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genomic sars cov 2 rna positive control  (ATCC)


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    Structured Review

    ATCC genomic sars cov 2 rna positive control
    Genomic Sars Cov 2 Rna Positive Control, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 87 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/control+strain/Quantitative+genomic+RNA+from+Severe+acute+respiratory+syndrome-related+coronavirus+2+strain+2019-nCoV%2FUSA-WA1%2F2020/pm42017669-155-5-14
    Average 95 stars, based on 87 article reviews
    genomic sars cov 2 rna positive control - by Bioz Stars, 2026-10
    95/100 stars

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    Amplification:

    Article Title: Nucleotide analogues
    Article Snippet: “Hydroxy” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound A. .. “Commercial Inhibitor” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the NSP12/RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs, in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and the commercial inhibitor. ..

    Article Title: Nucleotide analogues
    Article Snippet: “Phospho” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound C. “Fluoro” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound B. .. “Hydroxy” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound A. .. “Commercial Inhibitor” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the NSP12/RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs, in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and the commercial inhibitor.

    Article Title: Nucleotide analogues
    Article Snippet: “RNA Primer” This lane was loaded with specific RNA primers of approximately 24 bases, obtained from Eurofins Genomics. .. “RNA Control” This lane was loaded with genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC) “Positive Control” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs. .. “No-Adenosine” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs, in equimolar amounts, except that no rATP was included.

    Article Title: Nucleotide analogues
    Article Snippet: “RNA Control” This lane was loaded with genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC) “Positive Control” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs. .. “No-Adenosine” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs, in equimolar amounts, except that no rATP was included. .. “Phospho” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound C. “Fluoro” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound B.

    Article Title: Nucleotide analogues
    Article Snippet: “No-Adenosine” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs, in equimolar amounts, except that no rATP was included. .. “Phospho” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound C. “Fluoro” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound B. .. “Hydroxy” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs in equimolar amounts, except that the standard amount for rATP was split 50:50 between rATP and Compound A.

    Positive Control:


    Article Title: Nucleotide analogues
    Article Snippet: “RNA Primer” This lane was loaded with specific RNA primers of approximately 24 bases, obtained from Eurofins Genomics. .. “RNA
    Control” This lane was loaded with genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC) “Positive Control” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs. .. “No-Adenosine” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs, in equimolar amounts, except that no rATP was included.

    Article Title: Nationwide wastewater sequencing surveillance of SARS-CoV-2 lineages: validation against clinical data across 28 U.S. states
    Article Snippet: .. For all sequencing runs, SARS-CoV-2 gRNA (ATCC VR-1986D), an early isolate of the original SARS-CoV-2 virus from March of 2020 in Washington, is used as a positive control (GenBank: MT246667.1 ). ..

    Analogues:

    Article Title: Nucleotide analogues
    Article Snippet: .. The tested compounds were adenosine analogues: The RNA polymerase used in the assays consisted of the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix), SARS-CoV-2 genomic RNA (2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC)), and the primers used in the assays consisted of (RNA or DNA) complementary to specific region, from Eurofins. .. PCR reactions used the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and dNTPs/rNTPs, respectively.

    Control:

    Article Title: Nucleotide analogues
    Article Snippet: “RNA Primer” This lane was loaded with specific RNA primers of approximately 24 bases, obtained from Eurofins Genomics. .. “RNA Control” This lane was loaded with genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC) “Positive Control” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs. .. “No-Adenosine” This lane was loaded with the amplification product obtained from amplifying genomic RNA from the 2019 Novel Coronavirus; Strain: 2019-nCoV/USA-WA1/2020 (Reference: ATCC-VR-1986D, ATCC), using the RdRp catalytic domain of RNA-directed RNA polymerase (Reference: PX-COV-P006, ProteoGenix) of SARS-CoV2 and the RNA primers (same as the lane “RNA Primer”), using the 10× First Strand Buffer and RNase Inhibitor from Amino Allyl MessageAmpTM II aRNA Amplification Kit (Reference: AM1753, Thermo), and rNTPs, in equimolar amounts, except that no rATP was included.

    Sequencing:

    Article Title: Nationwide wastewater sequencing surveillance of SARS-CoV-2 lineages: validation against clinical data across 28 U.S. states
    Article Snippet: .. For all sequencing runs, SARS-CoV-2 gRNA (ATCC VR-1986D), an early isolate of the original SARS-CoV-2 virus from March of 2020 in Washington, is used as a positive control (GenBank: MT246667.1 ). ..

    Virus:

    Article Title: Nationwide wastewater sequencing surveillance of SARS-CoV-2 lineages: validation against clinical data across 28 U.S. states
    Article Snippet: .. For all sequencing runs, SARS-CoV-2 gRNA (ATCC VR-1986D), an early isolate of the original SARS-CoV-2 virus from March of 2020 in Washington, is used as a positive control (GenBank: MT246667.1 ). ..



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    86
    Jackson Laboratory tetracycline controlled transactivator protein rtta m2 jackson labs strain 031285
    EC 50 results for Vibrio strains against GATR-3, LL-37-NH 2 , and Mastoparan-AF-NH 2 peptides. Vibrio vulnificus MO6 EC 50 results against A. GATR-3, B. LL-37-NH 2 , and C. Mastoparan-AF-NH 2 peptides. Vibrio vulnificus JY1701 EC 50 results against D. GATR-3, E. LL-37-NH 2 , and F. Mastoparan-AF-NH 2 peptides. Vibrio parahaemolyticus NY477 EC 50 results against G. GATR-3, H. LL-37-NH 2 , and I. Mastoparan-AF-NH 2 peptides. Vibrio parahaemolyticus SAK11 EC 50 results against J. GATR-3, K. LL-37-NH 2 , and L. Mastoparan-AF-NH 2 peptides. <t>Escherichia</t> <t>coli</t> EC 50 results against M. GATR-3, N. LL-37-NH 2 , and O. Mastoparan-AF-NH 2 peptides.
    Tetracycline Controlled Transactivator Protein Rtta M2 Jackson Labs Strain 031285, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    EC 50 results for Vibrio strains against GATR-3, LL-37-NH 2 , and Mastoparan-AF-NH 2 peptides. Vibrio vulnificus MO6 EC 50 results against A. GATR-3, B. LL-37-NH 2 , and C. Mastoparan-AF-NH 2 peptides. Vibrio vulnificus JY1701 EC 50 results against D. GATR-3, E. LL-37-NH 2 , and F. Mastoparan-AF-NH 2 peptides. Vibrio parahaemolyticus NY477 EC 50 results against G. GATR-3, H. LL-37-NH 2 , and I. Mastoparan-AF-NH 2 peptides. Vibrio parahaemolyticus SAK11 EC 50 results against J. GATR-3, K. LL-37-NH 2 , and L. Mastoparan-AF-NH 2 peptides. Escherichia coli EC 50 results against M. GATR-3, N. LL-37-NH 2 , and O. Mastoparan-AF-NH 2 peptides.

    Journal: Comparative Immunology Reports

    Article Title: The synthetic peptide GATR-3 shows significant antibacterial and biofilm-inhibition activity against shellfish- and oyster-associated bacteria Vibrio vulnificus and Vibrio parahaemolyticus

    doi: 10.1016/j.cirep.2025.200266

    Figure Lengend Snippet: EC 50 results for Vibrio strains against GATR-3, LL-37-NH 2 , and Mastoparan-AF-NH 2 peptides. Vibrio vulnificus MO6 EC 50 results against A. GATR-3, B. LL-37-NH 2 , and C. Mastoparan-AF-NH 2 peptides. Vibrio vulnificus JY1701 EC 50 results against D. GATR-3, E. LL-37-NH 2 , and F. Mastoparan-AF-NH 2 peptides. Vibrio parahaemolyticus NY477 EC 50 results against G. GATR-3, H. LL-37-NH 2 , and I. Mastoparan-AF-NH 2 peptides. Vibrio parahaemolyticus SAK11 EC 50 results against J. GATR-3, K. LL-37-NH 2 , and L. Mastoparan-AF-NH 2 peptides. Escherichia coli EC 50 results against M. GATR-3, N. LL-37-NH 2 , and O. Mastoparan-AF-NH 2 peptides.

    Article Snippet: Against the control strain E. coli ATCC 25922, GATR-3 was extremely potent, with an EC50 of 4.44 × 10−5 μM (1.27 × 10−4 μg/mL), confirming its broad-spectrum and potent efficacy.

    Techniques:

    Biofilm Formation of Vibrio isolates and E. coli . Quantitative comparison of biofilm formation among Vibrio isolates and E. coli after 24 h incubation. Biofilm biomass was determined by crystal violet staining and measurement of OD₆₀₀. V. vulnificus MO6 and V. parahaemolyticus NY477 exhibited the highest biofilm-forming capacities.

    Journal: Comparative Immunology Reports

    Article Title: The synthetic peptide GATR-3 shows significant antibacterial and biofilm-inhibition activity against shellfish- and oyster-associated bacteria Vibrio vulnificus and Vibrio parahaemolyticus

    doi: 10.1016/j.cirep.2025.200266

    Figure Lengend Snippet: Biofilm Formation of Vibrio isolates and E. coli . Quantitative comparison of biofilm formation among Vibrio isolates and E. coli after 24 h incubation. Biofilm biomass was determined by crystal violet staining and measurement of OD₆₀₀. V. vulnificus MO6 and V. parahaemolyticus NY477 exhibited the highest biofilm-forming capacities.

    Article Snippet: Against the control strain E. coli ATCC 25922, GATR-3 was extremely potent, with an EC50 of 4.44 × 10−5 μM (1.27 × 10−4 μg/mL), confirming its broad-spectrum and potent efficacy.

    Techniques: Comparison, Incubation, Staining