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retroviral vector pmscv  (Addgene inc)


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    Structured Review

    Addgene inc retroviral vector pmscv
    Design of human/murine hybrid epidermal growth factor receptor (EGFR) and EGFR murine chimeric antigen receptor (CAR). ( A ) Schematic of the human/murine hybrid EGFR with cetuximab-binding substitutions (G442S, R467K, M491I, N492S, K497N) and its engagement by a cetuximab-derived single-chain variable fragment (scFv) on mCAR T cells. ( B ) The <t>retroviral</t> vector encoding the EGFR-specific murine CAR and green fluorescent protein (GFP); I—domain I; II—domain II; III—domain III; IV—domain IV.
    Retroviral Vector Pmscv, supplied by Addgene inc, used in various techniques. Bioz Stars score: 95/100, based on 150 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pmscv+retroviral+vector/MSCV-IRES-GFP+(Plasmid+%2320672)/pmc12785862-166-31-39
    Average 95 stars, based on 150 article reviews
    retroviral vector pmscv - by Bioz Stars, 2026-10
    95/100 stars

    Images

    1) Product Images from "Pre-Treatment with Dacarbazine Sensitizes B16 Melanoma to CAR T Cell Therapy in Syngeneic Mouse Model"

    Article Title: Pre-Treatment with Dacarbazine Sensitizes B16 Melanoma to CAR T Cell Therapy in Syngeneic Mouse Model

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms27010189

    Design of human/murine hybrid epidermal growth factor receptor (EGFR) and EGFR murine chimeric antigen receptor (CAR). ( A ) Schematic of the human/murine hybrid EGFR with cetuximab-binding substitutions (G442S, R467K, M491I, N492S, K497N) and its engagement by a cetuximab-derived single-chain variable fragment (scFv) on mCAR T cells. ( B ) The retroviral vector encoding the EGFR-specific murine CAR and green fluorescent protein (GFP); I—domain I; II—domain II; III—domain III; IV—domain IV.
    Figure Legend Snippet: Design of human/murine hybrid epidermal growth factor receptor (EGFR) and EGFR murine chimeric antigen receptor (CAR). ( A ) Schematic of the human/murine hybrid EGFR with cetuximab-binding substitutions (G442S, R467K, M491I, N492S, K497N) and its engagement by a cetuximab-derived single-chain variable fragment (scFv) on mCAR T cells. ( B ) The retroviral vector encoding the EGFR-specific murine CAR and green fluorescent protein (GFP); I—domain I; II—domain II; III—domain III; IV—domain IV.

    Techniques Used: Binding Assay, Derivative Assay, Retroviral, Plasmid Preparation

    Generation of murine EGFR CAR T cells. ( A ) Workflow for EGFR mCAR T cell production, including T cell isolation, activation, retroviral transduction, and subsequent in vitro and in vivo experiments created with BioRender ( https://www.biorender.com/ (accessed on 1 September 2025)). ( B ) Representative flow cytometry histogram showing the transduction efficiency of murine T cells with the EGFR-targeted murine CAR construct. ( C ) Summary of independent transduction preparations: percentage of GFP + cells in each preparation. ( D ) Expansion ( left ) and viability ( right ) of EGFR mCAR T cells compared to non-transduced T cells over 14 days of culture. * p < 0.05 and *** p < 0.001.
    Figure Legend Snippet: Generation of murine EGFR CAR T cells. ( A ) Workflow for EGFR mCAR T cell production, including T cell isolation, activation, retroviral transduction, and subsequent in vitro and in vivo experiments created with BioRender ( https://www.biorender.com/ (accessed on 1 September 2025)). ( B ) Representative flow cytometry histogram showing the transduction efficiency of murine T cells with the EGFR-targeted murine CAR construct. ( C ) Summary of independent transduction preparations: percentage of GFP + cells in each preparation. ( D ) Expansion ( left ) and viability ( right ) of EGFR mCAR T cells compared to non-transduced T cells over 14 days of culture. * p < 0.05 and *** p < 0.001.

    Techniques Used: Cell Isolation, Activation Assay, Retroviral, Transduction, In Vitro, In Vivo, Flow Cytometry, Construct

    Related Articles

    Over Expression:

    Article Title: The volume regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling
    Article Snippet: .. For overexpression of murine LRRC8C (Dharmacon, MMM1013–202767571) and p53 (Sino Biological, MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, 52114); empty pMSCV was used as control. ..

    Article Title: The volume-regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling.
    Article Snippet: For overexpression of murine LRRC8C (Dharmacon, catalog no. MMM1013202767571) and p53 (Sino Biological, catalog no. MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, catalog no. 52114); empty pMSCV was used as control. .. For overexpression of murine LRRC8C (Dharmacon, catalog no. MMM1013202767571) and p53 (Sino Biological, catalog no. MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, catalog no. 52114); empty pMSCV was used as control. ..

    Retroviral:

    Article Title: The volume regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling
    Article Snippet: .. For overexpression of murine LRRC8C (Dharmacon, MMM1013–202767571) and p53 (Sino Biological, MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, 52114); empty pMSCV was used as control. ..

    Article Title: The volume-regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling.
    Article Snippet: For overexpression of murine LRRC8C (Dharmacon, catalog no. MMM1013202767571) and p53 (Sino Biological, catalog no. MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, catalog no. 52114); empty pMSCV was used as control. .. For overexpression of murine LRRC8C (Dharmacon, catalog no. MMM1013202767571) and p53 (Sino Biological, catalog no. MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, catalog no. 52114); empty pMSCV was used as control. ..

    Article Title: Oncoprotein SET-associated transcription factor ZBTB11 triggers lung cancer metastasis
    Article Snippet: .. Mammalian expression constructs, including SET, ZBTB11, MMP9, and PRRG2, were generated by cloning each cDNA into a modified pIRESneo2 vector (Clontech, 6938-1), a pCMV-myc vector (Clontech, 635689), an SFB-NT or -CT destination vector (Gifted by Dr. Wenqi Wang, University of California Irvine), a pBabe retrovirus vector (Addgene, 1764) or a pMSCV retroviral vector (Addgene, 75085). ..

    Article Title: Inhibiting migration of cancer cells
    Article Snippet: A vector containing Nnat coding sequence and 3′-UTR was purchased from Origene (Cat#SC126815, Origene, Md.). .. To generate Nnat-mut, the miR-708 binding site was mutated in the Nnat 3′-UTR and cloned it into the pMSCV retroviral vector (Addgene, MA). .. To generate breast cancer cells stably expressing miRNAs, cells were transduced with lentivirus and sorted by flow cytometry (Aria II, BD Bioscience) to obtain stable cell lines.

    Plasmid Preparation:

    Article Title: The volume regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling
    Article Snippet: .. For overexpression of murine LRRC8C (Dharmacon, MMM1013–202767571) and p53 (Sino Biological, MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, 52114); empty pMSCV was used as control. ..

    Article Title: Oncoprotein SET-associated transcription factor ZBTB11 triggers lung cancer metastasis
    Article Snippet: .. Mammalian expression constructs, including SET, ZBTB11, MMP9, and PRRG2, were generated by cloning each cDNA into a modified pIRESneo2 vector (Clontech, 6938-1), a pCMV-myc vector (Clontech, 635689), an SFB-NT or -CT destination vector (Gifted by Dr. Wenqi Wang, University of California Irvine), a pBabe retrovirus vector (Addgene, 1764) or a pMSCV retroviral vector (Addgene, 75085). ..

    Control:

    Article Title: The volume regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling
    Article Snippet: .. For overexpression of murine LRRC8C (Dharmacon, MMM1013–202767571) and p53 (Sino Biological, MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, 52114); empty pMSCV was used as control. ..

    Article Title: The volume-regulated anion channel LRRC8C suppresses T cell function by regulating cyclic dinucleotide transport and STING-p53 signaling.
    Article Snippet: For overexpression of murine LRRC8C (Dharmacon, catalog no. MMM1013202767571) and p53 (Sino Biological, catalog no. MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, catalog no. 52114); empty pMSCV was used as control. .. For overexpression of murine LRRC8C (Dharmacon, catalog no. MMM1013202767571) and p53 (Sino Biological, catalog no. MG50534-UT), cDNAs were subcloned into the pMSCV retroviral vector (Addgene, catalog no. 52114); empty pMSCV was used as control. ..

    Expressing:

    Article Title: Oncoprotein SET-associated transcription factor ZBTB11 triggers lung cancer metastasis
    Article Snippet: .. Mammalian expression constructs, including SET, ZBTB11, MMP9, and PRRG2, were generated by cloning each cDNA into a modified pIRESneo2 vector (Clontech, 6938-1), a pCMV-myc vector (Clontech, 635689), an SFB-NT or -CT destination vector (Gifted by Dr. Wenqi Wang, University of California Irvine), a pBabe retrovirus vector (Addgene, 1764) or a pMSCV retroviral vector (Addgene, 75085). ..

    Construct:

    Article Title: Oncoprotein SET-associated transcription factor ZBTB11 triggers lung cancer metastasis
    Article Snippet: .. Mammalian expression constructs, including SET, ZBTB11, MMP9, and PRRG2, were generated by cloning each cDNA into a modified pIRESneo2 vector (Clontech, 6938-1), a pCMV-myc vector (Clontech, 635689), an SFB-NT or -CT destination vector (Gifted by Dr. Wenqi Wang, University of California Irvine), a pBabe retrovirus vector (Addgene, 1764) or a pMSCV retroviral vector (Addgene, 75085). ..

    Generated:

    Article Title: Oncoprotein SET-associated transcription factor ZBTB11 triggers lung cancer metastasis
    Article Snippet: .. Mammalian expression constructs, including SET, ZBTB11, MMP9, and PRRG2, were generated by cloning each cDNA into a modified pIRESneo2 vector (Clontech, 6938-1), a pCMV-myc vector (Clontech, 635689), an SFB-NT or -CT destination vector (Gifted by Dr. Wenqi Wang, University of California Irvine), a pBabe retrovirus vector (Addgene, 1764) or a pMSCV retroviral vector (Addgene, 75085). ..

    Cloning:

    Article Title: Oncoprotein SET-associated transcription factor ZBTB11 triggers lung cancer metastasis
    Article Snippet: .. Mammalian expression constructs, including SET, ZBTB11, MMP9, and PRRG2, were generated by cloning each cDNA into a modified pIRESneo2 vector (Clontech, 6938-1), a pCMV-myc vector (Clontech, 635689), an SFB-NT or -CT destination vector (Gifted by Dr. Wenqi Wang, University of California Irvine), a pBabe retrovirus vector (Addgene, 1764) or a pMSCV retroviral vector (Addgene, 75085). ..

    Modification:

    Article Title: Oncoprotein SET-associated transcription factor ZBTB11 triggers lung cancer metastasis
    Article Snippet: .. Mammalian expression constructs, including SET, ZBTB11, MMP9, and PRRG2, were generated by cloning each cDNA into a modified pIRESneo2 vector (Clontech, 6938-1), a pCMV-myc vector (Clontech, 635689), an SFB-NT or -CT destination vector (Gifted by Dr. Wenqi Wang, University of California Irvine), a pBabe retrovirus vector (Addgene, 1764) or a pMSCV retroviral vector (Addgene, 75085). ..

    Binding Assay:

    Article Title: Inhibiting migration of cancer cells
    Article Snippet: A vector containing Nnat coding sequence and 3′-UTR was purchased from Origene (Cat#SC126815, Origene, Md.). .. To generate Nnat-mut, the miR-708 binding site was mutated in the Nnat 3′-UTR and cloned it into the pMSCV retroviral vector (Addgene, MA). .. To generate breast cancer cells stably expressing miRNAs, cells were transduced with lentivirus and sorted by flow cytometry (Aria II, BD Bioscience) to obtain stable cell lines.

    Clone Assay:

    Article Title: Inhibiting migration of cancer cells
    Article Snippet: A vector containing Nnat coding sequence and 3′-UTR was purchased from Origene (Cat#SC126815, Origene, Md.). .. To generate Nnat-mut, the miR-708 binding site was mutated in the Nnat 3′-UTR and cloned it into the pMSCV retroviral vector (Addgene, MA). .. To generate breast cancer cells stably expressing miRNAs, cells were transduced with lentivirus and sorted by flow cytometry (Aria II, BD Bioscience) to obtain stable cell lines.



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    Image Search Results


    Design of human/murine hybrid epidermal growth factor receptor (EGFR) and EGFR murine chimeric antigen receptor (CAR). ( A ) Schematic of the human/murine hybrid EGFR with cetuximab-binding substitutions (G442S, R467K, M491I, N492S, K497N) and its engagement by a cetuximab-derived single-chain variable fragment (scFv) on mCAR T cells. ( B ) The retroviral vector encoding the EGFR-specific murine CAR and green fluorescent protein (GFP); I—domain I; II—domain II; III—domain III; IV—domain IV.

    Journal: International Journal of Molecular Sciences

    Article Title: Pre-Treatment with Dacarbazine Sensitizes B16 Melanoma to CAR T Cell Therapy in Syngeneic Mouse Model

    doi: 10.3390/ijms27010189

    Figure Lengend Snippet: Design of human/murine hybrid epidermal growth factor receptor (EGFR) and EGFR murine chimeric antigen receptor (CAR). ( A ) Schematic of the human/murine hybrid EGFR with cetuximab-binding substitutions (G442S, R467K, M491I, N492S, K497N) and its engagement by a cetuximab-derived single-chain variable fragment (scFv) on mCAR T cells. ( B ) The retroviral vector encoding the EGFR-specific murine CAR and green fluorescent protein (GFP); I—domain I; II—domain II; III—domain III; IV—domain IV.

    Article Snippet: The synthetic CAR gene was cloned by PCR amplification with primers containing restriction sites, restriction digest, and ligation (restriction enzymes and ligase from New England Biolabs, Ipswich, MA, USA) into the retroviral vector pMSCV (a gift from Dr. Reya, Addgene, #20672) right before IRES followed by the reporter gene of GFP.

    Techniques: Binding Assay, Derivative Assay, Retroviral, Plasmid Preparation

    Generation of murine EGFR CAR T cells. ( A ) Workflow for EGFR mCAR T cell production, including T cell isolation, activation, retroviral transduction, and subsequent in vitro and in vivo experiments created with BioRender ( https://www.biorender.com/ (accessed on 1 September 2025)). ( B ) Representative flow cytometry histogram showing the transduction efficiency of murine T cells with the EGFR-targeted murine CAR construct. ( C ) Summary of independent transduction preparations: percentage of GFP + cells in each preparation. ( D ) Expansion ( left ) and viability ( right ) of EGFR mCAR T cells compared to non-transduced T cells over 14 days of culture. * p < 0.05 and *** p < 0.001.

    Journal: International Journal of Molecular Sciences

    Article Title: Pre-Treatment with Dacarbazine Sensitizes B16 Melanoma to CAR T Cell Therapy in Syngeneic Mouse Model

    doi: 10.3390/ijms27010189

    Figure Lengend Snippet: Generation of murine EGFR CAR T cells. ( A ) Workflow for EGFR mCAR T cell production, including T cell isolation, activation, retroviral transduction, and subsequent in vitro and in vivo experiments created with BioRender ( https://www.biorender.com/ (accessed on 1 September 2025)). ( B ) Representative flow cytometry histogram showing the transduction efficiency of murine T cells with the EGFR-targeted murine CAR construct. ( C ) Summary of independent transduction preparations: percentage of GFP + cells in each preparation. ( D ) Expansion ( left ) and viability ( right ) of EGFR mCAR T cells compared to non-transduced T cells over 14 days of culture. * p < 0.05 and *** p < 0.001.

    Article Snippet: The synthetic CAR gene was cloned by PCR amplification with primers containing restriction sites, restriction digest, and ligation (restriction enzymes and ligase from New England Biolabs, Ipswich, MA, USA) into the retroviral vector pMSCV (a gift from Dr. Reya, Addgene, #20672) right before IRES followed by the reporter gene of GFP.

    Techniques: Cell Isolation, Activation Assay, Retroviral, Transduction, In Vitro, In Vivo, Flow Cytometry, Construct

    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