Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jonglin TSAO"'
Autor:
Thomas B. Lavoie, Claudio Mapelli, Chester A. Meyers, Mariano Barbacid, Valentina Goldfarb, Bennett T. Farmer, Jonglin Tsao, Luciano Mueller, Michael Wittekind, Ki-Ling Suen
Publikováno v:
Biochemistry. 33:13531-13539
NMR spectroscopy has been used to characterize the protein-protein interactions between the mouse Grb2 (mGrb2) N-terminal SH3 domain complexed with a 15-residue peptide (SPLLPKLPP-KTYKRE) corresponding to residues 1264-1278 of the mouse Sos-2 (mSos-2
Autor:
Stephen M. Festin, Sesha Natarajan, Claudio Mapelli, S P Weinheimer, C.L. DiIanni, Jonglin Tsao, Douglas James Riexinger, Gregory Yamanaka, D A Drier, Mark S. Bolgar
Publikováno v:
Journal of Biological Chemistry. 268:25449-25454
Herpes simplex virus type-1 (HSV-1) protease is responsible for proteolytic processing of itself and the virus assembly protein ICP35 (infected cell protein 35). Two proteolytic processing sites within the protease have recently been identified betwe
Autor:
C. L. DiIanni, C. A. Meyers, Jonglin Tsao, Donald R. O'Boyle, D. A. Drier, J T Stevens, Claudio Mapelli, S P Weinheimer
Publikováno v:
Peptides 1994 ISBN: 9789072199218
Peptides 1994
Peptides 1994
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eadbc758c45a0ba904db13eafd0eece5
https://doi.org/10.1007/978-94-011-1468-4_359
https://doi.org/10.1007/978-94-011-1468-4_359
Publikováno v:
Analytical biochemistry. 197(1)
A method based on amino acid analysis has been developed for monitoring the covalent conjugation of synthetic peptide haptens to carrier proteins. The marker amino acid, alpha-aminobutyric acid, is included in the sequence during peptide synthesis. F
Autor:
STEVENS, John T., MAPELLI, Claudio, Jonglin TSAO, HAIL, Mark, O'BOYLE II, Donald, WEINHEIMER, Steven P., DIIANNI, Carolyn L.
Publikováno v:
European Journal of Biochemistry; 12/1/94, Vol. 226 Issue 2, p361-367, 7p, 3 Charts, 2 Graphs
Publikováno v:
Journal of Liquid Chromatography. 11:2005-2017
A procedure is described for the purification of synthetic methylphosphonate oligodeoxyribo-nucleosides. Syntheses were done on an automated instrument with the trityl group on in the last cycle. The oligomers were manually cleaved from the solid sup