zymoclean large fragment dna recovery kit (Zymo Research)
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zymoclean large fragment dna recovery kit
Zymoclean Large Fragment Dna Recovery Kit, supplied by Zymo Research, used in various techniques. Bioz Stars score: 95/100, based on 201 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/zymoclean+large+fragment+dna+recovery+kit/Zymoclean+Large+Fragment+DNA+Recovery/bio_rxiv__64898__2026__02__24__707731-185-22-28
Average 95 stars, based on 201 article reviews
Zymoclean Large Fragment Dna Recovery Kit, supplied by Zymo Research, used in various techniques. Bioz Stars score: 95/100, based on 201 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/zymoclean+large+fragment+dna+recovery+kit/Zymoclean+Large+Fragment+DNA+Recovery/bio_rxiv__64898__2026__02__24__707731-185-22-28
Average 95 stars, based on 201 article reviews
zymoclean large fragment dna recovery kit - by Bioz Stars,
2026-11
95/100 stars
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Construct:Article Title: Phocaeicola dorei and Phocaeicola vulgatus Protect against Atherosclerosis by Regulating Gut Immunity Article Snippet: In addition, genomic DNAs were fragmented to an average size of 600 bp with the DNA Shearing System M220 (Covaris Inc., Woburn, MA, USA). .. Paired-end libraries were constructed with a TruSeq DNA PCR-Free Library Prep kit (Illumina, San Diego, CA, USA) and size-selected on agarose gels using a Polymerase Chain Reaction:Article Title: Phocaeicola dorei and Phocaeicola vulgatus Protect against Atherosclerosis by Regulating Gut Immunity Article Snippet: In addition, genomic DNAs were fragmented to an average size of 600 bp with the DNA Shearing System M220 (Covaris Inc., Woburn, MA, USA). .. Paired-end libraries were constructed with a TruSeq DNA PCR-Free Library Prep kit (Illumina, San Diego, CA, USA) and size-selected on agarose gels using a Article Title: Complete transition from chromosomal to cytoplasmic sex determination during prolonged Wolbachia symbiosis Article Snippet: Genomic DNA was also fragmented to an average size of 500 bp with the focused-ultrasonicator M220 (Covaris Inc., MA, USA). .. A paired-end library was prepared with the TruSeq DNA PCR-Free Library Prep Kit (Illumina, CA, USA) and size-selected using an agarose gel and the Agarose Gel Electrophoresis:Article Title: Complete transition from chromosomal to cytoplasmic sex determination during prolonged Wolbachia symbiosis Article Snippet: Genomic DNA was also fragmented to an average size of 500 bp with the focused-ultrasonicator M220 (Covaris Inc., MA, USA). .. A paired-end library was prepared with the TruSeq DNA PCR-Free Library Prep Kit (Illumina, CA, USA) and size-selected using an agarose gel and the Article Title: Regions of genome plasticity are systematically organized into recurrent integration spots that shape accessory-genome functional architecture: insights from a complete genome of strain F1C1 and pangenomic analysis of the Ralstonia solanacearum species complex Article Snippet: The tagmented sample was cleaned up using HighPrepTM PCR beads (Magbio, AC-60050) and subjected to strand displacement. .. The 3-5 kb size range of the strand displaced sample was selected using 0.6% agarose gel electrophoresis, followed by gel extraction using Article Title: Complete transition from chromosomal to cytoplasmic sex determination during prolonged Wolbachia symbiosis. Article Snippet: GenomicDNAwas also fragmented to an average size of 500 bpwith the focused-ultrasonicatorM220 (Covaris Inc., MA, USA). .. A paired-end library was prepared with the TruSeq DNA PCRFree Library Prep Kit (Illumina, CA, USA) and size-selected using an agarose gel and the Purification:Article Title: Novel insights into the genome organization of Rhizobiaceae : identification of linear plasmids. Article Snippet: .. Briefly, bands were cut out from the Eckhardt- type gels, and the DNA was purified using Gel Extraction:Article Title: Regions of genome plasticity are systematically organized into recurrent integration spots that shape accessory-genome functional architecture: insights from a complete genome of strain F1C1 and pangenomic analysis of the Ralstonia solanacearum species complex Article Snippet: The tagmented sample was cleaned up using HighPrepTM PCR beads (Magbio, AC-60050) and subjected to strand displacement. .. The 3-5 kb size range of the strand displaced sample was selected using 0.6% agarose gel electrophoresis, followed by gel extraction using Article Title: Assembly and cell-free expression of a partial genome for the synthetic cell Article Snippet: Gibson assembly of one or multiple linear fragments was performed in one of the following three ways. (i) Using the NEBuilder HiFi Master Mix (New England Biolabs) according to the manufacturer’s protocol, downscaled to 5 μL or 10 μL reaction volume and with an incubation of 1 h at 50 °C. (ii) Using the Gibson Assembly Master Mix (New England Biolabs) according to the manufacturer’s protocol. (iii) Using a protocol adapted from : A 5× ISO buffer (0.5M Tris-HCl pH 7.5, 50 mM MgCl 2 , 1 mM of each of the four dNTPs, 50 mM DTT, 25% PEG-8000, 5 mM NAD) was prepared according to the protocol in . .. Alternatively, Incubation:Article Title: Assembly and cell-free expression of a partial genome for the synthetic cell Article Snippet: Gibson assembly of one or multiple linear fragments was performed in one of the following three ways. (i) Using the NEBuilder HiFi Master Mix (New England Biolabs) according to the manufacturer’s protocol, downscaled to 5 μL or 10 μL reaction volume and with an incubation of 1 h at 50 °C. (ii) Using the Gibson Assembly Master Mix (New England Biolabs) according to the manufacturer’s protocol. (iii) Using a protocol adapted from : A 5× ISO buffer (0.5M Tris-HCl pH 7.5, 50 mM MgCl 2 , 1 mM of each of the four dNTPs, 50 mM DTT, 25% PEG-8000, 5 mM NAD) was prepared according to the protocol in . .. Alternatively, Centrifugation:Article Title: Assembly and cell-free expression of a partial genome for the synthetic cell Article Snippet: Gibson assembly of one or multiple linear fragments was performed in one of the following three ways. (i) Using the NEBuilder HiFi Master Mix (New England Biolabs) according to the manufacturer’s protocol, downscaled to 5 μL or 10 μL reaction volume and with an incubation of 1 h at 50 °C. (ii) Using the Gibson Assembly Master Mix (New England Biolabs) according to the manufacturer’s protocol. (iii) Using a protocol adapted from : A 5× ISO buffer (0.5M Tris-HCl pH 7.5, 50 mM MgCl 2 , 1 mM of each of the four dNTPs, 50 mM DTT, 25% PEG-8000, 5 mM NAD) was prepared according to the protocol in . .. Alternatively, other:Article Title: Giant genome of the vampire squid reveals the derived state of modern octopod karyotypes Article Snippet: Genomic DNA was extracted from the mantle tissue of Vampyroteuthis sp. and the ovary of A. hians using a Genomic-tip Kit (QIAGEN, Hilden, Germany) and was sheared into fragment sizes ranging from 15 kb to 20 kb with a g-tube device (Covaris Inc., MA, USA). |