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virus strains encephalomyocarditis virus emcv atcc  (ATCC)


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    ATCC virus strains encephalomyocarditis virus emcv atcc
    Virus Strains Encephalomyocarditis Virus Emcv Atcc, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 205 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 95 stars, based on 205 article reviews
    virus strains encephalomyocarditis virus emcv atcc - by Bioz Stars, 2026-05
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    Thermo Fisher cdna emcv vr-129b strain
    Generation of the recombinant <t>EMCV</t> (class II IRES). (A) A schematic representation of the EMCV genome and the gene fragments prepared. A total of six fragments were amplified and then assembled with the new UTR linker fragment by CPER. Gel electrophoresis analysis was conducted to confirm the size of the six PCR amplicons (left panel). PCR assembly was used to connect neighboring fragments and the size of joined fragments was assessed by gel electrophoresis (right panel). F: fragment; M: 1 kb DNA ladder. (B) Huh7 cells were inoculated with 100 µL of culture supernatants collected from CPER-transfected cells. At 8 hpi, the cells were subjected to immunofluorescent staining of double-stranded RNA (dsRNA; green). Nuclei were counterstained with DAPI (blue). Scale bars, 25 µm. (C) Huh7 cells were inoculated with recombinant EMCV at an MOI of 0.01. The virus titers in supernatants and intracellular viral RNA were determined at the indicated timepoints by plaque-forming assay and qRT-PCR, respectively. (D) Both linkers were individually subjected to CPER assembly to evaluate the efficiency of recovery of recombinant EMCV as measured by a plaque-forming assay (bar graph). Asterisks indicate significant differences (*P < 0.05) versus the results of the CMV promoter. ND: not detected. Assays were performed independently in triplicate (C, D).
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    HIF activation exerts broad antiviral activity in neuron-like cells (A and B) Virus titer of vesicular stomatitis virus (VSV) and <t>encephalomyocarditis</t> <t>virus</t> <t>(EMCV)</t> in culture supernatants from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 19 h with EMCV (MOI 0.1) or VSV (MOI 0.001). n = 3 biological replicates. (C) SARS-CoV-2 N2 RNA levels evaluated by RT-qPCR in total RNA from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 48 h with SARS-CoV-2 (MOI 1). Data were normalized against 18S rRNA. n = 5 biological replicates. (D) Influenza A virus M2 RNA levels evaluated by RT-qPCR in total RNA from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 24 h with influenza A virus (MOI 0.1). Data were normalized against 18S rRNA. n = 5 biological replicates. (E) Measles virus titer in culture supernatants from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 36 h with Measles virus (MOI 0.1). n = 6 biological replicates. Data are representative of at least three independent experiments. The data are shown as means ± SD. Individual values are represented by dots. For (A), Mann-Whitney was applied to identify statistical significance. For (B)–(E), the statistical analyses were performed by Student’s t test, two-tailed, parametric distribution to identify statistical significance. ns, not significant. Illustrations of viruses were generated with BioRender.
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    ATCC emcv strain pv21
    HIF activation exerts broad antiviral activity in neuron-like cells (A and B) Virus titer of vesicular stomatitis virus (VSV) and <t>encephalomyocarditis</t> <t>virus</t> <t>(EMCV)</t> in culture supernatants from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 19 h with EMCV (MOI 0.1) or VSV (MOI 0.001). n = 3 biological replicates. (C) SARS-CoV-2 N2 RNA levels evaluated by RT-qPCR in total RNA from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 48 h with SARS-CoV-2 (MOI 1). Data were normalized against 18S rRNA. n = 5 biological replicates. (D) Influenza A virus M2 RNA levels evaluated by RT-qPCR in total RNA from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 24 h with influenza A virus (MOI 0.1). Data were normalized against 18S rRNA. n = 5 biological replicates. (E) Measles virus titer in culture supernatants from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 36 h with Measles virus (MOI 0.1). n = 6 biological replicates. Data are representative of at least three independent experiments. The data are shown as means ± SD. Individual values are represented by dots. For (A), Mann-Whitney was applied to identify statistical significance. For (B)–(E), the statistical analyses were performed by Student’s t test, two-tailed, parametric distribution to identify statistical significance. ns, not significant. Illustrations of viruses were generated with BioRender.
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    Reagents and tools table

    Journal: EMBO Reports

    Article Title: Cholesterol restriction primes antiviral innate immunity via SREBP1-driven noncanonical type I IFNs

    doi: 10.1038/s44319-024-00346-9

    Figure Lengend Snippet: Reagents and tools table

    Article Snippet: EMCV , ATCC , VR-1762 strain.

    Techniques: Recombinant, Sequencing, CRISPR, Knock-Out, Cloning, Plasmid Preparation, Membrane, Protease Inhibitor, Software, Virus, Reporter Assay, Chromatin Immunoprecipitation, Magnetic Beads, Enzyme-linked Immunosorbent Assay

    Generation of the recombinant EMCV (class II IRES). (A) A schematic representation of the EMCV genome and the gene fragments prepared. A total of six fragments were amplified and then assembled with the new UTR linker fragment by CPER. Gel electrophoresis analysis was conducted to confirm the size of the six PCR amplicons (left panel). PCR assembly was used to connect neighboring fragments and the size of joined fragments was assessed by gel electrophoresis (right panel). F: fragment; M: 1 kb DNA ladder. (B) Huh7 cells were inoculated with 100 µL of culture supernatants collected from CPER-transfected cells. At 8 hpi, the cells were subjected to immunofluorescent staining of double-stranded RNA (dsRNA; green). Nuclei were counterstained with DAPI (blue). Scale bars, 25 µm. (C) Huh7 cells were inoculated with recombinant EMCV at an MOI of 0.01. The virus titers in supernatants and intracellular viral RNA were determined at the indicated timepoints by plaque-forming assay and qRT-PCR, respectively. (D) Both linkers were individually subjected to CPER assembly to evaluate the efficiency of recovery of recombinant EMCV as measured by a plaque-forming assay (bar graph). Asterisks indicate significant differences (*P < 0.05) versus the results of the CMV promoter. ND: not detected. Assays were performed independently in triplicate (C, D).

    Journal: Journal of Virology

    Article Title: A rapid and versatile reverse genetics approach for generating recombinant positive-strand RNA viruses that use IRES-mediated translation

    doi: 10.1128/jvi.01638-23

    Figure Lengend Snippet: Generation of the recombinant EMCV (class II IRES). (A) A schematic representation of the EMCV genome and the gene fragments prepared. A total of six fragments were amplified and then assembled with the new UTR linker fragment by CPER. Gel electrophoresis analysis was conducted to confirm the size of the six PCR amplicons (left panel). PCR assembly was used to connect neighboring fragments and the size of joined fragments was assessed by gel electrophoresis (right panel). F: fragment; M: 1 kb DNA ladder. (B) Huh7 cells were inoculated with 100 µL of culture supernatants collected from CPER-transfected cells. At 8 hpi, the cells were subjected to immunofluorescent staining of double-stranded RNA (dsRNA; green). Nuclei were counterstained with DAPI (blue). Scale bars, 25 µm. (C) Huh7 cells were inoculated with recombinant EMCV at an MOI of 0.01. The virus titers in supernatants and intracellular viral RNA were determined at the indicated timepoints by plaque-forming assay and qRT-PCR, respectively. (D) Both linkers were individually subjected to CPER assembly to evaluate the efficiency of recovery of recombinant EMCV as measured by a plaque-forming assay (bar graph). Asterisks indicate significant differences (*P < 0.05) versus the results of the CMV promoter. ND: not detected. Assays were performed independently in triplicate (C, D).

    Article Snippet: The cDNA EMCV VR-129B strain (GenBank accession number: KM269482 ) was synthesized by Thermo Fisher Scientific.

    Techniques: Recombinant, Amplification, Nucleic Acid Electrophoresis, Transfection, Staining, Virus, Quantitative RT-PCR

    HIF activation exerts broad antiviral activity in neuron-like cells (A and B) Virus titer of vesicular stomatitis virus (VSV) and encephalomyocarditis virus (EMCV) in culture supernatants from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 19 h with EMCV (MOI 0.1) or VSV (MOI 0.001). n = 3 biological replicates. (C) SARS-CoV-2 N2 RNA levels evaluated by RT-qPCR in total RNA from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 48 h with SARS-CoV-2 (MOI 1). Data were normalized against 18S rRNA. n = 5 biological replicates. (D) Influenza A virus M2 RNA levels evaluated by RT-qPCR in total RNA from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 24 h with influenza A virus (MOI 0.1). Data were normalized against 18S rRNA. n = 5 biological replicates. (E) Measles virus titer in culture supernatants from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 36 h with Measles virus (MOI 0.1). n = 6 biological replicates. Data are representative of at least three independent experiments. The data are shown as means ± SD. Individual values are represented by dots. For (A), Mann-Whitney was applied to identify statistical significance. For (B)–(E), the statistical analyses were performed by Student’s t test, two-tailed, parametric distribution to identify statistical significance. ns, not significant. Illustrations of viruses were generated with BioRender.

    Journal: Cell Reports

    Article Title: The HIF transcription network exerts innate antiviral activity in neurons and limits brain inflammation

    doi: 10.1016/j.celrep.2024.113792

    Figure Lengend Snippet: HIF activation exerts broad antiviral activity in neuron-like cells (A and B) Virus titer of vesicular stomatitis virus (VSV) and encephalomyocarditis virus (EMCV) in culture supernatants from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 19 h with EMCV (MOI 0.1) or VSV (MOI 0.001). n = 3 biological replicates. (C) SARS-CoV-2 N2 RNA levels evaluated by RT-qPCR in total RNA from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 48 h with SARS-CoV-2 (MOI 1). Data were normalized against 18S rRNA. n = 5 biological replicates. (D) Influenza A virus M2 RNA levels evaluated by RT-qPCR in total RNA from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 24 h with influenza A virus (MOI 0.1). Data were normalized against 18S rRNA. n = 5 biological replicates. (E) Measles virus titer in culture supernatants from SH-Sy5y cells treated with ML228 (0.5 μM) and infected for 36 h with Measles virus (MOI 0.1). n = 6 biological replicates. Data are representative of at least three independent experiments. The data are shown as means ± SD. Individual values are represented by dots. For (A), Mann-Whitney was applied to identify statistical significance. For (B)–(E), the statistical analyses were performed by Student’s t test, two-tailed, parametric distribution to identify statistical significance. ns, not significant. Illustrations of viruses were generated with BioRender.

    Article Snippet: EMCV (EMC) strain , ATCC , #VR-129B.

    Techniques: Activation Assay, Activity Assay, Virus, Infection, Quantitative RT-PCR, MANN-WHITNEY, Two Tailed Test, Generated

    Journal: Cell Reports

    Article Title: The HIF transcription network exerts innate antiviral activity in neurons and limits brain inflammation

    doi: 10.1016/j.celrep.2024.113792

    Figure Lengend Snippet:

    Article Snippet: EMCV (EMC) strain , ATCC , #VR-129B.

    Techniques: Virus, Variant Assay, Recombinant, Isolation, Extraction, SYBR Green Assay, Enzyme-linked Immunosorbent Assay, Sample Prep, Expressing, Software, Imaging, Modification, Knock-Out