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J. Biol. Chem. 281, 4754-4761. Casein Kinase II phosphorylation of the yeast phospholipid synthesis transcription factor Opi1p. 2006

Chang, Y-F. and Carman, G.M.

Notes: Opi1p is a transcriptional repressor that regulates phospholipid synthesis in yeast. Opi1p activity is regulated by protein kinase C (PKC) and cAMP-dependent protein kinase (PKA). This study investigates the role of casein kinase II (CaMK II) in regulation of Opi1p activity. PKC and PKA were used in phosphorylation studies to determine how specific mutations within Opi1p affect phosphorylation. (3536)

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J. Biol. Chem. 280, 26105-26112. Phosphorylation of the yeast choline kinase by protein kinase C. 2005

Choi, M-G., Kurnov, V., Kersting, M.C., Sreenivas, A., and Carman, G.M.

Notes: In this study, the authors investigated the role of Protein Kinase C in the phosphorylation of choline kinase, which is thought to play a role in the generation of human tumors. cAMP-Dependent Protein Kinase, Catalytic Subunit, and Protein Kinase C were used in phosphorylation reactions of pure choline kinase, immunoprecipitated choline kinase and choline kinase synthetic peptides. (3507)

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Eur. J. Biochem. 262, 95-101. Protein kinase C antagonizes pertussis-toxin-sensitive coupling of the calcitonin receptor to adenylyl cyclase. 1999

Shyu, J.-F., Zhang, Z., Hernandez-Lagunas, L., Camerino, C., Chen, Y., Inoue, D., Baron, R., Horne, W.C.

Notes: HEK cells expressing the C1a-calcintonin receptor were stimulated with either calcitonin or PMA following a 12-hour serum starvation. Cell lysates were prepared and assayed for protein kinase C activity with the SignaTECT® PKC Assay System. Excellent detail is provided for preparation of the cell lysates. (0402)

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Arterioscler. Thromb. Vasc. Biol. 19, 178-185. The proliferative effect of vascular endothelial growth factor requires protein kinase C-alpha and protein kinase C-zeta. 1999

Wellner, M., Maasch, C., Kupprion, C. , Lindschau, C., Luft, F. C., Haller, H.

Notes: The authors used the PepTag® Non-Radioactive PKC Assay with cultured human umbilical vein endothelial cells. (0178)

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Oncogene 16, 1643-1648. 9582011 1998

Yuan, Z.-M., Utsugisawa, T., Ishiko, T., Nakada, S., Huang, Y., Kharbanda, S., Weichselbaum, R., Kufe, D.

Notes: Recombinant GST-PKCdelta was incubated with either heat inactivated c-Abl and ATP or kinase-activated c-Abl and ATP. The GST-PKCdelta was then isolated with glutathione-sepharose beads and assayed with the PepTag® Non-Radioactive Protein Kinase Assay System. (0078)

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J. Immunol. 161, 4819-4824. The role of protein kinase C signaling in activated DRA transcription. 1998

Setterblad, N., Onyango, I., Pihlgren, U., Rask, L., Andersson, G.

Notes: The authors used the SignaTECT® Protein Kinase C (PKC) Assay System to measure activity of protein kinase C in soluble (cytosolic) and particulate (membrane) fractions of Raji B cells following stimulation with the phorbol ester TPA. (0424)

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EMBO J. 16, 2420-2430. A single serine residue at position 375 of VP16 is critical for complex assembly with Oct-1 and HCF and is a target of phosphorylation by casein kinase II. 1997

O'Reilly, D., Hanscombe, O., O'Hare, P.

Notes: The cAMP-dependent Protein Kinase (PKA) was used to in vitro phosphorylate VP16. Details are provided for the reaction buffers for each reaction. (0564)

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J. Biol. Chem. 272, 20063-20069. Adrenocorticotropin Induction of Stress-activated Protein Kinase in the Adrenal Cortex in vivo 1997

Watanabe, G., Pena, P., Albanese, C., Wilsbacher, L.D., Young, J.B. and Pestell, R.G.

Notes: The SignaTECT® Protein Kinase C (PKC) Assay System was used in this study. (2191)

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J. Clin. Invest. 100, 1180-1192. Stimulus coupling to transcription versus secretion in pheochromocytoma cells: Convergent and divergent signal transduction pathways and the crucial roles for route of cytosolic calcium entry and protein kinase C. 1997

Tang, K., Wu, Mahata, S.K., Mahata, M., Gill, B.M., Parmer, R.J. and O’Conner, D.T.

Notes: Kinase assays were performed on PC12 cell extracts. A lot of detail is given on preparation of cell extracts. Kinase activities were measured in the cytosol and membrane fractions. Kinase activities were determined in the presence or absence of 1mM nicotine. The SignaTECT® Protein Kinase C (PKC) and cAMP-Dependent (PKA) Protein Kinase Assay Systems were used in this study. (1532)

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J. Immunol. 154, 2092-2103. B cell superstimulatory influenza virus (H2-subtype) induces B cell proliferation by a PKC-activating, Ca2+-independent mechanism. 1995

Rott, O., Charreire, J., Semichon, M., Bismuth, G., Cash, E.

Notes: The PepTag® Non-Radioactive PKC Assay was used to monitor PKC levels in B lymphocyte cytoplasm and cell membranes. (0458)

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