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dna polymerase i  (New England Biolabs)


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    Structured Review

    New England Biolabs dna polymerase i
    Dna Polymerase I, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 10189 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/statistical+program+stata+version+12/DNA+Polymerase+I/us08557522-1051-33-36
    Average 99 stars, based on 10189 article reviews
    dna polymerase i - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Reverse Transcription:

    Article Title: Macrophage MERTK restrains GRAMD1A-driven mitochondrial oxysterol trafficking to limit colitis
    Article Snippet: Poly(A) RNA was purified from 1 μg total RNA using Dynabeads Oligo(dT) (Thermo Fisher) through two rounds of purification, followed by fragmentation with the Magnesium RNA Fragmentation Module (NEB) at 94 °C for 5-7 min. .. The fragmented RNA was reverse-transcribed into cDNA using SuperScriptTM II Reverse Transcriptase (Invitrogen) and subsequently used to synthesize U-labeled second-strand DNA with E. coli DNA polymerase I, RNase H (NEB), and dUTP solution (Thermo Fisher). ..

    Article Title: From disease model to therapeutic insight: An engineered hydrogel reveals the role of matrix viscous dissipation in intervertebral disc degeneration
    Article Snippet: .. The resulting RNA fragments were reverse-transcribed to create cDNA using SuperScriptTM Reverse Transcriptase (Invitrogen, USA), which was subsequently used to synthesize U-labeled second-stranded DNAs with E. coli DNA polymerase I (NEB, USA), RNase H (NEB, USA) and dUTP Solution (Thermo Fisher, USA). ..

    Article Title: Screening of M6a methylated genes associated with preovulatory follicle development in Bashang long-tailed chicken
    Article Snippet: The cleaved RNA fragments were incubated for 2 h at 4°C with m6A-specific antibody (No. 202003, Synaptic Systems, Germany) in IP buffer (50 mM Tris-HCl, 750 mM NaCl, and 0.5% Igepal CA-630). .. The immunoprecipitated RNA was reverse-transcribed to cDNA using SuperScript II Reverse Transcriptase (Invitrogen, cat. 1896649, USA), followed by synthesis of U-labeled second-stranded DNAs with E. coli DNA polymerase I (NEB, cat. m0209, USA), RNase H (NEB, cat. m0297, USA), and dUTP Solution (Thermo Fisher, cat. R0133, USA). ..

    cDNA Synthesis:

    Article Title: Integrated transcriptomic, proteomic, and metabolomic analyses reveal molecular mechanisms underlying clutch length differences in goose ovaries
    Article Snippet: The purified mRNA was then fragmented and reverse-transcribed into first-strand cDNA using SuperScript II Reverse Transcriptase (Thermo Fisher Scientific, MA, USA). .. Second-strand cDNA synthesis was performed incorporating dUTP (Thermo Fisher Scientific, MA, USA), DNA Polymerase I ( E. coli ) (New England Biolabs, MA, USA), and RNase H (New England Biolabs, MA, USA), to generate U-labeled double-stranded cDNA. .. Following end repair, 'A'-tailing, and adapter ligation, the U-labeled second strand was excised using Uracil-DNA Glycosylase (New England Biolabs, MA, USA).

    Article Title: Comparative effects of bile salts and free bile acids on intestinal health of grouper ( Epinephelus spp.) fed a high cottonseed protein concentrate diet
    Article Snippet: First-strand cDNA synthesis was conducted with random primers and Superscript II Reverse Transcriptase (catalog no. 18064014, Invitrogen, Carlsbad, CA, USA). .. Subsequently, second-strand cDNA synthesis was performed, employing DNA Polymerase I and RNase H provided in the NEBNext Ultra II Directional RNA Library Prep Kit for Illumina (catalog no. E7760S/L, New England Biolabs, Ipswich, MA, USA). ..

    Immunoprecipitation:

    Article Title: Screening of M6a methylated genes associated with preovulatory follicle development in Bashang long-tailed chicken
    Article Snippet: The cleaved RNA fragments were incubated for 2 h at 4°C with m6A-specific antibody (No. 202003, Synaptic Systems, Germany) in IP buffer (50 mM Tris-HCl, 750 mM NaCl, and 0.5% Igepal CA-630). .. The immunoprecipitated RNA was reverse-transcribed to cDNA using SuperScript II Reverse Transcriptase (Invitrogen, cat. 1896649, USA), followed by synthesis of U-labeled second-stranded DNAs with E. coli DNA polymerase I (NEB, cat. m0209, USA), RNase H (NEB, cat. m0297, USA), and dUTP Solution (Thermo Fisher, cat. R0133, USA). ..

    Polymerase Chain Reaction:

    Article Title: Engineering of the glucose uptake system to increase 2,4-Dihydroxybutyric acid production in Escherichia coli
    Article Snippet: The kits for plasmid DNA isolation and PCR clean-up were purchased from New England Biolabs (Frankfurt am Main, Germany) and used according to the instructions of the manufacturer. .. PCR reactions were performed with Q5 DNA polymerase (New England Biolabs) for all subcloning experiments. .. Dream Taq PCR Master Mix (ThermoFisher Scientific, Waltham, MA, USA) was used for colony PCR.

    Subcloning:

    Article Title: Engineering of the glucose uptake system to increase 2,4-Dihydroxybutyric acid production in Escherichia coli
    Article Snippet: The kits for plasmid DNA isolation and PCR clean-up were purchased from New England Biolabs (Frankfurt am Main, Germany) and used according to the instructions of the manufacturer. .. PCR reactions were performed with Q5 DNA polymerase (New England Biolabs) for all subcloning experiments. .. Dream Taq PCR Master Mix (ThermoFisher Scientific, Waltham, MA, USA) was used for colony PCR.



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