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reference number atcc vr 118tm  (ATCC)


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    Structured Review

    ATCC reference number atcc vr 118tm
    Reference Number Atcc Vr 118tm, supplied by ATCC, used in various techniques. Bioz Stars score: 93/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/vr+118/Vaccinia+virus/us12364724-110-15-17
    Average 93 stars, based on 14 article reviews
    reference number atcc vr 118tm - by Bioz Stars, 2026-11
    93/100 stars

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    Related Articles

    Virus:

    Article Title: Smallpox vaccine for cancer treatment
    Article Snippet: .. In some embodiments, the NYCBOH strain of vaccinia virus may be ATCC VR-118 or CJ-MVB-SPX. ..

    Article Title: Smallpox vaccine for cancer treatment
    Article Snippet: .. In some embodiments, the NYCBOH strain of vaccinia virus may be ATCC VR-118 or CJ-MVB-SPX. ..

    Article Title: Enhanced systems for cell-mediated oncolytic viral therapy
    Article Snippet: .. In some embodiments, the NYCBOH strain of vaccinia virus can be ATCC VR-118 or CJ-MVB-SPX. ..

    Article Title: Cell-based vehicles for potentiation of viral therapy
    Article Snippet: .. In some embodiments, the NYCBOH strain of vaccinia virus can be ATCC VR-118 or CJ-MVB-SPX. ..

    Derivative Assay:

    Article Title: Live attenuated smallpox vaccine candidate (KVAC103) efficiently induces protective immune responses in mice.
    Article Snippet: .. The CJ-50300 smallpox vaccine used in this study was derived from American Type Culture Collection (ATCC) VR-118 (originating from the New York City Board of Health Vaccinia strain) and adapted for replication in MRC-5 cells under serum-free conditions without plaque purification [13]. ..

    Purification:

    Article Title: Live attenuated smallpox vaccine candidate (KVAC103) efficiently induces protective immune responses in mice.
    Article Snippet: .. The CJ-50300 smallpox vaccine used in this study was derived from American Type Culture Collection (ATCC) VR-118 (originating from the New York City Board of Health Vaccinia strain) and adapted for replication in MRC-5 cells under serum-free conditions without plaque purification [13]. ..



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    ATCC hantaan virus strain 76 118
    A) RLMVEC were infected with either SEOV or <t>HTNV</t> (MOI 0.05) or mock infected (-) and lysates were collected every 24 hours for six days (D1, D2, etc.) post-infection. Cell lysates were subjected to SDS-PAGE and immunoblot analysis for ISG expression. B) RLMVEC were infected with either SEOV or HTNV (MOI 0.05) and harvested 48 hours post-infection. Gene expression was assayed by comparative RT-PCR and averaged data from technical replicates and three experimental biological replicates are shown. Student’s T test, * denotes p<0.05. C) RLMVEC were infected with either HTNV or UV-inactivated HTNV or SEOV (MOI 0.05). Lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. D) RLMVEC were infected with either RLMVEC-passaged SEOV (RP SEOV) (MOI 0.025), UV-inactivated RLMVEC-passaged SEOV (UV RP SEOV) (0.025), or HTNV (MOI 0.025) and lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. Densitometry quantification of immunoblots in . All data shown are representative of ≥3 independent experiments.
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    ATCC reference number atcc vr118tm
    A) RLMVEC were infected with either SEOV or <t>HTNV</t> (MOI 0.05) or mock infected (-) and lysates were collected every 24 hours for six days (D1, D2, etc.) post-infection. Cell lysates were subjected to SDS-PAGE and immunoblot analysis for ISG expression. B) RLMVEC were infected with either SEOV or HTNV (MOI 0.05) and harvested 48 hours post-infection. Gene expression was assayed by comparative RT-PCR and averaged data from technical replicates and three experimental biological replicates are shown. Student’s T test, * denotes p<0.05. C) RLMVEC were infected with either HTNV or UV-inactivated HTNV or SEOV (MOI 0.05). Lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. D) RLMVEC were infected with either RLMVEC-passaged SEOV (RP SEOV) (MOI 0.025), UV-inactivated RLMVEC-passaged SEOV (UV RP SEOV) (0.025), or HTNV (MOI 0.025) and lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. Densitometry quantification of immunoblots in . All data shown are representative of ≥3 independent experiments.
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    ATCC vaccinia virus
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    ATCC atcc vr 118
    A) RLMVEC were infected with either SEOV or <t>HTNV</t> (MOI 0.05) or mock infected (-) and lysates were collected every 24 hours for six days (D1, D2, etc.) post-infection. Cell lysates were subjected to SDS-PAGE and immunoblot analysis for ISG expression. B) RLMVEC were infected with either SEOV or HTNV (MOI 0.05) and harvested 48 hours post-infection. Gene expression was assayed by comparative RT-PCR and averaged data from technical replicates and three experimental biological replicates are shown. Student’s T test, * denotes p<0.05. C) RLMVEC were infected with either HTNV or UV-inactivated HTNV or SEOV (MOI 0.05). Lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. D) RLMVEC were infected with either RLMVEC-passaged SEOV (RP SEOV) (MOI 0.025), UV-inactivated RLMVEC-passaged SEOV (UV RP SEOV) (0.025), or HTNV (MOI 0.025) and lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. Densitometry quantification of immunoblots in . All data shown are representative of ≥3 independent experiments.
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    Image Search Results


    A) RLMVEC were infected with either SEOV or HTNV (MOI 0.05) or mock infected (-) and lysates were collected every 24 hours for six days (D1, D2, etc.) post-infection. Cell lysates were subjected to SDS-PAGE and immunoblot analysis for ISG expression. B) RLMVEC were infected with either SEOV or HTNV (MOI 0.05) and harvested 48 hours post-infection. Gene expression was assayed by comparative RT-PCR and averaged data from technical replicates and three experimental biological replicates are shown. Student’s T test, * denotes p<0.05. C) RLMVEC were infected with either HTNV or UV-inactivated HTNV or SEOV (MOI 0.05). Lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. D) RLMVEC were infected with either RLMVEC-passaged SEOV (RP SEOV) (MOI 0.025), UV-inactivated RLMVEC-passaged SEOV (UV RP SEOV) (0.025), or HTNV (MOI 0.025) and lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. Densitometry quantification of immunoblots in . All data shown are representative of ≥3 independent experiments.

    Journal: PLOS Pathogens

    Article Title: Seoul orthohantavirus evades innate immune activation by reservoir endothelial cells

    doi: 10.1371/journal.ppat.1012728

    Figure Lengend Snippet: A) RLMVEC were infected with either SEOV or HTNV (MOI 0.05) or mock infected (-) and lysates were collected every 24 hours for six days (D1, D2, etc.) post-infection. Cell lysates were subjected to SDS-PAGE and immunoblot analysis for ISG expression. B) RLMVEC were infected with either SEOV or HTNV (MOI 0.05) and harvested 48 hours post-infection. Gene expression was assayed by comparative RT-PCR and averaged data from technical replicates and three experimental biological replicates are shown. Student’s T test, * denotes p<0.05. C) RLMVEC were infected with either HTNV or UV-inactivated HTNV or SEOV (MOI 0.05). Lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. D) RLMVEC were infected with either RLMVEC-passaged SEOV (RP SEOV) (MOI 0.025), UV-inactivated RLMVEC-passaged SEOV (UV RP SEOV) (0.025), or HTNV (MOI 0.025) and lysates were harvested at the indicated times post-infection and subjected to immunoblot analysis. Densitometry quantification of immunoblots in . All data shown are representative of ≥3 independent experiments.

    Article Snippet: Seoul virus strain SR11 and Hantaan virus strain 76–118 were propagated on Vero E6 cells (ATCC, CRL-1586) for 12 days.

    Techniques: Infection, SDS Page, Western Blot, Expressing, Gene Expression, Reverse Transcription Polymerase Chain Reaction

    A) RLMVECs were mock-infected or infected with SEOV (MOI 0.1) for 72 hours, followed by transfection with poly(I:C) (100 ng). RNA was collected 24-hours post-treatment to assess ISG expression. B-C) RLMVECs were mock-infected or infected with SEOV (MOI 0.1) for 48 hours (B) or 72 hours (C), followed by IFNβ treatment (100 U/mL). RNA was collected at 24 hours post-treatment to evaluate ISG induction. D) RLMVECs were mock-infected or infected with SEOV (MOI 0.05) for 5 days, followed by either mock infection or superinfection with SeV (150 HAU/mL). RNA was collected 24 hours after SeV infection to measure viral genome copies and ISG expression using qRT-PCR and comparative RT-PCR, respectively. E) RLMVEC Cas9 scramble, RIG-I -/- , or MDA5 -/- cells were either mock-infected or infected with SEOV (MOI 0.05) 48 hours. Cells were the either subsequently superinfected with HTNV (MOI 0.05) or mock-infected. Lysates were collected at the indicated times post-HTNV infection and subjected to SDS-PAGE and immunoblot analysis. Densitometry quantification of immunoblots in . All data shown represent ≥3 independent experiments, with technical replicates averaged within each experiment ±SD. One-way ANOVA with multiple comparisons to mock-infected poly(I:C), IFNβ, or SeV-treated control (* denotes p<0.05).

    Journal: PLOS Pathogens

    Article Title: Seoul orthohantavirus evades innate immune activation by reservoir endothelial cells

    doi: 10.1371/journal.ppat.1012728

    Figure Lengend Snippet: A) RLMVECs were mock-infected or infected with SEOV (MOI 0.1) for 72 hours, followed by transfection with poly(I:C) (100 ng). RNA was collected 24-hours post-treatment to assess ISG expression. B-C) RLMVECs were mock-infected or infected with SEOV (MOI 0.1) for 48 hours (B) or 72 hours (C), followed by IFNβ treatment (100 U/mL). RNA was collected at 24 hours post-treatment to evaluate ISG induction. D) RLMVECs were mock-infected or infected with SEOV (MOI 0.05) for 5 days, followed by either mock infection or superinfection with SeV (150 HAU/mL). RNA was collected 24 hours after SeV infection to measure viral genome copies and ISG expression using qRT-PCR and comparative RT-PCR, respectively. E) RLMVEC Cas9 scramble, RIG-I -/- , or MDA5 -/- cells were either mock-infected or infected with SEOV (MOI 0.05) 48 hours. Cells were the either subsequently superinfected with HTNV (MOI 0.05) or mock-infected. Lysates were collected at the indicated times post-HTNV infection and subjected to SDS-PAGE and immunoblot analysis. Densitometry quantification of immunoblots in . All data shown represent ≥3 independent experiments, with technical replicates averaged within each experiment ±SD. One-way ANOVA with multiple comparisons to mock-infected poly(I:C), IFNβ, or SeV-treated control (* denotes p<0.05).

    Article Snippet: Seoul virus strain SR11 and Hantaan virus strain 76–118 were propagated on Vero E6 cells (ATCC, CRL-1586) for 12 days.

    Techniques: Infection, Transfection, Expressing, Quantitative RT-PCR, Reverse Transcription Polymerase Chain Reaction, SDS Page, Western Blot, Control

    RLMVEC were either mock-infected or infected with SEOV (MOI 0.05) for 48 hours. Cells were subsequently either mock-infected or superinfected with HTNV (0.05 MOI) and fixed 48 hours post-HTNV infection. Images of immunostaining for SEOV nucleocapsid (green), MX1/2/3 (red), and DAPI (blue). Images were captured on an EVOS FL Auto imaging system using 20x magnification. Arrows indicate individual cells expressing both Mx1/2/3 and SEOV N. Images are representative of 2 independent experiments.

    Journal: PLOS Pathogens

    Article Title: Seoul orthohantavirus evades innate immune activation by reservoir endothelial cells

    doi: 10.1371/journal.ppat.1012728

    Figure Lengend Snippet: RLMVEC were either mock-infected or infected with SEOV (MOI 0.05) for 48 hours. Cells were subsequently either mock-infected or superinfected with HTNV (0.05 MOI) and fixed 48 hours post-HTNV infection. Images of immunostaining for SEOV nucleocapsid (green), MX1/2/3 (red), and DAPI (blue). Images were captured on an EVOS FL Auto imaging system using 20x magnification. Arrows indicate individual cells expressing both Mx1/2/3 and SEOV N. Images are representative of 2 independent experiments.

    Article Snippet: Seoul virus strain SR11 and Hantaan virus strain 76–118 were propagated on Vero E6 cells (ATCC, CRL-1586) for 12 days.

    Techniques: Infection, Immunostaining, Imaging, Expressing

    Primer sequences or catalog numbers for real-time PCR analyses.

    Journal: PLOS Pathogens

    Article Title: Seoul orthohantavirus evades innate immune activation by reservoir endothelial cells

    doi: 10.1371/journal.ppat.1012728

    Figure Lengend Snippet: Primer sequences or catalog numbers for real-time PCR analyses.

    Article Snippet: Seoul virus strain SR11 and Hantaan virus strain 76–118 were propagated on Vero E6 cells (ATCC, CRL-1586) for 12 days.

    Techniques: Real-time Polymerase Chain Reaction, Sequencing, Gene Expression