pcr buffer ii Search Results


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  • 90
    Thermo Fisher accuprime pcr buffer ii
    Accuprime Pcr Buffer Ii, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 445 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Thermo Fisher amplitaq gold pcr buffer ii
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    Thermo Fisher 10×accuprime pcr buffer ii
    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Thermo Fisher 1x pcr reaction buffer ii
    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Thermo Fisher 1×geneamp pcr buffer ii
    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Thermo Fisher 10×pcr buffer ii
    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Thermo Fisher 10ãƒâ— pcr buffer ii
    Inactivation of <t>MVA-VP2</t> by heat or UV irradiation . Agarose gel electrophoresis of <t>RT-PCR</t> product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.
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    Image Search Results


    Inactivation of MVA-VP2 by heat or UV irradiation . Agarose gel electrophoresis of RT-PCR product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.

    Journal: Antiviral Research

    Article Title: The immunogenicity of recombinant vaccines based on modified Vaccinia Ankara (MVA) viruses expressing African horse sickness virus VP2 antigens depends on the levels of expressed VP2 protein delivered to the host

    doi: 10.1016/j.antiviral.2018.04.015

    Figure Lengend Snippet: Inactivation of MVA-VP2 by heat or UV irradiation . Agarose gel electrophoresis of RT-PCR product of the AHSV-VP2 gene transcripts. DF-1 cells were infected with live, purified, heat or UV irradiated MVA-VP2 and 48 h later, VP2-mRNA detection was performed by RT-PCR.

    Article Snippet: Amplification of the VP2 gene was performed by PCR using PCR Buffer II (Invitrogen), dNTPs, specific primers (forward and reverse primers), MgCl2 solution, AmpliTaq DNA Polymerase (Invitrogen), and cDNA template.

    Techniques: Irradiation, Agarose Gel Electrophoresis, Reverse Transcription Polymerase Chain Reaction, Infection, Purification