Research
Phosphorylation of HIV-1 Tat by CDK2 in HIV-1 transcription
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* Corresponding author: Sergei Nekhai snekhai@howard.edu
1 Center for Sickle Cell Disease, Howard University College of Medicine, 520 W Street N.W., Washington, DC 20059, USA
2 Department of Biochemistry and Molecular Biology, Howard University College of Medicine, 520 W Street N.W., Washington, DC 20059, USA
3 Program in Genetics, Howard University College of Medicine, 520 W Street N.W., Washington, DC 20059, USA
4 Department of Biochemistry and Molecular Biology, The George Washington University Medical Center, 2300 I Street N.W., Washington, DC 20037, USA
5 Children's National Medical Center, CRI Center III, 111 Michigan Ave., N.W. Washington, D.C. 20010-2970, USA
Retrovirology 2006, 3:78 doi:10.1186/1742-4690-3-78
Published: 3 November 2006Additional files
Additional File 1:
Purification of CDK2/cyclin E. Mixed mono Q fractions of CDK2 and cyclin E (Mono Q lane) were purified on Superdex column. Fractions 37, 39, 41, 43, and 45 were analyzed for the presence of CDK2 and cyclin E by Coumassie staining.
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