- Protein Expression|Protein Purification|Protein Tools
- DNA Modifying Enzymes and Cloning Technologies|Next Generation Sequencing Library Preparat
- DNA修饰酶
- DNA Assembly Cloning and Mutagenesis Kits
- DNA修饰酶和克隆技术|NGS样品制备&;目标富集|PCR
- 缓冲液|下一代测序文库制备|NGS样品制备&;目标富集
- Protein Expression|Protein Expression & Purification Technologies|Protein Purification
- 表观遗传学|限制性内切酶
- DNA Modifying Enzymes and Cloning Technologies|Epigenetics
- Nucleic Acid Purification|RNA Reagents
- 表观遗传学
- DNA Modifying Enzymes and Cloning Technologies
- Buffers|DNA Modifying Enzymes and Cloning Technologies|PCR, Polymerases & Amplificatio
- Buffers|Markers & Ladders|RNA Reagents
- Next Generation Sequencing Library Preparation|NGS Sample Prep & Target Enrichment
- Nucleic Acid Purification|Protein Expression & Purification Technologies|RNA Reagents
- Next Generation Sequencing Library Preparation|PCR, Polymerases & Amplification Techno
- Buffers|DNA Modifying Enzymes and Cloning Technologies
- Buffers|Competent Cells
- DNA Modifying Enzymes and Cloning Technologies|Next Generation Sequencing Library Preparat
- Next Generation Sequencing Library Preparation|PCR, Polymerases & Amplification Techno
NEBNext® dsDNA Fragmentase generates dsDNA breaks in a time-dependent manner to yield 50–1,000 bp DNA fragments depending on reaction time. NEBNext dsDNA Fragmentase contains two enzymes, one randomly generates nicks on dsDNA and the other recognizes the nicked site and cuts the opposite DNA strand across from the nick, thereby producing dsDNA breaks. The resulting DNA fragments contain short overhangs, 5´-phosphates, and 3´-hydroxyl groups. The random nicking activity of NEBNext dsDNA Fragmentase has been confirmed by preparation of libraries for next-generation sequencing. A comparison of the sequencing results between libraries prepared with genomic DNA sheared with NEBNext dsDNA Fragmentase and with mechanical shearing demonstrates that NEBNext dsDNA Fragmentase does not introduce any detectable bias during sequencing library preparation and no difference in sequence coverage is observed between the two methods.For larger volume requirements, customized and bulk packaging is available by purchasing through the OEM/Bulks department at NEB. Please contact custom@neb.com for further information.
Reaction Definition: One reaction is defined as the amount of NEBNext dsDNA Fragmentase required to convert 1 µg of purified HeLa cell gDNA in 20 µl of 1X NEBNext dsDNA Fragmentase Reaction Buffer v2 into short (100–300 bp) DNA fragments in 30 minutes at 37°C.
- This product is related to the following categories:
- DNA Fragmentation & RNA Fragmentation