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- α1-3,6 Galactosidase Application Note
- β-N-Acetylglucosaminidase Application Note
- 2017-18 Catalog Feedback
- 2017-18 NEB Catalog Request Form
- A Fast One-Step Digestion of DNA or RNA for Global Detection and Characterization of Nucleotide Modifications
- A Modern Day Gene Genie Sir Richard Roberts on Rebase
- About NEB
- About PNGase F
- ABRF 2014
- Acids and Bases
- ACP-tag and MCP-tag
- Activity at 37°C for Restriction Enzymes with Alternate Incubation Temperatures
- Activity of DNA Modifying Enzymes in CutSmart® Buffer
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- Adaptors and Primers for Library Prep
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- Additional E. coli Strain Genotypes
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- Affinity Isolation and Purification Matricies
- Affinity of Protein A/G for IgG Types from Different Species
- Agarose Gel Resolution
- AGBT 2018 Wellcome Sanger Institute poster: Thurston. S., et al. (2018). A Large Genome Centre Core Pipeline Refresh.
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- Alphabetized List of Recognition Specificities
- Alteration of Apparent Recognition Specificities Using Methylases
- Amino Acid Structures
- Analysis of 5-methylcytosine and 5-hydroxymethylcytosine Levels in Human Brain and Liver DNA Samples using the EpiMark® 5-hmC and 5-mC Analysis Kit
- Analysis of a Fusion Protein using the Protein Deglycosylation Mix II and Mass Spectrometry
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- Co-expression of Multiple Proteins in Kluyveromyces lactis N3742
- Co-expression of Multiple Proteins in Kluyveromyces lactis N3743
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- Detailed characterization of antibody glycan structure using exoglycosidases
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- Efficient Adaptor Ligation for the Preparation of dsDNA Libraries using the Blunt/TA Ligase Master Mix
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- Enhance your DNA purification experience
- Enhancing Transformation Efficiency C2523
- Enhancing Transformation Efficiency C2925
- Enhancing Transformation Efficiency C2984
- Enhancing Transformation Efficiency C2987
- Enhancing Transformation Efficiency C2988
- Enhancing Transformation Efficiency C2992
- Enhancing Transformation Efficiency C3019
- Enhancing Transformation Efficiency C3037
- Environmental Commitment
- Enzymatic PCR cleanup using Exonuclease I and Shrimp Alkaline Phosphatase
- Enzymatic PCR cleanup using Exonuclease I and Shrimp Alkaline Phosphatase
- Enzymatic removal of N- and O-glycans using PNGase F or the Protein Deglycosylation Mix
- Enzymatic removal of N- and O-glycans using PNGase F or the Protein Deglycosylation Mix P0705
- Enzymatic removal of N- and O-glycans using PNGase F or the Protein Deglycosylation Mix P6039
- Enzyme Finder
- Enzyme Finder
- Enzyme Finder - Sequence > 6 Bases
- Enzymes For Innovation
- Enzymes with Multiple Recognition Sequences
- Enzymes with Nonpalindromic Sequences
- Epigenetic Analysis
- Epigenetic Analysis (Epimark® Validated)
- Epigenetic Analysis (EpiMark® Validated) Products
- Epigenetics - Expanding on Genomic Foundations
- Epigenetics Brochure
- Epigenetics Products
- Epigenetics Products
- EpiMark® Methylated DNA Enrichment Kit Troubleshooting Guide
- Everything You Ever Wanted to Know About Type II Restriction Enzymes
- Exoglycosidases
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- First successful PCR experiment performed in space
- Five Steps to a Greener Lab: A roadmap to environmental action
- Flexible Preparation of High Quality NGS DNA Libraries with the NEBNext Ultra II DNA Library Prep Kit on the Tecan® Freedom Evo® NGS Workstation
- Fluorescent Labeling of COS-7 Expressing SNAP-tag® Fusion Proteins for Live Cell Imaging
- For What Applications is Fidelity Important?
- For What Applications is Fidelity Important?
- Foundations of Molecular Cloning - Past, Present and Future
- Freezer Details
- Freezer Program
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- Frequencies of Restriction Sites
- Gaussia and Cypridina Luciferases - Ultrasensitive secreted reporters and their use in dual assays
- Gaussia Luciferase
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- Georgetown University
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- Getting Started with Molecular Cloning: Simple Tips to Improve your Cloning Efficiency
- Getting Started with RNA-Sequencing (RNA-Seq)
- Gibson Assembly® - Building a Synthetic Biology Toolset
- Ginkgo Bioworks NEBnow
- Global Conservation
- Glycan Analysis of Murine IgG by Enzymatic Digestion
- Glycan Analysis of Murine IgG2a by Enzymatic Digestion with PNGase F and Trypsin, Followed by Mass Spectrometric Analysis
- Glycobiology
- Glycobiology Brochure
- Glycobiology Buffers & Diluents
- Glycobiology Products
- Glycobiology Unit Conversion Chart
- Glycomics: A rapidly evolving field with a sweet future
- Glycoprotein Substrates
- Glycoproteomics Brochure
- Glycoproteomics Technical Guide
- Glycosidases Double Digest Chart
- GRCh37hg19 BED files for the NEBNext Direct Cancer HotSpot Panel
- GRCh37hg19 Bed Files for the NEBNext Direct® BRCA1/BRCA2 Panel
- GRCh38/hg38 BED files for the NEBNext Direct® Cancer HotSpot Panel
- GRCh38hg38 Bed Files for the NEBNext Direct® BRCA1/BRCA2 Panel
- Greater Confidence in Result Accuracy
- Guidance on Choosing Sample Input Amounts when Using the Monarch Total RNA Miniprep Kit
- Guidelines for PCR Optimization with OneTaq® and OneTaq® Hot Start DNA Polymerases
- Guidelines for PCR Optimization with Taq DNA Polymerase
- Guidelines for PCR Optimization with Thermophilic DNA Polymerases
- Guidelines for Purification of RNA from Cultured Mammalian Cells
- Guidelines for RNA Purification from Bacteria
- Guidelines for RNA Purification from Leukocytes (WBCs, PBMCs)
- Guidelines for RNA Purification from Plants
- Guidelines for RNA Purification from Tissues
- Guidelines for RNA Purification from Whole Blood
- Guidelines for RNA Purification from Yeast
- Guidelines for RNA Quantitation
- Guidelines for Sample Stabilization Using the Monarch DNA/RNA Protection Reagent
- Guidelines for Working with RNA During RNA Cleanup
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- Highly-pure DNA for downstream applications
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- How Does a High-Fidelity Polymerase Ensure that the Correct Base is Inserted?
- How Does a High-Fidelity Polymerase Ensure that the Correct Base is Inserted?
- How is Fidelity Measured?
- How is Fidelity Measured?
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- Improved Library Preparation with NEBNext Ultra II DNA Library Prep Kit for Illumina
- Improved method for assembly of linear yeast expression cassette using NEBuilder® HiFi DNA Assembly Master Mix
- Improved methods for site-directed mutagenesis using Gibson Assembly Master Mix
- Improved methods for site-directed mutagenesis using Gibson Assembly™ Master Mix
- Improved methods for site-directed mutagenesis using NEBuilder® HiFi DNA Assembly Master Mix
- Improvements in Library Quality
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- Improving Enzymatic DNA Fragmentation for Next Generation Sequencing Library Construction
- Indiana University
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- Intein-Mediated Protein Ligation (IPL) and Labeling with the IMPACT™ Kit
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6702
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6703
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6704
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6706
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6707
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6709
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6710
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6906
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6951
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6952
- Intein-Mediated Protein Ligation IPL and Labeling with the IMPACT Kit N6953
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