scholarly journals Construction and Analysis of Two Genome-Scale Deletion Libraries for Bacillus subtilis

Cell Systems ◽  
2017 ◽  
Vol 4 (3) ◽  
pp. 291-305.e7 ◽  
Author(s):  
Byoung-Mo Koo ◽  
George Kritikos ◽  
Jeremiah D. Farelli ◽  
Horia Todor ◽  
Kenneth Tong ◽  
...  
2004 ◽  
Vol 5 (1/2) ◽  
pp. 103-109 ◽  
Author(s):  
S. Moy ◽  
L. Dieckman ◽  
M. Schiffer ◽  
N. Maltsev ◽  
G.-X. Yu ◽  
...  

2017 ◽  
Vol 10 (1) ◽  
Author(s):  
Paola Randazzo ◽  
Anne Aucouturier ◽  
Olivier Delumeau ◽  
Sandrine Auger

2009 ◽  
Vol 10 (6) ◽  
pp. R69 ◽  
Author(s):  
Christopher S Henry ◽  
Jenifer F Zinner ◽  
Matthew P Cohoon ◽  
Rick L Stevens

2002 ◽  
Vol 46 (1) ◽  
pp. 25-36 ◽  
Author(s):  
Céline Fabret ◽  
S. Dusko Ehrlich ◽  
Philippe Noirot

2010 ◽  
Vol 65 (1) ◽  
pp. 574-580 ◽  
Author(s):  
Tunçer H. Özdamar ◽  
Birgül Şentürk ◽  
Özge D. Yılmaz ◽  
Pınar Kocabaş ◽  
Güzide Çalık ◽  
...  

Author(s):  
Dwight Anderson ◽  
Charlene Peterson ◽  
Gursaran Notani ◽  
Bernard Reilly

The protein product of cistron 3 of Bacillus subtilis bacteriophage Ø29 is essential for viral DNA synthesis and is covalently bound to the 5’-termini of the Ø29 DNA. When the DNA-protein complex is cleaved with a restriction endonuclease, the protein is bound to the two terminal fragments. The 28,000 dalton protein can be visualized by electron microscopy as a small dot and often is seen only when two ends are in apposition as in multimers or in glutaraldehyde-fixed aggregates. We sought to improve the visibility of these small proteins by use of antibody labeling.


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