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plasmids pcag ires gfp control vector  (Addgene inc)


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    Addgene inc plasmids pcag ires gfp control vector
    Transfection of NSPCs with a Ngn2 cDNA induces neuronal differentiation. Cells were cultured for 5 days in differentiation medium. A, NSPCs derived from APPKO mice were transfected either with empty vector <t>pCAG-IRES-GFP</t> (Control) or with pCAG-Ngn2-IRES-GFP (Ngn2). The figure shows 3 independent representative immunofluorescence images for each group. Transfected cells (green) are marked with asterisks. Cells were stained for β-III-tubulin (red). No double-stained GFP+ β-III-tubulin+ cells were observed in empty vector incubation, indicating that cells transfected with the empty vector are not neurons. In cells transfected with the Ngn2 plasmid, there was co-staining of GFP and β-III-tubulin, indicating that each cell transfected with Ngn2 was neuronally differentiated. B, quantification of the results in panel A shows the % of β-III-tubulin+ GFP+ cells to total GFP+ cells. C, representative immunofluorescence images of NSPCs derived from WT mice transfected with siRNA-control-Cy3 vector or siRNA-Ngn2-Cy3 vector (Ngn2). The figure shows siRNA (red), β-III-tubulin (green), and DAPI (blue) staining. Cells transfected with the control plasmid (61) showed co-staining of siRNA and β-III-tubulin. Cells transfected with the Ngn2 siRNA (Ngn2), marked with arrows, were not β-III-tubulin+ (asterisk). D, quantification of the results in C showing the % β-III-tubulin+ siRNA+ cells to total siRNA+ cells. F, western blotting analysis of Ngn2 levels. The figure shows a representative western blot (E) and quantification (F). Decreased expression of Ngn2 was observed in NSPCs after siRNA interference. Cells were cultured for 5 days in differentiation medium. β-Actin was used as a control for protein loading. Scale bars = 50 μm. Data are expressed as the means ± S.E. (** = p < 0.001; *** = p < 0.0001 as determined by Student's t test). Cont, control; Ngn2, neurogenin 2.
    Plasmids Pcag Ires Gfp Control Vector, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/plasmids pcag ires gfp control vector/product/Addgene inc
    Average 93 stars, based on 3 article reviews
    plasmids pcag ires gfp control vector - by Bioz Stars, 2026-02
    93/100 stars

    Images

    1) Product Images from "Neurogenin 2 Mediates Amyloid-β Precursor Protein-stimulated Neurogenesis * "

    Article Title: Neurogenin 2 Mediates Amyloid-β Precursor Protein-stimulated Neurogenesis *

    Journal: The Journal of Biological Chemistry

    doi: 10.1074/jbc.M114.581918

    Transfection of NSPCs with a Ngn2 cDNA induces neuronal differentiation. Cells were cultured for 5 days in differentiation medium. A, NSPCs derived from APPKO mice were transfected either with empty vector pCAG-IRES-GFP (Control) or with pCAG-Ngn2-IRES-GFP (Ngn2). The figure shows 3 independent representative immunofluorescence images for each group. Transfected cells (green) are marked with asterisks. Cells were stained for β-III-tubulin (red). No double-stained GFP+ β-III-tubulin+ cells were observed in empty vector incubation, indicating that cells transfected with the empty vector are not neurons. In cells transfected with the Ngn2 plasmid, there was co-staining of GFP and β-III-tubulin, indicating that each cell transfected with Ngn2 was neuronally differentiated. B, quantification of the results in panel A shows the % of β-III-tubulin+ GFP+ cells to total GFP+ cells. C, representative immunofluorescence images of NSPCs derived from WT mice transfected with siRNA-control-Cy3 vector or siRNA-Ngn2-Cy3 vector (Ngn2). The figure shows siRNA (red), β-III-tubulin (green), and DAPI (blue) staining. Cells transfected with the control plasmid (61) showed co-staining of siRNA and β-III-tubulin. Cells transfected with the Ngn2 siRNA (Ngn2), marked with arrows, were not β-III-tubulin+ (asterisk). D, quantification of the results in C showing the % β-III-tubulin+ siRNA+ cells to total siRNA+ cells. F, western blotting analysis of Ngn2 levels. The figure shows a representative western blot (E) and quantification (F). Decreased expression of Ngn2 was observed in NSPCs after siRNA interference. Cells were cultured for 5 days in differentiation medium. β-Actin was used as a control for protein loading. Scale bars = 50 μm. Data are expressed as the means ± S.E. (** = p < 0.001; *** = p < 0.0001 as determined by Student's t test). Cont, control; Ngn2, neurogenin 2.
    Figure Legend Snippet: Transfection of NSPCs with a Ngn2 cDNA induces neuronal differentiation. Cells were cultured for 5 days in differentiation medium. A, NSPCs derived from APPKO mice were transfected either with empty vector pCAG-IRES-GFP (Control) or with pCAG-Ngn2-IRES-GFP (Ngn2). The figure shows 3 independent representative immunofluorescence images for each group. Transfected cells (green) are marked with asterisks. Cells were stained for β-III-tubulin (red). No double-stained GFP+ β-III-tubulin+ cells were observed in empty vector incubation, indicating that cells transfected with the empty vector are not neurons. In cells transfected with the Ngn2 plasmid, there was co-staining of GFP and β-III-tubulin, indicating that each cell transfected with Ngn2 was neuronally differentiated. B, quantification of the results in panel A shows the % of β-III-tubulin+ GFP+ cells to total GFP+ cells. C, representative immunofluorescence images of NSPCs derived from WT mice transfected with siRNA-control-Cy3 vector or siRNA-Ngn2-Cy3 vector (Ngn2). The figure shows siRNA (red), β-III-tubulin (green), and DAPI (blue) staining. Cells transfected with the control plasmid (61) showed co-staining of siRNA and β-III-tubulin. Cells transfected with the Ngn2 siRNA (Ngn2), marked with arrows, were not β-III-tubulin+ (asterisk). D, quantification of the results in C showing the % β-III-tubulin+ siRNA+ cells to total siRNA+ cells. F, western blotting analysis of Ngn2 levels. The figure shows a representative western blot (E) and quantification (F). Decreased expression of Ngn2 was observed in NSPCs after siRNA interference. Cells were cultured for 5 days in differentiation medium. β-Actin was used as a control for protein loading. Scale bars = 50 μm. Data are expressed as the means ± S.E. (** = p < 0.001; *** = p < 0.0001 as determined by Student's t test). Cont, control; Ngn2, neurogenin 2.

    Techniques Used: Transfection, Cell Culture, Derivative Assay, Plasmid Preparation, Immunofluorescence, Staining, Incubation, Western Blot, Expressing



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    plasmids pcag ires gfp control vector  (Addgene inc)
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    Addgene inc plasmids pcag ires gfp control vector
    Transfection of NSPCs with a Ngn2 cDNA induces neuronal differentiation. Cells were cultured for 5 days in differentiation medium. A, NSPCs derived from APPKO mice were transfected either with empty vector <t>pCAG-IRES-GFP</t> (Control) or with pCAG-Ngn2-IRES-GFP (Ngn2). The figure shows 3 independent representative immunofluorescence images for each group. Transfected cells (green) are marked with asterisks. Cells were stained for β-III-tubulin (red). No double-stained GFP+ β-III-tubulin+ cells were observed in empty vector incubation, indicating that cells transfected with the empty vector are not neurons. In cells transfected with the Ngn2 plasmid, there was co-staining of GFP and β-III-tubulin, indicating that each cell transfected with Ngn2 was neuronally differentiated. B, quantification of the results in panel A shows the % of β-III-tubulin+ GFP+ cells to total GFP+ cells. C, representative immunofluorescence images of NSPCs derived from WT mice transfected with siRNA-control-Cy3 vector or siRNA-Ngn2-Cy3 vector (Ngn2). The figure shows siRNA (red), β-III-tubulin (green), and DAPI (blue) staining. Cells transfected with the control plasmid (61) showed co-staining of siRNA and β-III-tubulin. Cells transfected with the Ngn2 siRNA (Ngn2), marked with arrows, were not β-III-tubulin+ (asterisk). D, quantification of the results in C showing the % β-III-tubulin+ siRNA+ cells to total siRNA+ cells. F, western blotting analysis of Ngn2 levels. The figure shows a representative western blot (E) and quantification (F). Decreased expression of Ngn2 was observed in NSPCs after siRNA interference. Cells were cultured for 5 days in differentiation medium. β-Actin was used as a control for protein loading. Scale bars = 50 μm. Data are expressed as the means ± S.E. (** = p < 0.001; *** = p < 0.0001 as determined by Student's t test). Cont, control; Ngn2, neurogenin 2.
    Plasmids Pcag Ires Gfp Control Vector, 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/plasmids pcag ires gfp control vector/product/Addgene inc
    Average 93 stars, based on 1 article reviews
    plasmids pcag ires gfp control vector - by Bioz Stars, 2026-02
    93/100 stars
    		  Buy from Supplier

    Image Search Results


    Transfection of NSPCs with a Ngn2 cDNA induces neuronal differentiation. Cells were cultured for 5 days in differentiation medium. A, NSPCs derived from APPKO mice were transfected either with empty vector pCAG-IRES-GFP (Control) or with pCAG-Ngn2-IRES-GFP (Ngn2). The figure shows 3 independent representative immunofluorescence images for each group. Transfected cells (green) are marked with asterisks. Cells were stained for β-III-tubulin (red). No double-stained GFP+ β-III-tubulin+ cells were observed in empty vector incubation, indicating that cells transfected with the empty vector are not neurons. In cells transfected with the Ngn2 plasmid, there was co-staining of GFP and β-III-tubulin, indicating that each cell transfected with Ngn2 was neuronally differentiated. B, quantification of the results in panel A shows the % of β-III-tubulin+ GFP+ cells to total GFP+ cells. C, representative immunofluorescence images of NSPCs derived from WT mice transfected with siRNA-control-Cy3 vector or siRNA-Ngn2-Cy3 vector (Ngn2). The figure shows siRNA (red), β-III-tubulin (green), and DAPI (blue) staining. Cells transfected with the control plasmid (61) showed co-staining of siRNA and β-III-tubulin. Cells transfected with the Ngn2 siRNA (Ngn2), marked with arrows, were not β-III-tubulin+ (asterisk). D, quantification of the results in C showing the % β-III-tubulin+ siRNA+ cells to total siRNA+ cells. F, western blotting analysis of Ngn2 levels. The figure shows a representative western blot (E) and quantification (F). Decreased expression of Ngn2 was observed in NSPCs after siRNA interference. Cells were cultured for 5 days in differentiation medium. β-Actin was used as a control for protein loading. Scale bars = 50 μm. Data are expressed as the means ± S.E. (** = p < 0.001; *** = p < 0.0001 as determined by Student's t test). Cont, control; Ngn2, neurogenin 2.

    Journal: The Journal of Biological Chemistry

    Article Title: Neurogenin 2 Mediates Amyloid-β Precursor Protein-stimulated Neurogenesis *

    doi: 10.1074/jbc.M114.581918

    Figure Lengend Snippet: Transfection of NSPCs with a Ngn2 cDNA induces neuronal differentiation. Cells were cultured for 5 days in differentiation medium. A, NSPCs derived from APPKO mice were transfected either with empty vector pCAG-IRES-GFP (Control) or with pCAG-Ngn2-IRES-GFP (Ngn2). The figure shows 3 independent representative immunofluorescence images for each group. Transfected cells (green) are marked with asterisks. Cells were stained for β-III-tubulin (red). No double-stained GFP+ β-III-tubulin+ cells were observed in empty vector incubation, indicating that cells transfected with the empty vector are not neurons. In cells transfected with the Ngn2 plasmid, there was co-staining of GFP and β-III-tubulin, indicating that each cell transfected with Ngn2 was neuronally differentiated. B, quantification of the results in panel A shows the % of β-III-tubulin+ GFP+ cells to total GFP+ cells. C, representative immunofluorescence images of NSPCs derived from WT mice transfected with siRNA-control-Cy3 vector or siRNA-Ngn2-Cy3 vector (Ngn2). The figure shows siRNA (red), β-III-tubulin (green), and DAPI (blue) staining. Cells transfected with the control plasmid (61) showed co-staining of siRNA and β-III-tubulin. Cells transfected with the Ngn2 siRNA (Ngn2), marked with arrows, were not β-III-tubulin+ (asterisk). D, quantification of the results in C showing the % β-III-tubulin+ siRNA+ cells to total siRNA+ cells. F, western blotting analysis of Ngn2 levels. The figure shows a representative western blot (E) and quantification (F). Decreased expression of Ngn2 was observed in NSPCs after siRNA interference. Cells were cultured for 5 days in differentiation medium. β-Actin was used as a control for protein loading. Scale bars = 50 μm. Data are expressed as the means ± S.E. (** = p < 0.001; *** = p < 0.0001 as determined by Student's t test). Cont, control; Ngn2, neurogenin 2.

    Article Snippet: Plasmid pCAG-Ngn2-IRES-GFP for the expression of Ngn2 was a kind gift of François Guillemot (MRC-National Institute for Medical Research, London, UK), and the plasmids pCAG-IRES-GFP control vector and pCAG-IRES-APP695 were from Addgene (Cambridge, MA).

    Techniques: Transfection, Cell Culture, Derivative Assay, Plasmid Preparation, Immunofluorescence, Staining, Incubation, Western Blot, Expressing