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retroviral vector pmscv ires gfp ii  (Addgene inc)


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    Addgene inc retroviral vector pmscv ires gfp ii
    Retroviral Vector Pmscv Ires Gfp Ii, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 98 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pmig+vectors/bio_rxiv__2025__11__05__686789-320-12-18?v=Addgene+inc
    Average 94 stars, based on 98 article reviews
    retroviral vector pmscv ires gfp ii - by Bioz Stars, 2026-07
    94/100 stars

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    New England Biolabs pmscv ires gfp retroviral vector pmig
    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after <t>retroviral</t> transduction with <t>pMIG</t> empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.
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    Addgene inc retroviral vector pmscv ires gfp ii
    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after <t>retroviral</t> transduction with <t>pMIG</t> empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.
    Retroviral Vector Pmscv Ires Gfp Ii, supplied by Addgene inc, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Addgene inc retroviral vector pmig
    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after <t>retroviral</t> transduction with <t>pMIG</t> empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.
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    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after <t>retroviral</t> transduction with <t>pMIG</t> empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.
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    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after <t>retroviral</t> transduction with <t>pMIG</t> empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.
    Pmscv Ires Gfp Pmig Retroviral 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
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    Addgene inc pmig ii vector 80
    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after <t>retroviral</t> transduction with <t>pMIG</t> empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.
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    Addgene inc pmscv ires mcherry vectors
    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after <t>retroviral</t> transduction with <t>pMIG</t> empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.
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    Addgene inc pmscv ires gfp empty vector
    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after <t>retroviral</t> transduction with <t>pMIG</t> empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.
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    Addgene inc retroviral vector pmig flag mll af9
    (A) Experimental schematic of <t>MLL-AF9</t> AML model. (B) Survival of mice transplanted with MLL-AF9 leukemia (WT- MLL-AF9 , n = 9; Erg +/- - MLL-AF9 , n =10). (C) CD11b MFI from spleen at the endpoint (WT- MLL-AF9 , n = 7; Erg +/- - MLL-AF9 , n = 3). Statistical tests were Log-rank test (B) or unpaired Student’s t test (C); ** P < 0.01.
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    Image Search Results


    a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after retroviral transduction with pMIG empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.

    Journal: Cell Death & Disease

    Article Title: IL-6-C/EBPβ signaling drives monocytic differentiation of murine cultured lymphoid progenitors with immunoregulatory properties

    doi: 10.1038/s41419-025-07930-4

    Figure Lengend Snippet: a Scatter plot of DEG (FDR < 0.05, >2-fold or <0.5- fold) between undifferentiated cCLPs and cCLPs after 24 h incubation with FL/SCF/IL-6 (D1). b Venn diagram of genes up-regulated in D1 to cCLPs with enrichment analysis of “Cell Differentiation” by GO Biological process and those up-regulated in D3 to cCLPs. c Heatmap view of 57 genes overlapped in ( b ). Color code values indicate the Z-score for each gene across samples. d Gene expression of Cebpb ( left panel ) and Id1 ( right panel ) in indicated samples. The values are shown as log 2 (CPM + 4) from RNA-seq data. e Representative FACS plots of cCLP-Ms differentiated from single cCLP clones where indicated genes were targeted by Crispr/Cas9. The name of a representative clone targeted to each gene is shown (#2–3, #2-17, #2-16). f Frequency of wells with more than 100 live cells in ( e ). g Frequency of wells with less than 40% CD11b + CD115 + cells. h Representative histogram of GFP expression ( left panels) , plots for CD11b and CD115 expression on GFP - gate ( middle panels ), or GFP + gate ( right panels ) in cCLPs on day 4 after retroviral transduction with pMIG empty vector ( upper panels ) or pMIG/ C/EBPβ ( lower panels ). i Percentages of CD11b + CD115 + cells in the indicated fractions in ( h ). Data are mean ± SD with statistical significance determined by one-way ANOVA (in d ) or two-way ANOVA (in i ) with multiple comparisons. The p values are represented as **, <0.01; ***, <0.001; ****, <0.0001. n.s. not significant.

    Article Snippet: The amplified PCR product was inserted at the Xho I site of the pMSCV-IRES-GFP retroviral vector (pMIG) using NEBuilder HiFi DNA Assembly Master Mix (New England Biolabs, E2621S).

    Techniques: Incubation, Cell Differentiation, Gene Expression, RNA Sequencing, Clone Assay, CRISPR, Expressing, Retroviral, Transduction, Plasmid Preparation

    (A) Experimental schematic of MLL-AF9 AML model. (B) Survival of mice transplanted with MLL-AF9 leukemia (WT- MLL-AF9 , n = 9; Erg +/- - MLL-AF9 , n =10). (C) CD11b MFI from spleen at the endpoint (WT- MLL-AF9 , n = 7; Erg +/- - MLL-AF9 , n = 3). Statistical tests were Log-rank test (B) or unpaired Student’s t test (C); ** P < 0.01.

    Journal: bioRxiv

    Article Title: Dynamic activity of Erg promotes aging of the hematopoietic system

    doi: 10.1101/2025.01.23.634563

    Figure Lengend Snippet: (A) Experimental schematic of MLL-AF9 AML model. (B) Survival of mice transplanted with MLL-AF9 leukemia (WT- MLL-AF9 , n = 9; Erg +/- - MLL-AF9 , n =10). (C) CD11b MFI from spleen at the endpoint (WT- MLL-AF9 , n = 7; Erg +/- - MLL-AF9 , n = 3). Statistical tests were Log-rank test (B) or unpaired Student’s t test (C); ** P < 0.01.

    Article Snippet: The retroviral vector pMIG-FLAG-MLL-AF9 (Addgene #71443) and pCL-Eco (Addgene #12371) were used for transfection to generate retrovirus .

    Techniques: