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Song S., Lu Y., Choi Y.K., Han Y., Tang Q., Zhao G., Berns K.I. and Flotte T.R.
Notes: Using an in vitro model of recombinant adeno-associated virus (rAAV) integration, the authors examined if the presence or absence of DNA-Dependent Protein Kinase affected AAV integration. (3081)
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DNA-Dependent Protein Kinase
Woodard, R. L. , Anderson, M. G. , Dynan, W. S.
Notes: The SignaTECT® DNA-Dependent Protein Kinase Assay System was used to confirm the inhibitory effect of Wortmannin on the kinase activity of DNA-Dependent Protein Kinase (DNA-PK). (0152)
SignaTECT® DNA-Dependent Protein Kinase Assay System
Woo, R.A., McLure, K.G., Lees-Miller, S.P., Rancourt, D.E. and Lee, P.W.
Notes: Promega's SignaTECT® DNA-Dependent Protein Kinase Assay System was used in this study. (1962)
Bandyopadhyay, D., Mandal, M., Adam, L., Mendelsohn, J. and Kumar, R.
Notes: The authors used DNA-dependent Protein Kinase (DNA-PK) and substrate with several human carcinoma cell lines (1459)
Kumar, S., Pandey, P., Bharti, A., Jin, S., Weichselbaum, R., Weaver, D., Kufe, D., Kharbanda, S.
Notes: The authors used Promega's purified DNA-Dependent Protein Kinase as a substrate for in vitro phosphorylation by the protein tyrosine kinase Lyn. They also used the TNT® Coupled Reticulocyte Lysate System to synthesize radiolabeled DNA-dependent protein kinase (DNA-PK) catalytic subunit polypeptides for protein:protein interaction studies with GST-tagged Lyn. (0863)
TnT® SP6 Coupled Reticulocyte Lysate System
TnT® SP6 Coupled Reticulocyte Lysate System, Trial Size
TnT® T3 Coupled Reticulocyte Lysate System
TnT® T7 Coupled Reticulocyte Lysate System
TnT® T7 Coupled Reticulocyte Lysate System, Trial Size
TnT® T7/SP6 Coupled Reticulocyte Lysate System
TnT® T7/T3 Coupled Reticulocyte Lysate System
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Leber, R. , Wise, T. W. , Mizuta, R. , Meek, K.
Notes: The authors used Promega's DNA-dependent Protein Kinase (DNA-PK) and Recombinant Human AP1 for in vitro c-Jun kinase assays (0805)
Giffin, W., Kwast-Welfeld, J., Rodda, D.J., Prefontaine, G.G., Traykova-Andonova, M., Zhang, Y., Weigel, N.L., Lefebvre, Y.A., Hache, R.J.
Notes: The DNA-Dependent Protein Kinase (DNA-PK) was used to phosphorylate a GST-glucocorticoid receptor fusion protein. (1104)
Zernik-Kobak, M. , Vasunia, K. , Connelly, M. , Anderson, C. W. , Dixon, K.
Notes: DNA-Dependent Protein Kinase (DNA-PK) was used to in vitro phosphorylate replication protein A. The phosphorylation was compared to replication protein A isolated directly from HeLa cells. Many details of the reaction are provided. (0086)
Xiao, C. Y. , Hubner, S. , Jans, D. A.
Notes: Promega's Casein Kinase II and DNA-Dependent Protein Kinase were used for in vitro phosphorylation of the SV40 large T antigen expressed either from Rabbit Reticulocyte Lysate or a large Tantigen-β-Gal fusion protein expressed in a rat hepatoma cell line. Lysates and cell extracts were assayed for DNA-dependent protein kinase activity with a peptide substrate. The ability of β-Gal-T antigen fusions (± phosphorylation) to bind to murine importin subunits was assessed by an ELISA system using the Anti-β-Galactosidase mAb. (0120)
Anti-β-Galactosidase, Purified Monoclonal Antibody
DNA-Dependent Protein Kinase Peptide Substrate
Rabbit Reticulocyte Lysate System, Nuclease Treated
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