN-AAV-CaMKII 0.4-Cre-SV40 (gifted from Dr. James M. Wilson; Addgene viral prep # 105558-AAV1; https://n2t.net/addgene:105558, RRID: Addgene_105558) was directed at the left pvMeA in the rats assigned to the CaMKII group (n = 9).

    Article Title: Co-Conservation of synaptic gene expression and circuitry in collicular neurons
    Article Snippet: .. Four weeks after pENN.AAV.hSyn.Cre.WPRE.hGH (Addgene, Catalog # 105553-AAVrg) was injected into the pulvinar of H2B-TRAP mice, their brains were harvested following rapid decapitation to minimize the effects of stress on gene expression. ..

    Article Title: Targeting the noradrenergic-metabolic axis: A new strategy for sugar-induced depression subtypes.
    Article Snippet: .. We injected 500 nl of pAAV-hSyn-DIO-hM3D(Gq)-mCherry (AAV retrograde; gifted by Bryan Roth, Addgene viral prep # 44361-AAV Retrograde; RRID: Addgene_44361; titre: 0.625 1013 viral genomes ml 1) into both sides of the PFC (AP: +1.7 mm, ML: ±0.3 mm, DV: 2.3 mm) and 300 nl of pENN-AAV-hSyn-Cre-WPRE-hGH (AAV9; gifted by James M. Wilson, Addgene viral prep # 105553-AAV9; RRID: Addgene_ 105553; titre: 1.15 1013 viral genomes ml 1) into both sides of the LC (AP: 5.4 mm, ML: ±0.8 mm, DV: 3.5 mm). ..

    Article Title: Co-Conservation of synaptic gene expression and circuitry in collicular neurons.
    Article Snippet: .. This identified a total of 982 cluster marker genes that were detected in more than 10% of neurons inside the selected cluster and the minimal outside. snRNA-seq of pulvinar-projecting neurons in mouse SC Four weeks after pENN.AAV.hSyn.Cre.WPRE.hGH (Addgene, Catalog # 105553-AAVrg) was injected into the pulvinar of H2B-TRAP mice, their brains were harvested following rapid decapitation to minimize the effects of stress on gene expression. ..

    Produced:

    Article Title: Alarm pheromone activates posterior medial amygdala-to-bed nucleus of the stria terminalis projections in male rats.
    Article Snippet: .. Then, the rats assigned to the hSyn group (n = 9) received a unilateral injection of 0.2 μL of a 1:1 mixture of pAAVCBA-FLEX-SYP-mCherry (produced and packaged in one of our authors’ lab; Uematsu et al., 2017) and pENN-AAV-hSyn-Cre-WPRE-hGH (gifted from Dr. James M. Wilson; Addgene viral prep # 105553-AAV1, htt ps://n2t.net/addgene:105553, RRID: Addgene_105553) directed at the left pvMeA (AP, 3.00; ML, − 1.00; DV, 6.50 mm; Paxinos and Watson, 2007). .. Similarly, a unilateral injection of 0.2 μL of a 1:1 mixture of pAAV-CBA-FLEX-SYP-mCherry (gifted from Dr. Akira Uematsu) and pENN-AAV-CaMKII 0.4-Cre-SV40 (gifted from Dr. James M. Wilson; Addgene viral prep # 105558-AAV1; https://n2t.net/addgene:105558, RRID: Addgene_105558) was directed at the left pvMeA in the rats assigned to the CaMKII group (n = 9).

    Bioprocessing:

    Article Title: Targeting the noradrenergic-metabolic axis: A new strategy for sugar-induced depression subtypes.
    Article Snippet: .. We thank Addgene for providing the viral vectors pAAV-hSyn-DIO-hM3D (Gq)-mCherry (AAV Retrograde; Addgene viral prep #44361-AAV Ret- rograde; RRID: Addgene_44361) originally deposited by Bryan Roth, and pENN-AAV-hSyn-Cre-WPRE-hGH (AAV9; Addgene viral prep #105553-AAV9; RRID: Addgene_105553) originally deposited by James M. Wilson. ..

    Article Title: Targeting the noradrenergic-metabolic axis: A new strategy for sugar-induced depression subtypes.
    Article Snippet: .. We injected 500 nl of pAAV-hSyn-DIO-hM3D(Gq)-mCherry (AAV retrograde; gifted by Bryan Roth, Addgene viral prep # 44361-AAV Retrograde; RRID: Addgene_44361; titre: 0.625 1013 viral genomes ml 1) into both sides of the PFC (AP: +1.7 mm, ML: ±0.3 mm, DV: 2.3 mm) and 300 nl of pENN-AAV-hSyn-Cre-WPRE-hGH (AAV9; gifted by James M. Wilson, Addgene viral prep # 105553-AAV9; RRID: Addgene_ 105553; titre: 1.15 1013 viral genomes ml 1) into both sides of the LC (AP: 5.4 mm, ML: ±0.8 mm, DV: 3.5 mm). ..

    Gene Expression:

    Article Title: Co-Conservation of synaptic gene expression and circuitry in collicular neurons
    Article Snippet: .. Four weeks after pENN.AAV.hSyn.Cre.WPRE.hGH (Addgene, Catalog # 105553-AAVrg) was injected into the pulvinar of H2B-TRAP mice, their brains were harvested following rapid decapitation to minimize the effects of stress on gene expression. ..

    Article Title: Co-Conservation of synaptic gene expression and circuitry in collicular neurons.
    Article Snippet: .. This identified a total of 982 cluster marker genes that were detected in more than 10% of neurons inside the selected cluster and the minimal outside. snRNA-seq of pulvinar-projecting neurons in mouse SC Four weeks after pENN.AAV.hSyn.Cre.WPRE.hGH (Addgene, Catalog # 105553-AAVrg) was injected into the pulvinar of H2B-TRAP mice, their brains were harvested following rapid decapitation to minimize the effects of stress on gene expression. ..

    Marker:

    Article Title: Co-Conservation of synaptic gene expression and circuitry in collicular neurons.
    Article Snippet: .. This identified a total of 982 cluster marker genes that were detected in more than 10% of neurons inside the selected cluster and the minimal outside. snRNA-seq of pulvinar-projecting neurons in mouse SC Four weeks after pENN.AAV.hSyn.Cre.WPRE.hGH (Addgene, Catalog # 105553-AAVrg) was injected into the pulvinar of H2B-TRAP mice, their brains were harvested following rapid decapitation to minimize the effects of stress on gene expression. ..

    other:

    Article Title: Co-Conservation of synaptic gene expression and circuitry in collicular neurons.
    Article Snippet: cDNA libraries were then sequenced on an Illumina NextSeq 2000 platform to an average depth of 28,135 reads per cell.



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    (A) Schematic of retrograde labeling of input projection neurons to the VTA using <t>AAV.rg-hSyn1-EGFP.</t> (B) Micrograph of an exemplary coronal brain section upon machine learning-assisted brain region mapping (Aligning Big Brains & Atlases (ABBA/ImageJ)). Back-labeled neurons are highlighted in the mPFC and LHA. (C) Circos plot showing relative input strength from reward-related regions to the VTA comparing eBED-prone versus-resilient Tet1 +/– mice (upper panel); corresponding binge sizes of individual Tet1 +/- mice across 5 eBED days plotted on a Log 10 scale to visualize varied responses (lower panel; shaded area shows normal binge response). Data are presented as mean minimum to maximum values. ** P < 0.01. n = 4 mice (unpaired Student’s t -test). (D) Coronal brain schematics of mPFC subregions ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). (E) Representative micrographs of mPFC PL from eBED-prone versus-resilient Tet1 +/− mice. Scale bar 100 μm. (F) Bar graphs of raw EGFP density values from mPFC subregions hemisections ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). Data are presented as mean ± SEM. * P < 0.05. n = 4 mice (two-tailed unpaired Student’s t -test). (G) Schematic illustrating chemogenetic approach to selectively inhibit VTA-projecting mPFC PL neurons using a dual AAV approach (AAV.rg-Cre + AAV-hSyn1-FLEX-hM4Di-mCherry). (H) Micrograph of VTA-projecting mPFC PL neurons expressing mCherry (red) intermingled with layer-5 pyramidal neurons (CTIP2: grey). Scale bar: 500 μm and 50 μm (insert). (I) Cumulative binge intake of hM4Di mPFC-VTA mice and controls per individual days (left panel). Data are presented as mean ± SEM. *** P < 0.001, **** P < 0.0001. n = 4–5 mice (multiple unpaired Student’s t -test); mean binge sizes of hM4Di mPFC-VTA mice and controls (right panel). Data are presented as mean and minimum to maximum. * P < 0.05, n = 4–5 mice (one-tailed unpaired Student’s t -test).
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    (A) Schematic of retrograde labeling of input projection neurons to the VTA using <t>AAV.rg-hSyn1-EGFP.</t> (B) Micrograph of an exemplary coronal brain section upon machine learning-assisted brain region mapping (Aligning Big Brains & Atlases (ABBA/ImageJ)). Back-labeled neurons are highlighted in the mPFC and LHA. (C) Circos plot showing relative input strength from reward-related regions to the VTA comparing eBED-prone versus-resilient Tet1 +/– mice (upper panel); corresponding binge sizes of individual Tet1 +/- mice across 5 eBED days plotted on a Log 10 scale to visualize varied responses (lower panel; shaded area shows normal binge response). Data are presented as mean minimum to maximum values. ** P < 0.01. n = 4 mice (unpaired Student’s t -test). (D) Coronal brain schematics of mPFC subregions ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). (E) Representative micrographs of mPFC PL from eBED-prone versus-resilient Tet1 +/− mice. Scale bar 100 μm. (F) Bar graphs of raw EGFP density values from mPFC subregions hemisections ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). Data are presented as mean ± SEM. * P < 0.05. n = 4 mice (two-tailed unpaired Student’s t -test). (G) Schematic illustrating chemogenetic approach to selectively inhibit VTA-projecting mPFC PL neurons using a dual AAV approach (AAV.rg-Cre + AAV-hSyn1-FLEX-hM4Di-mCherry). (H) Micrograph of VTA-projecting mPFC PL neurons expressing mCherry (red) intermingled with layer-5 pyramidal neurons (CTIP2: grey). Scale bar: 500 μm and 50 μm (insert). (I) Cumulative binge intake of hM4Di mPFC-VTA mice and controls per individual days (left panel). Data are presented as mean ± SEM. *** P < 0.001, **** P < 0.0001. n = 4–5 mice (multiple unpaired Student’s t -test); mean binge sizes of hM4Di mPFC-VTA mice and controls (right panel). Data are presented as mean and minimum to maximum. * P < 0.05, n = 4–5 mice (one-tailed unpaired Student’s t -test).
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    (A) Schematic of retrograde labeling of input projection neurons to the VTA using <t>AAV.rg-hSyn1-EGFP.</t> (B) Micrograph of an exemplary coronal brain section upon machine learning-assisted brain region mapping (Aligning Big Brains & Atlases (ABBA/ImageJ)). Back-labeled neurons are highlighted in the mPFC and LHA. (C) Circos plot showing relative input strength from reward-related regions to the VTA comparing eBED-prone versus-resilient Tet1 +/– mice (upper panel); corresponding binge sizes of individual Tet1 +/- mice across 5 eBED days plotted on a Log 10 scale to visualize varied responses (lower panel; shaded area shows normal binge response). Data are presented as mean minimum to maximum values. ** P < 0.01. n = 4 mice (unpaired Student’s t -test). (D) Coronal brain schematics of mPFC subregions ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). (E) Representative micrographs of mPFC PL from eBED-prone versus-resilient Tet1 +/− mice. Scale bar 100 μm. (F) Bar graphs of raw EGFP density values from mPFC subregions hemisections ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). Data are presented as mean ± SEM. * P < 0.05. n = 4 mice (two-tailed unpaired Student’s t -test). (G) Schematic illustrating chemogenetic approach to selectively inhibit VTA-projecting mPFC PL neurons using a dual AAV approach (AAV.rg-Cre + AAV-hSyn1-FLEX-hM4Di-mCherry). (H) Micrograph of VTA-projecting mPFC PL neurons expressing mCherry (red) intermingled with layer-5 pyramidal neurons (CTIP2: grey). Scale bar: 500 μm and 50 μm (insert). (I) Cumulative binge intake of hM4Di mPFC-VTA mice and controls per individual days (left panel). Data are presented as mean ± SEM. *** P < 0.001, **** P < 0.0001. n = 4–5 mice (multiple unpaired Student’s t -test); mean binge sizes of hM4Di mPFC-VTA mice and controls (right panel). Data are presented as mean and minimum to maximum. * P < 0.05, n = 4–5 mice (one-tailed unpaired Student’s t -test).
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    (A) Schematic of retrograde labeling of input projection neurons to the VTA using <t>AAV.rg-hSyn1-EGFP.</t> (B) Micrograph of an exemplary coronal brain section upon machine learning-assisted brain region mapping (Aligning Big Brains & Atlases (ABBA/ImageJ)). Back-labeled neurons are highlighted in the mPFC and LHA. (C) Circos plot showing relative input strength from reward-related regions to the VTA comparing eBED-prone versus-resilient Tet1 +/– mice (upper panel); corresponding binge sizes of individual Tet1 +/- mice across 5 eBED days plotted on a Log 10 scale to visualize varied responses (lower panel; shaded area shows normal binge response). Data are presented as mean minimum to maximum values. ** P < 0.01. n = 4 mice (unpaired Student’s t -test). (D) Coronal brain schematics of mPFC subregions ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). (E) Representative micrographs of mPFC PL from eBED-prone versus-resilient Tet1 +/− mice. Scale bar 100 μm. (F) Bar graphs of raw EGFP density values from mPFC subregions hemisections ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). Data are presented as mean ± SEM. * P < 0.05. n = 4 mice (two-tailed unpaired Student’s t -test). (G) Schematic illustrating chemogenetic approach to selectively inhibit VTA-projecting mPFC PL neurons using a dual AAV approach (AAV.rg-Cre + AAV-hSyn1-FLEX-hM4Di-mCherry). (H) Micrograph of VTA-projecting mPFC PL neurons expressing mCherry (red) intermingled with layer-5 pyramidal neurons (CTIP2: grey). Scale bar: 500 μm and 50 μm (insert). (I) Cumulative binge intake of hM4Di mPFC-VTA mice and controls per individual days (left panel). Data are presented as mean ± SEM. *** P < 0.001, **** P < 0.0001. n = 4–5 mice (multiple unpaired Student’s t -test); mean binge sizes of hM4Di mPFC-VTA mice and controls (right panel). Data are presented as mean and minimum to maximum. * P < 0.05, n = 4–5 mice (one-tailed unpaired Student’s t -test).
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    (A) Schematic of retrograde labeling of input projection neurons to the VTA using <t>AAV.rg-hSyn1-EGFP.</t> (B) Micrograph of an exemplary coronal brain section upon machine learning-assisted brain region mapping (Aligning Big Brains & Atlases (ABBA/ImageJ)). Back-labeled neurons are highlighted in the mPFC and LHA. (C) Circos plot showing relative input strength from reward-related regions to the VTA comparing eBED-prone versus-resilient Tet1 +/– mice (upper panel); corresponding binge sizes of individual Tet1 +/- mice across 5 eBED days plotted on a Log 10 scale to visualize varied responses (lower panel; shaded area shows normal binge response). Data are presented as mean minimum to maximum values. ** P < 0.01. n = 4 mice (unpaired Student’s t -test). (D) Coronal brain schematics of mPFC subregions ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). (E) Representative micrographs of mPFC PL from eBED-prone versus-resilient Tet1 +/− mice. Scale bar 100 μm. (F) Bar graphs of raw EGFP density values from mPFC subregions hemisections ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). Data are presented as mean ± SEM. * P < 0.05. n = 4 mice (two-tailed unpaired Student’s t -test). (G) Schematic illustrating chemogenetic approach to selectively inhibit VTA-projecting mPFC PL neurons using a dual AAV approach (AAV.rg-Cre + AAV-hSyn1-FLEX-hM4Di-mCherry). (H) Micrograph of VTA-projecting mPFC PL neurons expressing mCherry (red) intermingled with layer-5 pyramidal neurons (CTIP2: grey). Scale bar: 500 μm and 50 μm (insert). (I) Cumulative binge intake of hM4Di mPFC-VTA mice and controls per individual days (left panel). Data are presented as mean ± SEM. *** P < 0.001, **** P < 0.0001. n = 4–5 mice (multiple unpaired Student’s t -test); mean binge sizes of hM4Di mPFC-VTA mice and controls (right panel). Data are presented as mean and minimum to maximum. * P < 0.05, n = 4–5 mice (one-tailed unpaired Student’s t -test).
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    Image Search Results


    (A) Schematic of retrograde labeling of input projection neurons to the VTA using AAV.rg-hSyn1-EGFP. (B) Micrograph of an exemplary coronal brain section upon machine learning-assisted brain region mapping (Aligning Big Brains & Atlases (ABBA/ImageJ)). Back-labeled neurons are highlighted in the mPFC and LHA. (C) Circos plot showing relative input strength from reward-related regions to the VTA comparing eBED-prone versus-resilient Tet1 +/– mice (upper panel); corresponding binge sizes of individual Tet1 +/- mice across 5 eBED days plotted on a Log 10 scale to visualize varied responses (lower panel; shaded area shows normal binge response). Data are presented as mean minimum to maximum values. ** P < 0.01. n = 4 mice (unpaired Student’s t -test). (D) Coronal brain schematics of mPFC subregions ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). (E) Representative micrographs of mPFC PL from eBED-prone versus-resilient Tet1 +/− mice. Scale bar 100 μm. (F) Bar graphs of raw EGFP density values from mPFC subregions hemisections ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). Data are presented as mean ± SEM. * P < 0.05. n = 4 mice (two-tailed unpaired Student’s t -test). (G) Schematic illustrating chemogenetic approach to selectively inhibit VTA-projecting mPFC PL neurons using a dual AAV approach (AAV.rg-Cre + AAV-hSyn1-FLEX-hM4Di-mCherry). (H) Micrograph of VTA-projecting mPFC PL neurons expressing mCherry (red) intermingled with layer-5 pyramidal neurons (CTIP2: grey). Scale bar: 500 μm and 50 μm (insert). (I) Cumulative binge intake of hM4Di mPFC-VTA mice and controls per individual days (left panel). Data are presented as mean ± SEM. *** P < 0.001, **** P < 0.0001. n = 4–5 mice (multiple unpaired Student’s t -test); mean binge sizes of hM4Di mPFC-VTA mice and controls (right panel). Data are presented as mean and minimum to maximum. * P < 0.05, n = 4–5 mice (one-tailed unpaired Student’s t -test).

    Journal: bioRxiv

    Article Title: Midbrain Tet1 dosage defines inter-individual binge-eating susceptibility

    doi: 10.64898/2026.03.14.711800

    Figure Lengend Snippet: (A) Schematic of retrograde labeling of input projection neurons to the VTA using AAV.rg-hSyn1-EGFP. (B) Micrograph of an exemplary coronal brain section upon machine learning-assisted brain region mapping (Aligning Big Brains & Atlases (ABBA/ImageJ)). Back-labeled neurons are highlighted in the mPFC and LHA. (C) Circos plot showing relative input strength from reward-related regions to the VTA comparing eBED-prone versus-resilient Tet1 +/– mice (upper panel); corresponding binge sizes of individual Tet1 +/- mice across 5 eBED days plotted on a Log 10 scale to visualize varied responses (lower panel; shaded area shows normal binge response). Data are presented as mean minimum to maximum values. ** P < 0.01. n = 4 mice (unpaired Student’s t -test). (D) Coronal brain schematics of mPFC subregions ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). (E) Representative micrographs of mPFC PL from eBED-prone versus-resilient Tet1 +/− mice. Scale bar 100 μm. (F) Bar graphs of raw EGFP density values from mPFC subregions hemisections ( PL : prelimbic; Cg1 : dorsal cingulate cortex; Cg2 : ventral cingulate cortex). Data are presented as mean ± SEM. * P < 0.05. n = 4 mice (two-tailed unpaired Student’s t -test). (G) Schematic illustrating chemogenetic approach to selectively inhibit VTA-projecting mPFC PL neurons using a dual AAV approach (AAV.rg-Cre + AAV-hSyn1-FLEX-hM4Di-mCherry). (H) Micrograph of VTA-projecting mPFC PL neurons expressing mCherry (red) intermingled with layer-5 pyramidal neurons (CTIP2: grey). Scale bar: 500 μm and 50 μm (insert). (I) Cumulative binge intake of hM4Di mPFC-VTA mice and controls per individual days (left panel). Data are presented as mean ± SEM. *** P < 0.001, **** P < 0.0001. n = 4–5 mice (multiple unpaired Student’s t -test); mean binge sizes of hM4Di mPFC-VTA mice and controls (right panel). Data are presented as mean and minimum to maximum. * P < 0.05, n = 4–5 mice (one-tailed unpaired Student’s t -test).

    Article Snippet: To perform brain-wide mapping of VTA inputs, AAV rg -hSyn1-EGFP (Addgene, #105553, 7E12 GC/mL) was bilaterally injected into the VTA of 6–8-week-old Tet1 +/– mice and littermate controls.

    Techniques: Labeling, Two Tailed Test, Expressing, One-tailed Test