We believe this site might serve you best:

United States

English Continue

This country code will remain if no action is taken to change it.

Don't see your country?
Promega Corporation
Home » Resources » Tools »

Citations Search

Catalog_banner_2014

Need Assistance? Chat

Sort By:

Proc. Natl. Acad. Sci. USA 101(7), 2112-2116. DNA-dependent PK inhibits adeno-associated virus DNA integration. 2004

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)

Expand Full Notes »

J. Biol. Chem. 274, 478-485. Nuclear extracts lacking DNA-dependent protein kinase are deficient in multiple round transcription. 1999

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)

Expand Full Notes »

Nature 394, 700-704. DNA-dependent protein kinase acts upstream of p53 in response to DNA damage. 1998

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)

Expand Full Notes »

J. Biol. Chem. 273, 1568-1573. Physical interaction between epidermal growth factor receptor and DNA-dependent protein kinase in mammalian cells. 1998

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)

Expand Full Notes »

J. Biol. Chem. 273, 25654-25658. Regulation of DNA-dependent protein kinase by the Lyn tyrosine kinase. 1998

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)

Expand Full Notes »

J. Biol. Chem. 273, 1794-1801. The XRCC4 gene product is a target for and interacts with the DNA-dependent protein kinase. 1998

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)

Expand Full Notes »

J. Biol. Chem. 272, 5647-5658. Sequence-specific DNA binding and transcription factor phosphorylation by Ku Autoantigen/DNA-dependent protein kinase. Phosphorylation of Ser- 527 of the rat glucocorticoid receptor. 1997

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)

Expand Full Notes »

J. Biol. Chem. 272, 23896-23904. Sites of UV-induced phosphorylation of the p34 subunit of replication protein A from HeLa cells 1997

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)

Expand Full Notes »

J. Biol. Chem. 272, 22191-22198. SV40 large tumor antigen nuclear import is regulated by the double- stranded DNA-dependent protein kinase site (Serine 120) flanking the nuclear localization sequence 1997

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)

Expand Full Notes »

It appears that you have Javascript disabled. Our website requires Javascript to function correctly. For the best browsing experience, please enable Javascript.

Scientists at Your Service

Scientists at Your Service

We offer a range of services to help you succeed using Promega technologies. From product training to set up of automated systems and development of custom applications—our scientific support goes beyond the basics.

Ask us! We are here to help you.