DNA Shearing Enzyme Mix for Next-Generation Sequencing Library Preparation
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DNA Shearing Enzyme Mix for Next-Generation Sequencing Library Preparation

Cat.No: ATR-SPS-0023 Datasheet

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Product Name DNA Shearing Enzyme Mix for Next-Generation Sequencing Library Preparation
Catalog No. ATR-SPS-0023
Description Dual-enzyme DNA fragmentation mix (endonuclease + nicking enzyme) for random, non-biased fragmentation to NGS-suitable sizes. Produces uniform fragment distributions without GC-content bias, requiring as little as 10 ng input DNA. Compatible with automation and generates 5'-phosphorylated, 3'-hydroxyl ends ready for library construction.
Intended Use Enzymatic DNA fragmentation for NGS; WGS, targeted panel, metagenomic, and ChIP-seq/ATAC-seq library preparation; PacBio/Oxford Nanopore library prep.
Principle / Technology DNA endonuclease introduces random double-strand breaks; nicking enzyme creates nicks converted to DSBs; balanced system eliminates sequence bias; incubation time controls fragment size (150-1,000 bp)
Detection Method Mix 10 ng-1 µg DNA with enzyme mix; incubate 5-25 min at 37 °C; inactivate 65 °C 10 min; proceed to end-repair
Sample Type Purified dsDNA; 10 ng-1 µg; A260/A280 1.8-2.0; free of EDTA, SDS, ethanol
Sensitivity / LOD Effective from 10 ng input; uniform fragments with CV <15%; tunable 150-1,000 bp
Specificity dsDNA specific; no detectable sequence/GC bias validated by NGS; RNA and ssDNA not substrates
Reaction Conditions / Protocol Fragmentation: 5-25 min at 37 °C; heat kill: 10 min 65 °C; total 20-40 min
Components / Formulation Fragmentation enzyme mix, reaction buffer (10×), inactivation solution, E. coli control DNA (100 ng/µL)
Storage Conditions -20 °C; avoid freeze-thaw; enzymes temperature-sensitive
Shelf Life 12 months at -20 °C; 3 months after first thaw
Package Specifications 25, 100, 500 reactions
Product Form Liquid enzyme mix in glycerol storage buffer
Key Features No sonication equipment needed; zero GC-bias; tunable size; 10 ng minimum input; automation compatible; ready ends for end-repair
Purity Recombinant, affinity-purified; no exonuclease/RNase/non-specific DNase; endotoxin <0.1 EU/µg
Concentration As specified on product label
Activity / Unit Definition Sample processing efficiency ≥90% recovery per validation protocol
Molecular Weight Not applicable or as specified for enzyme components
Source / Origin Synthetic and recombinant components as specified
pH Range / Optimal pH As stated in product specification
Shipping Conditions Cold pack -20 °C; do not thaw
Expiration Date / Stability 12 months at -20 °C; 3 months after thaw; aliquot first use; max 24 hr at 4 °C
Regulatory / Compliance For laboratory and research use only; RUO; ISO 9001
Compatibility Compatible with downstream PCR, mass spectrometry, and immunoassay workflows
Recommended Buffer System Use as directed; components optimized for stated application
Application Notes / Precautions Work quickly to prevent sample degradation; use appropriate protease/phosphatase inhibitors if needed
Batch-to-Batch Consistency Protein precipitation efficiency and analyte recovery within ±15% of reference lot

For research use only, not for clinical use.

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