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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Search Our Publications
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Your search returned 2004 results.
|1996||Teaching About Science||Accountability in Research||Roberts, R.J.|
|1996||Potent Inhibition Of T7 Rna-Polymerase With A Truncated T7 Promoter.||Abstracts Of Papers Of The American Chemical Society||Noren, C.J., and Moreira, R.F.|
|2018||Platform development for expression and purification of stable isotope labeled monoclonal antibodies in Escherichia coli. mAbs||Abs||Reddy, P.T., Brinson, R.G., Hoopes, J.T., McClung, C., Ke, N., Kashi, L.|
|2010||Endosymbiont DNA in endobacteria-free filarial nematodes indicates ancient horizontal genetic transfer||5PLoS One||McNulty, S.N., Foster, J.M., Mitreva, M., Dunning-Hotopp, J.C., Martin, J., Fischer, K., Wu, B., Davis, P.J., Kumar, S., Brattig, N.W., Slatko, B.E., Weil, G.J. and Fischer, P.U.|
|2019||Staphylococcus aureus Cas9 is a multiple-turnover enzyme||Yourik, P|
|2001||Molecular Biology Problem Solver: A Laboratory Guide||Bonventre, J., Walsh, P.and Robinson, D.|
|2011||Next-gen expression systems||Ritter, A.|
|2011||Activity, specificity and structure of I-Bth03051: a representative of a new homing endonuclease family||Taylor, G.K., Heiter, D.F., Pietrokovski, S. and Stoddard, B.L.|
|2011||Branched Intermediate Formation is the Slowest Step in th Protein Splicing Reaction of the Ala1 KbA Intein from Methanococcus jannaschii||Saleh, L., Southworth, M.W., Considine, N., O'Neill, C., Benner, J., Bollinger, J.M. and Perler, F.B.|
|2011||6-Thioguanine reactivates epigenetically silenced genes in acute lymphoblastic leukemia cells by facilitating proteasome-mediated degradation of DNMT1||Canc. Res.|