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dsred max n1  (Addgene inc)


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    Structured Review

    Addgene inc dsred max n1
    A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D) or empty <t>vector</t> <t>and</t> <t>DsRed-Max-N1</t> plasmids, and fixed at DIV6 for confocal fluorescence microscopy analysis. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-positive neurons or control neurons (empty vector) is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 double DsRed-/YFP-ArfGAP1-positive neurons, or single DsRed-positive neurons (control), across at least three independent experiments/cultures. *** P <0.001 or **** P <0.0001 compared to control (DsRed alone), or as indicated, by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.
    Dsred Max N1, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/dsred max n1/product/Addgene inc
    Average 93 stars, based on 17 article reviews
    dsred max n1 - by Bioz Stars, 2026-05
    93/100 stars

    Images

    1) Product Images from "LRRK2 regulates ArfGAP1 membrane localization, activity and neuronal toxicity via phosphorylation within its lipid-sensing ALPS2 motif"

    Article Title: LRRK2 regulates ArfGAP1 membrane localization, activity and neuronal toxicity via phosphorylation within its lipid-sensing ALPS2 motif

    Journal: bioRxiv

    doi: 10.64898/2026.01.12.699049

    A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D) or empty vector and DsRed-Max-N1 plasmids, and fixed at DIV6 for confocal fluorescence microscopy analysis. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-positive neurons or control neurons (empty vector) is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 double DsRed-/YFP-ArfGAP1-positive neurons, or single DsRed-positive neurons (control), across at least three independent experiments/cultures. *** P <0.001 or **** P <0.0001 compared to control (DsRed alone), or as indicated, by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.
    Figure Legend Snippet: A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D) or empty vector and DsRed-Max-N1 plasmids, and fixed at DIV6 for confocal fluorescence microscopy analysis. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-positive neurons or control neurons (empty vector) is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 double DsRed-/YFP-ArfGAP1-positive neurons, or single DsRed-positive neurons (control), across at least three independent experiments/cultures. *** P <0.001 or **** P <0.0001 compared to control (DsRed alone), or as indicated, by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.

    Techniques Used: Transfection, Plasmid Preparation, Fluorescence, Microscopy, Labeling, Control

    A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D), FLAG-LRRK2 (G2019S) and DsRed-Max-N1 plasmids, and fixed at DIV6 for immunofluorescence analysis with anti-FLAG antibody. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green), G2019S LRRK2 (yellow) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-/LRRK2-positive neurons is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 triple DsRed-/YFP-ArfGAP1-/LRRK2-positive neurons across at least three independent experiments/cultures. **** P <0.0001 compared to WT ArfGAP1/LRRK2 by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.
    Figure Legend Snippet: A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D), FLAG-LRRK2 (G2019S) and DsRed-Max-N1 plasmids, and fixed at DIV6 for immunofluorescence analysis with anti-FLAG antibody. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green), G2019S LRRK2 (yellow) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-/LRRK2-positive neurons is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 triple DsRed-/YFP-ArfGAP1-/LRRK2-positive neurons across at least three independent experiments/cultures. **** P <0.0001 compared to WT ArfGAP1/LRRK2 by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.

    Techniques Used: Transfection, Immunofluorescence, Labeling



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    A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D) or empty <t>vector</t> <t>and</t> <t>DsRed-Max-N1</t> plasmids, and fixed at DIV6 for confocal fluorescence microscopy analysis. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-positive neurons or control neurons (empty vector) is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 double DsRed-/YFP-ArfGAP1-positive neurons, or single DsRed-positive neurons (control), across at least three independent experiments/cultures. *** P <0.001 or **** P <0.0001 compared to control (DsRed alone), or as indicated, by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.
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    Fluorescence microscope images showing exogenous <t>dsRed</t> expression following transfection of <t>MAu/DNA/siRNA</t> LbL nanoparticles. Lipofectamine® 2000 was added at a 100 ng dosage 2.5 μL:1 μg dsRed DNA; (200 ms eGFP and 600 ms dsRed exposure time; magnification of 10x).
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    Fluorescence microscope images showing exogenous <t>dsRed</t> expression following transfection of <t>MAu/DNA/siRNA</t> LbL nanoparticles. Lipofectamine® 2000 was added at a 100 ng dosage 2.5 μL:1 μg dsRed DNA; (200 ms eGFP and 600 ms dsRed exposure time; magnification of 10x).
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    Image Search Results


    A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D) or empty vector and DsRed-Max-N1 plasmids, and fixed at DIV6 for confocal fluorescence microscopy analysis. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-positive neurons or control neurons (empty vector) is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 double DsRed-/YFP-ArfGAP1-positive neurons, or single DsRed-positive neurons (control), across at least three independent experiments/cultures. *** P <0.001 or **** P <0.0001 compared to control (DsRed alone), or as indicated, by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.

    Journal: bioRxiv

    Article Title: LRRK2 regulates ArfGAP1 membrane localization, activity and neuronal toxicity via phosphorylation within its lipid-sensing ALPS2 motif

    doi: 10.64898/2026.01.12.699049

    Figure Lengend Snippet: A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D) or empty vector and DsRed-Max-N1 plasmids, and fixed at DIV6 for confocal fluorescence microscopy analysis. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-positive neurons or control neurons (empty vector) is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 double DsRed-/YFP-ArfGAP1-positive neurons, or single DsRed-positive neurons (control), across at least three independent experiments/cultures. *** P <0.001 or **** P <0.0001 compared to control (DsRed alone), or as indicated, by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.

    Article Snippet: A plasmid containing DsRed-Max-N1 was obtained from Addgene (#21718) [ ].

    Techniques: Transfection, Plasmid Preparation, Fluorescence, Microscopy, Labeling, Control

    A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D), FLAG-LRRK2 (G2019S) and DsRed-Max-N1 plasmids, and fixed at DIV6 for immunofluorescence analysis with anti-FLAG antibody. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green), G2019S LRRK2 (yellow) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-/LRRK2-positive neurons is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 triple DsRed-/YFP-ArfGAP1-/LRRK2-positive neurons across at least three independent experiments/cultures. **** P <0.0001 compared to WT ArfGAP1/LRRK2 by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.

    Journal: bioRxiv

    Article Title: LRRK2 regulates ArfGAP1 membrane localization, activity and neuronal toxicity via phosphorylation within its lipid-sensing ALPS2 motif

    doi: 10.64898/2026.01.12.699049

    Figure Lengend Snippet: A ) Rat primary cortical neurons were co-transfected at DIV3 with YFP-ArfGAP1 (WT, 3A or 3D), FLAG-LRRK2 (G2019S) and DsRed-Max-N1 plasmids, and fixed at DIV6 for immunofluorescence analysis with anti-FLAG antibody. Fluorescent images reveal the co-labeling of cortical neurons with YFP-ArfGAP1 (green), G2019S LRRK2 (yellow) and DsRed (red), with the DsRed images pseudo colored (ICA) to enhance the contrast of neuritic processes. Neuronal soma (white arrows) and axonal processes (black arrowheads) are indicated. Scale bars: 50 μm. B ) Quantitative analysis of DsRed-positive axon length in YFP-ArfGAP1-/LRRK2-positive neurons is shown. Bars represent the mean ± SEM axon length (in μm) from 90-120 triple DsRed-/YFP-ArfGAP1-/LRRK2-positive neurons across at least three independent experiments/cultures. **** P <0.0001 compared to WT ArfGAP1/LRRK2 by one-way ANOVA with Dunnett’s multiple comparisons test. ns , non-significant.

    Article Snippet: A plasmid containing DsRed-Max-N1 was obtained from Addgene (#21718) [ ].

    Techniques: Transfection, Immunofluorescence, Labeling

    Journal: eLife

    Article Title: Auxiliary subunits keep AMPA receptors compact during activation and desensitization

    doi: 10.7554/eLife.40548

    Figure Lengend Snippet:

    Article Snippet: Transfected construct ( Mus musculus ) , Stargazin; Stg , Other , ID_GenBank: NM_007583.2 , Gift from Susumu Tomita; vector: pRK5 with IRES dsRed (dsRed_Max Addgene plasmid: 21718)..

    Techniques: Transfection, Construct, Plasmid Preparation, Concentration Assay, Software

    Fluorescence microscope images showing exogenous dsRed expression following transfection of MAu/DNA/siRNA LbL nanoparticles. Lipofectamine® 2000 was added at a 100 ng dosage 2.5 μL:1 μg dsRed DNA; (200 ms eGFP and 600 ms dsRed exposure time; magnification of 10x).

    Journal: Acta biomaterialia

    Article Title: Degradable Polymer-Coated Gold Nanoparticles for Co-Delivery of DNA and siRNA

    doi: 10.1016/j.actbio.2014.09.020

    Figure Lengend Snippet: Fluorescence microscope images showing exogenous dsRed expression following transfection of MAu/DNA/siRNA LbL nanoparticles. Lipofectamine® 2000 was added at a 100 ng dosage 2.5 μL:1 μg dsRed DNA; (200 ms eGFP and 600 ms dsRed exposure time; magnification of 10x).

    Article Snippet: Cell culturing reagents included: fetal bovine serum (FBS), DMEM:Ham’s F12 (1:1) (Invitrogen), 1x antibiotic-antimycotic (Invitrogen), anti-eGFP siRNA (sense: 5′-CAAGCUGACCCUGAAGUUCTT; anti-sense: 3′-GAACUUCAGGGUCAGCUUGCC), scrambled siRNA as a negative control (sense: 5′-AGUACUGCUUACGAUACGGTT; anti-sense: 3′-CCGUAUCGUAAGCAGUACUTT), plasmid enhanced green fluorescent protein DNA (eGFP-N1; referred to as eGFP) (Clontech), amplified and purified by Aldevron, pDsRed-Max-N1 DNA (dsRed) (Addgene), and CellTiter 96® AQueous One Solution Cell Proliferation Assay (Promega).

    Techniques: Fluorescence, Microscopy, Expressing, Transfection