scholarly journals M13 phage DNA probe informativity rising at studying pig genome

1996 ◽  
Vol 12 (3) ◽  
pp. 64-66
Author(s):  
K. F. Pochernayev ◽  
K. I. Kiynitsa ◽  
G. D. Telegeev ◽  
M. V. Dybkov ◽  
S. S. Malyuta
Keyword(s):  
1990 ◽  
Vol 18 (4) ◽  
pp. 1065-1065 ◽  
Author(s):  
Phil Chen ◽  
Nicholas K. Hayward ◽  
Chev Kidson ◽  
Kay A.O. Ellem

1990 ◽  
Vol 45 (4) ◽  
pp. 687-690 ◽  
Author(s):  
Nicholas Hayward ◽  
Philip Chen ◽  
Derek Nancarrow ◽  
John Kearsley ◽  
Peter Smith ◽  
...  

1993 ◽  
Vol 9 (1) ◽  
pp. 51-53
Author(s):  
A. I. Martsinkovskaya ◽  
V. L. Motin ◽  
R. S. Mukhamedov ◽  
A. A. Abdoukarimov

1988 ◽  
Vol 47 (2) ◽  
pp. 231-240 ◽  
Author(s):  
A. Ito ◽  
F. T. Robb ◽  
J. G. Peak ◽  
M. J. Peak
Keyword(s):  

FEBS Letters ◽  
1988 ◽  
Vol 233 (2) ◽  
pp. 388-392 ◽  
Author(s):  
A.P. Ryskov ◽  
A.G. Jincharadze ◽  
M.I. Prosnyak ◽  
P.L. Ivanov ◽  
S.A. Limborska

Author(s):  
Dhruba K. Chattoraj ◽  
Ross B. Inman

Electron microscopy of replicating intermediates has been quite useful in understanding the mechanism of DNA replication in DNA molecules of bacteriophage, mitochondria and plasmids. The use of partial denaturation mapping has made the tool more powerful by providing a frame of reference by which the position of the replicating forks in bacteriophage DNA can be determined on the circular replicating molecules. This provided an easy means to find the origin and direction of replication in λ and P2 phage DNA molecules. DNA of temperate E. coli phage 186 was found to have an unique denaturation map and encouraged us to look into its mode of replication.


Author(s):  
Gary Bassell ◽  
Robert H. Singer

We have been investigating the spatial distribution of nucleic acids intracellularly using in situ hybridization. The use of non-isotopic nucleotide analogs incorporated into the DNA probe allows the detection of the probe at its site of hybridization within the cell. This approach therefore is compatible with the high resolution available by electron microscopy. Biotinated or digoxigenated probe can be detected by antibodies conjugated to colloidal gold. Because mRNA serves as a template for the probe fragments, the colloidal gold particles are detected as arrays which allow it to be unequivocally distinguished from background.


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