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 2024 results.
|2007||Fusion of Gaussia luciferase to an engineered anti-carcinoembryonic antigen (CEA) antibody for in vivo optical imaging||Mol. Imaging Biol.||Venisnik, K.M., Olafsen, T., Gambhir, S.S., Wu, A.M.|
|2001||The sequence of the human genome||Science||Venter, J.C., Roberts, R.J.et al.|
|2002||Recombinant Gaussia luciferase. Overexpression, purification, and analytical application of a bioluminescent reporter for DNA hybridization||Anal Chem.||Verhaegen, M. and Christopoulos, T.K.|
|2002||Recombinant Gaussia luciferase. Overexpression, purification and analytical application of a bioluminescent reporter for DNA hybridization||Anal Chem||Verhaegen, M., Christopoulos, T.K.|
|2011||Screening of genetic parameters for soluble protein expression in Escherichia coli||Protein Expression and Purification||Vernet, E., Kotzsch, A., Voldborg, B., et al.|
|2000||Crystallization of Restriction Endonuclease BamHI with Nonspecific DNA.||J.Struct.Biol.||Viadiu, H., Kucera, R., Schildkraut, I.and Aggarwal, A.K.|
|2003||Crystallization of restriction endonuclease SfiI in complex with DNA||Acta Crystallogr. D Biol. Crystallogr.||Viadiu, H., Vanamee, E.S., Jacobson, E.M., Schildkraut, I. and Aggarawl, A.K.|
|2014||Procerain B, a cysteine protease from Calotropis procera, requires N-terminus pro-region for activity: cDNA cloning and expression with pro-sequence.||Protein Expr Purif||Vidhyadhar Nandana, Sushant Singh, Abhay Narayan Singh, Vikash Kumar Dubey||High-Fidelity PCR|
|2006||Highly efficient ribosome display selection by use of purified components for in vitro translation||J. Immunol Methods||Villemagne, D., Jackson, R. and Douthwaite, J.A.|
|2010||USER friendly DNA recombination (USERec): a simple and flexible near homology-independent method for gene library construction||Protein Eng Des Sel||Villiers BR, Stein V, Hollfelder F||USER™ Cloning|