Characterization of the VIP receptor from SUP T1 lymphoblasts

1996 ◽  
Vol 6 (1) ◽  
pp. 49-57 ◽  
Author(s):  
Patrick Robberecht ◽  
Philippe Gourlet ◽  
Pascale Vertongen ◽  
Michal Svoboda
Keyword(s):  
1994 ◽  
Vol 205 (3) ◽  
pp. 1617-1624 ◽  
Author(s):  
M. Svoboda ◽  
M. Tastenoy ◽  
J. Vanrampelbergh ◽  
J.F. Goossens ◽  
P. Deneef ◽  
...  

1989 ◽  
Vol 26 (2) ◽  
pp. 117-126 ◽  
Author(s):  
Patrick Robberecht ◽  
Philippe De Neef ◽  
Philippe Gourlet ◽  
Annick Cauvin ◽  
David H. Coy ◽  
...  

FEBS Letters ◽  
1992 ◽  
Vol 300 (2) ◽  
pp. 149-152 ◽  
Author(s):  
Jonathan S. Cook ◽  
Dana Hance Wolsing ◽  
Jelveh Lameh ◽  
Christy A. Olson ◽  
Paul E. Correa ◽  
...  

1997 ◽  
Vol 321 (3) ◽  
pp. 379-386 ◽  
Author(s):  
David Pozo ◽  
Manuel L Montilla ◽  
Juan M Guerrero ◽  
Juan R Calvo

Peptides ◽  
1993 ◽  
Vol 14 (6) ◽  
pp. 1331-1338 ◽  
Author(s):  
Catherine Fabre ◽  
Assou El Battari ◽  
Catherine Bellan ◽  
Eric Pasqualini ◽  
Jacques Marvaldi ◽  
...  

Author(s):  
B. L. Soloff ◽  
T. A. Rado

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.


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