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salt t4 dna ligase  (New England Biolabs)


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    Structured Review

    New England Biolabs salt t4 dna ligase
    Salt T4 Dna Ligase, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 98/100, based on 597 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/quick+ligase+buffer/NEBNext+Quick+Ligation+Reaction+Buffer/bio_rxiv__64898__2026__10__09__758087-286-19-24
    Average 98 stars, based on 597 article reviews
    salt t4 dna ligase - by Bioz Stars, 2026-11
    98/100 stars

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    Related Articles

    Ligation:

    Article Title: Single-cell measurement of higher-order 3D genome organization with scSPRITE
    Article Snippet: .. Next, each well was supplemented with 6.4 μl of ligation mix (220 μl of 2× Instant Sticky-end Ligase Master Mix (NEB, no. M0370), 352 μl of 5× Quick Ligase Buffer (NEB, no. B6058S) and 132 μl of 1,2-propanediol (Sigma-Aldrich, no. 398039)). .. The 96-well plate was sealed after loading a ligation mix and was mixed on an Eppendorf ThermoMixer C at 20 °C.

    Article Title: Adaptive sampling in nanopore sequencing for PCR-free random access in DNA data storage
    Article Snippet: .. For ligation, 10 μ L of Quick-Ligase Buffer (NEBNext Quick Ligation Module, NEB, UK) was mixed with 0.5 μ L of ATP (100 mM) and 1 μ L of T4 PNK (NEB, UK) with a 33.5 μ L normalized DNA solution (approx. ..

    Article Title: Compositions and methods for 3-hydroxypropionic acid production
    Article Snippet: The resulting 7695 bp vector fragment, from plasmid pGMEr121, and the resulting 1272 bp insert fragment comprising the AAT coding sequence, from plasmid pGMEr111, were separated by 0.8% agarose gel electrophoresis in 1×TBE buffer, excised from the gel, and purified using the QIAQUICK® Gel Extraction Kit (Qiagen) according to the manufacturer's instructions. .. A ligation reaction was then set up with 3 μL of vector fragment, 4 μL of insert fragment, 2 μL of sterile dd water, 10 μL of 2× Quick Ligase Buffer and 1 μL of Quick T4 Ligase (Quick Ligation Kit, New England Biolabs) and performed according to the manufacturer's instructions. .. A 5 μL aliquot of the ligation reaction above was transformed into XL10-Gold®Ultracompetent E. coli cells (Agilent Technologies) according to the manufacturer's instructions.

    Article Title: Single-cell measurement of higher-order 3D genome organization with scSPRITE
    Article Snippet: .. Each well was then supplemented with 6.4 μl of ligation mix (220 μl of 2× Instant Sticky-end Ligase Master Mix (NEB, no. M0370), 352 μl of 5× Quick Ligase Buffer (NEB, no. B6058S) and 132 μ of 1,2-propanediol (Sigma-Aldrich, no. 398039)). .. The 96-well plate was sealed after loading a ligation mix and was mixed on an Eppendorf ThermoMixer C at 20 °C.

    Article Title: Highly efficient chromatin conformation capture with post-enrichment in single cells by HiChew
    Article Snippet: .. For ligation, 220 μL of 2 × Instant Sticky-End Ligase Master Mix (New England Biolabs, Cat. No. M0370), 352 μL of 5 × Quick Ligase Buffer (New England Biolabs, Cat. No. B6058S), and 132 μL of 1,2-propanediol (Sigma-Aldrich, Cat. No. 398039) were mixed and 6.4 μL of mixture was distributed into each well of the plate containing the nuclei and adapters. ..

    Incubation:

    Article Title: Astrocyte-targeting therapy rescues cognitive impairment caused by neuroinflammation via the Nrf2 pathway
    Article Snippet: .. A-tailing reaction was performed using NEBNext dA-Tailing reaction buffer (NEB, 1×) with Klenow fragment exo(NEB, 7.5 U) at 37°C for 30 min. A-tailing reaction mixture was mixed with Quick Ligase Buffer (NEB), Quick ligase (NEB, 3,000 U), and 5 nM annealed adaptor (Illumina truncated adaptor) in a volume of 75 μL and incubated at 25°C for 20 min. .. The adaptor was prepared by annealing the following HPLC-purified oligos: 5′-phosphate/GATCGGAAGAGCACACGTCT-3′ and 5′- ACACTCTTTCCCTACACGACGCTCTTCCGATC∗T-3′ (∗phosphoro-thioate bond).

    Sterility:

    Article Title: Compositions and methods for 3-hydroxypropionic acid production
    Article Snippet: The resulting 7695 bp vector fragment, from plasmid pGMEr121, and the resulting 1272 bp insert fragment comprising the AAT coding sequence, from plasmid pGMEr111, were separated by 0.8% agarose gel electrophoresis in 1×TBE buffer, excised from the gel, and purified using the QIAQUICK® Gel Extraction Kit (Qiagen) according to the manufacturer's instructions. .. A ligation reaction was then set up with 3 μL of vector fragment, 4 μL of insert fragment, 2 μL of sterile dd water, 10 μL of 2× Quick Ligase Buffer and 1 μL of Quick T4 Ligase (Quick Ligation Kit, New England Biolabs) and performed according to the manufacturer's instructions. .. A 5 μL aliquot of the ligation reaction above was transformed into XL10-Gold®Ultracompetent E. coli cells (Agilent Technologies) according to the manufacturer's instructions.

    other:

    Article Title: Single-cell measurement of higher-order 3D genome organization with scSPRITE
    Article Snippet: Cells were washed with 1× PBS at a ratio of 4 ml of PBS per 1 × 10 7 cells and centrifuged again at 1,000 g for 4 min. After the wash, 4 ml of 1% formaldehyde (16% wt/vol formaldehyde ampules, Life Technologies, no. 28908, prepared in pre-warmed (37 °C) 1× PBS) was added per 1 × 10 7 cells to the conical tube, and the solution was mixed thoroughly by pipetting to remove clumps.



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