CCL-34-VHG Search Results


  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
    • mdck stat1 ko cells  (ATCC)
    92
    ATCC mdck stat1 ko cells
    In vitro growth kinetics. ( A ) Alignment of the predicted IGIP in different mammalian species. The mature swine IGIP sequence used in this study is shown. ( B ) Schematic representation of the IGIP-H1 gene. The IGIP sequence and the components of the intergenic region are indicated. ( C ) Growth kinetics profiles of IGIP-H1att and H1att in MDCK and MDCK <t>STAT1</t> KO cells. Experiments were performed two times independently, each time in triplicate. Titers were determined by RT-qPCR and expressed as log 10 TCID50 equivalents. Gray area represents the area below the level of detection of the assay. ( D ) IGIP-H1att virus was serially passaged five times in MDCK (E1C5) cells and SPF eggs (E5), and the HA was amplified by RT-PCR, showing that the IGIP-H1 rearrangement is stable. Abbreviations: FP, fusion peptide; TM, transmembrane domain; CT, c-terminal region; G4S, poly-glycine protein linker; Furin CS, furin cleavage site; Tav2A, Thosea assigna virus 2A protein sequence; GlucS, Signal peptide of Gaussia luciferase.
    Mdck Stat1 Ko Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mdck stat1 ko cells/product/ATCC
    Average 92 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mdck stat1 ko cells - by Bioz Stars, 2023-03
    92/100 stars
    		  Buy from Supplier

    Image Search Results


    In vitro growth kinetics. ( A ) Alignment of the predicted IGIP in different mammalian species. The mature swine IGIP sequence used in this study is shown. ( B ) Schematic representation of the IGIP-H1 gene. The IGIP sequence and the components of the intergenic region are indicated. ( C ) Growth kinetics profiles of IGIP-H1att and H1att in MDCK and MDCK STAT1 KO cells. Experiments were performed two times independently, each time in triplicate. Titers were determined by RT-qPCR and expressed as log 10 TCID50 equivalents. Gray area represents the area below the level of detection of the assay. ( D ) IGIP-H1att virus was serially passaged five times in MDCK (E1C5) cells and SPF eggs (E5), and the HA was amplified by RT-PCR, showing that the IGIP-H1 rearrangement is stable. Abbreviations: FP, fusion peptide; TM, transmembrane domain; CT, c-terminal region; G4S, poly-glycine protein linker; Furin CS, furin cleavage site; Tav2A, Thosea assigna virus 2A protein sequence; GlucS, Signal peptide of Gaussia luciferase.

    Journal: Vaccines

    Article Title: Development of a Novel Live Attenuated Influenza A Virus Vaccine Encoding the IgA-Inducing Protein

    doi: 10.3390/vaccines9070703

    Figure Lengend Snippet: In vitro growth kinetics. ( A ) Alignment of the predicted IGIP in different mammalian species. The mature swine IGIP sequence used in this study is shown. ( B ) Schematic representation of the IGIP-H1 gene. The IGIP sequence and the components of the intergenic region are indicated. ( C ) Growth kinetics profiles of IGIP-H1att and H1att in MDCK and MDCK STAT1 KO cells. Experiments were performed two times independently, each time in triplicate. Titers were determined by RT-qPCR and expressed as log 10 TCID50 equivalents. Gray area represents the area below the level of detection of the assay. ( D ) IGIP-H1att virus was serially passaged five times in MDCK (E1C5) cells and SPF eggs (E5), and the HA was amplified by RT-PCR, showing that the IGIP-H1 rearrangement is stable. Abbreviations: FP, fusion peptide; TM, transmembrane domain; CT, c-terminal region; G4S, poly-glycine protein linker; Furin CS, furin cleavage site; Tav2A, Thosea assigna virus 2A protein sequence; GlucS, Signal peptide of Gaussia luciferase.

    Article Snippet: MDCK STAT1 KO cells (CCL-34-VHG) were purchased from ATCC.

    Techniques: In Vitro, Sequencing, Quantitative RT-PCR, Amplification, Reverse Transcription Polymerase Chain Reaction, Luciferase