We believe that basic research and the cultivation of scientific knowledge is critical for us to stay connected with our customers and to drive scientific breakthroughs. At NEB, over 30 labs participate in research projects, which are aided by post-doctoral fellows and students in Masters and Ph.D. programs. NEB researchers have authored or co-authored over 1,200 publications (as of 1/19) many of which are in peer-reviewed journals. Further, NEB products have been used successfully in numerous publications by scientists throughout the world.
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Your search returned 2075 results.
|2015||The use of museum specimens with high-throughput DNA sequen.||J Hum Evol.||Burrell AS, Disotell TR, Bergey CM.|
|2008||The way forward, enhanced characterization of therapeutic antibody glycosylation: comparison of three level mass spectrometry-based strategies||J. Chromatogr. B Analyt. Technol. Biomed. Life Sci.||Wagner-Rousset, E., Bednarczyk, A., Bussat, M.C., Colas, O., Corvaïa, N., Schaeffer, C., Van Dorsselaer, A., Beck, A.||Glycobiology and Proteomics|
|2019||The yeast scavenger decapping enzyme DcpS and its application for in vitro RNA recapping||Sci Rep||Wulf MG, Buswell J, Chan SH, Dai N, Marks K, Martin ER, Tzertzinis G, Whipple JM, Corrêa IR Jr, Schildkraut I.|
|2019||The yeast scavenger decapping enzyme DcpS and its application for in vitro RNA recapping||Sci Rep||Wulf, M.G.|
|2014||Therapeutic epitopes of Leptospira LipL32 protein and their characteristics||Protein Eng Des Sel||Maneewatch S, Adisakwattana P, Chaisri U, Saengjaruk P, Srimanote P, Thanongsaksrikul J, Sakolvaree Y, Poungpan P, Chaicumpa W||Phage Display|
|1999||Thermal Asymmetric Interlaced PCR Amplification of YAC Insert End Fragments for Chromosome Walking in Plasmodium falciparum and Other A/T-Rich Genomes.||BioTechniques||Foster, J.M., Christodoulou, Z., Cowan, G.M.and Newbold, C.I.|
|1994||Thermal cycle Dideoxy DNA Sequencing.||Methods Mol.Biol.||Slatko, B.E.|
|1996||Thermal cycle dideoxy DNA sequencing||Methods Mol.Biol.||Slatko, B.|
|2019||Therminator DNA polymerase: Modified nucleotides and unnatural substrates||Front Mol Biosci||Gardner, A.F., Jackson, K.M., Boyle, M.M., Buss, J.A., Potapov, V., Gehring, A.M., Zatopek, K.M., Correa, I.R., Jr., Ong, J.L., Jack. W.E.||DNA Amplification PCR and qPCR|
|1996||Thermostable Bst DNA polymerase I lacks a 3' fwdarw 5' proofreading exonuclease activity1.||Genetic Analysis Biomolecular Engineering||Aliotta, J.M., Pelletier, J.J., Ware, J.L., Moran, L.S., Benner, J.S., and Kong, H.|