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quick dna rna pathogen miniprep kit  (Zymo Research)


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    Structured Review

    Zymo Research quick dna rna pathogen miniprep kit
    Quick Dna Rna Pathogen Miniprep Kit, supplied by Zymo Research, used in various techniques. Bioz Stars score: 94/100, based on 41 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/quick+dna+rna+pathogen+miniprep+kit/Quick-DNA%2FRNA+Pathogen+Miniprep/pmc13064018-22-11-15
    Average 94 stars, based on 41 article reviews
    quick dna rna pathogen miniprep kit - by Bioz Stars, 2026-10
    94/100 stars

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    Related Articles

    Clinical Proteomics:

    Article Title: Characterization of near-complete human Pegivirus 2 (HPgV-2) genomes in individuals co-infected with hepatitis C virus (HCV) in Cameroon
    Article Snippet: .. Then, 200 μL of plasma was extracted from each sample using Quick-DNA/RNA pathogen miniprep kit (Zymo Research, California, USA) and eluted in 50 μL of Dnase/Rnase-Free water, and viral genomes were sequenced using Sequence-Independent, Single-Primer Amplification (SISPA) ( ) method on the Oxford Nanopore platform (GridIon, R10.4.1 flow cells); purified nucleic acids were cleaned using RNA Clean XP beads (Beckman Coulter, California, USA) prior to complementary DNA (cDNA) synthesis with SuperScript IV Reverse Transcriptase (Thermo Fisher Scientific, USA). ..

    Sequencing:

    Article Title: Characterization of near-complete human Pegivirus 2 (HPgV-2) genomes in individuals co-infected with hepatitis C virus (HCV) in Cameroon
    Article Snippet: .. Then, 200 μL of plasma was extracted from each sample using Quick-DNA/RNA pathogen miniprep kit (Zymo Research, California, USA) and eluted in 50 μL of Dnase/Rnase-Free water, and viral genomes were sequenced using Sequence-Independent, Single-Primer Amplification (SISPA) ( ) method on the Oxford Nanopore platform (GridIon, R10.4.1 flow cells); purified nucleic acids were cleaned using RNA Clean XP beads (Beckman Coulter, California, USA) prior to complementary DNA (cDNA) synthesis with SuperScript IV Reverse Transcriptase (Thermo Fisher Scientific, USA). ..

    Amplification:

    Article Title: Characterization of near-complete human Pegivirus 2 (HPgV-2) genomes in individuals co-infected with hepatitis C virus (HCV) in Cameroon
    Article Snippet: .. Then, 200 μL of plasma was extracted from each sample using Quick-DNA/RNA pathogen miniprep kit (Zymo Research, California, USA) and eluted in 50 μL of Dnase/Rnase-Free water, and viral genomes were sequenced using Sequence-Independent, Single-Primer Amplification (SISPA) ( ) method on the Oxford Nanopore platform (GridIon, R10.4.1 flow cells); purified nucleic acids were cleaned using RNA Clean XP beads (Beckman Coulter, California, USA) prior to complementary DNA (cDNA) synthesis with SuperScript IV Reverse Transcriptase (Thermo Fisher Scientific, USA). ..

    Purification:

    Article Title: Characterization of near-complete human Pegivirus 2 (HPgV-2) genomes in individuals co-infected with hepatitis C virus (HCV) in Cameroon
    Article Snippet: .. Then, 200 μL of plasma was extracted from each sample using Quick-DNA/RNA pathogen miniprep kit (Zymo Research, California, USA) and eluted in 50 μL of Dnase/Rnase-Free water, and viral genomes were sequenced using Sequence-Independent, Single-Primer Amplification (SISPA) ( ) method on the Oxford Nanopore platform (GridIon, R10.4.1 flow cells); purified nucleic acids were cleaned using RNA Clean XP beads (Beckman Coulter, California, USA) prior to complementary DNA (cDNA) synthesis with SuperScript IV Reverse Transcriptase (Thermo Fisher Scientific, USA). ..

    cDNA Synthesis:

    Article Title: Characterization of near-complete human Pegivirus 2 (HPgV-2) genomes in individuals co-infected with hepatitis C virus (HCV) in Cameroon
    Article Snippet: .. Then, 200 μL of plasma was extracted from each sample using Quick-DNA/RNA pathogen miniprep kit (Zymo Research, California, USA) and eluted in 50 μL of Dnase/Rnase-Free water, and viral genomes were sequenced using Sequence-Independent, Single-Primer Amplification (SISPA) ( ) method on the Oxford Nanopore platform (GridIon, R10.4.1 flow cells); purified nucleic acids were cleaned using RNA Clean XP beads (Beckman Coulter, California, USA) prior to complementary DNA (cDNA) synthesis with SuperScript IV Reverse Transcriptase (Thermo Fisher Scientific, USA). ..

    Reverse Transcription:

    Article Title: Characterization of near-complete human Pegivirus 2 (HPgV-2) genomes in individuals co-infected with hepatitis C virus (HCV) in Cameroon
    Article Snippet: .. Then, 200 μL of plasma was extracted from each sample using Quick-DNA/RNA pathogen miniprep kit (Zymo Research, California, USA) and eluted in 50 μL of Dnase/Rnase-Free water, and viral genomes were sequenced using Sequence-Independent, Single-Primer Amplification (SISPA) ( ) method on the Oxford Nanopore platform (GridIon, R10.4.1 flow cells); purified nucleic acids were cleaned using RNA Clean XP beads (Beckman Coulter, California, USA) prior to complementary DNA (cDNA) synthesis with SuperScript IV Reverse Transcriptase (Thermo Fisher Scientific, USA). ..

    Homogenization:

    Article Title: Pan-Enterovirus Characterization Reveals Cryptic Circulation of Clinically Relevant Subtypes in Arizona Wastewater
    Article Snippet: Immediately following collection, samples were concentrated using the Environ Water RNA Kit (Zymo Research) following manufacturer protocol for viral enrichment and sample homogenization. .. Promptly after sample homogenization, samples were extracted using the Quick-DNA/RNA Pathogen Miniprep Kit (Zymo Research), including the optional Proteinase K treatment, following manufacturer protocol. ..

    RNA Sequencing:

    Article Title: Large-scale metagenomic surveillance study expands the known diversity of RNA viruses in mosquito populations from the Amazon Basin
    Article Snippet: .. Total nucleic acids were extracted from the mosquito pools using the Quick-DNA-RNA Pathogen Miniprep Kit (Zymo Research, Irvine, CA, USA). rRNA depletion and RNA sequencing library preparation were performed using the Illumina Stranded Total RNA Prep with Ribo-Zero Plus kit (Illumina, San Diego, CA, USA). .. The libraries were sequenced using two full flow cells of the Illumina NovaSeq 6000 platform at the University of Oregon’s Genomics and Cell Characterization Core Facility (GC3F).

    RNA Library Preparation:

    Article Title: Investigation of the causative pathogen in the 2023 conjunctivitis outbreak of Nepal using unbiased metagenomic next generation sequencing
    Article Snippet: .. At DHKUH, the swabs were extracted for DNA and RNA (Zymo Quick DNA/RNA Pathogen Miniprep Kit, Cat: R0142) followed by subsequent DNA and RNA library preparation (New England Biolabs) for metagenomic next generation sequencing. .. The respective libraries were pooled and quality checked by Agilent Tapestation and then loaded in Illumina iSeq100, with 4 million reads at 2x150 bp length.

    Next-Generation Sequencing:

    Article Title: Investigation of the causative pathogen in the 2023 conjunctivitis outbreak of Nepal using unbiased metagenomic next generation sequencing
    Article Snippet: .. At DHKUH, the swabs were extracted for DNA and RNA (Zymo Quick DNA/RNA Pathogen Miniprep Kit, Cat: R0142) followed by subsequent DNA and RNA library preparation (New England Biolabs) for metagenomic next generation sequencing. .. The respective libraries were pooled and quality checked by Agilent Tapestation and then loaded in Illumina iSeq100, with 4 million reads at 2x150 bp length.

    other:

    Article Title: Bat microfilariae in the cityscape: a transmission tale between bats, mites, and bat flies.
    Article Snippet: Molecular analyses were conducted using the same methodology; DNA was extracted from the blood samples of Litomosoidespositive individuals in smears fixed in DNA/RNA Shield (Zymo Research, USA), employing the Quick-DNA/RNA Pathogen Miniprep Kit (Zymo Research, USA).



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