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- 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
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Description:
NEBextensivelyperformsqualitycontrolsonallstandardandhigh-fidelity(HF®)restrictionenzymes.ExamplesofnucleasecontaminationstudiesforsomeofourHFrestrictionenzymesareshownbelow.
RestrictionEnzymeCompetitorStudy:NucleaseContamination
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EcoRI,NotI,andBamHIfrommultiplesuppliersweretestedinreactionscontainingafluorescentlabeledsinglestranded,doublestrandedblunt,3’overhangor5’overhangcontainingoligonucleotides.Thepercentdegradationisdeterminedbycapillaryelectrophoresisandpeakanalysis.Theresolutionisatthesinglenucleotidelevel.
ProductSource
AnE.colistrainthatcarriestheclonedandmodifiedBsrGIgenefromBacillusstearoThermophilusGR75(Z.Chen)ReagentsSupplied
Thefollowingreagentsaresuppliedwiththisproduct:
Storeat(°C) | Concentration | |
CutSmart®Buffer | -20 | 10X |