Fluorescent banding pattern analysis of eight taxa of Phaseolus and Vigna in relation to their phylogenetic relationships

1993 ◽  
Vol 87 (1-2) ◽  
pp. 38-43 ◽  
Author(s):  
J. Y. Zheng ◽  
M. Nakata ◽  
K. Irifune ◽  
R. Tanaka ◽  
H. Morikawa
Keyword(s):  
Banding Pattern ◽  
Phylogenetic Relationships ◽  
Pattern Analysis ◽  
Fluorescent Banding

Fluorescent Banding Pattern and Species-Specific DNA Marker inRumex thyrsiflorusFingerh.

2012 ◽  
Vol 137 (1) ◽  
pp. 70-77 ◽  
Author(s):  
A. Grabowska-Joachimiak ◽  
D. Kwolek ◽  
A. Kula ◽  
P. Marciniuk
Keyword(s):  
Banding Pattern ◽  
Dna Marker ◽  
Fluorescent Banding ◽  
Species Specific

Q-Banding Pattern Analysis of KB Cells

1974 ◽  
Vol 13 (1-2) ◽  
pp. 117-122 ◽  
Author(s):  
C.-C. Lin
Keyword(s):  
Banding Pattern ◽  
Pattern Analysis ◽  
Kb Cells

scholarly journals Differential Fluorescent Banding Pattern in Three Varieties of Cicer arietinum L. (Fabaceae)

CYTOLOGIA ◽  
2005 ◽  
Vol 70 (4) ◽  
pp. 441-445 ◽  
Author(s):  
Shahina Akter ◽  
Sheikh Shamimul Alam
Keyword(s):  
Cicer Arietinum ◽  
Banding Pattern ◽  
Cicer Arietinum L ◽  
Fluorescent Banding

scholarly journals Speckled Fluorescent Banding Pattern in Scorzonera (Asteraceae)

Hereditas ◽  
2004 ◽  
Vol 132 (3) ◽  
pp. 265-267 ◽  
Author(s):  
Giovanni D'Amato
Keyword(s):  
Banding Pattern ◽  
Fluorescent Banding

Telomerase is processive

1991 ◽  
Vol 11 (9) ◽  
pp. 4572-4580
Author(s):  
C W Greider
Keyword(s):  
Banding Pattern ◽  
Tandem Repeats ◽  
Pattern Analysis ◽  
Reaction Products

Telomerase synthesizes tandem repeats of the sequence d(TTGGGG) onto input d(TTGGGG)n primer oligonucleotides (C. W. Greider and E. H. Blackburn, Cell 43:405-413). An intrinsic RNA component of the enzyme provides the template for d(TTGGGG)n repeat synthesis [C. W. Greider and E. H. Blackburn, Nature (London) 337:331-337, 1989; G.-L. Lu, J. D. Bradley, L. D. Attardi, and E. H. Blackburn, Nature (London) 344:126-132, 1990]. In a typical reaction, products greater than 2,000 nucleotides were synthesized in 60 min. Dilution and primer challenge experiments showed that these long products were synthesized processively. The apparent processivity was not due to a higher affinity of the enzyme for long d(TTGGGG) products over the shorter competitors. The degree of processivity was quantitated; telomerase synthesized approximately 520 nucleotides before half of the enzyme had dissociated. After dissociating, telomerase reinitiated d(TTGGGG)n synthesis on new primer oligonucleotides. The products from a telomerase reaction have a characteristic 6-nucleotide banding pattern (C. W. Greider and E. H. Blackburn, Cell 51:887-898, 1987). A strong pause in the reaction occurs after the addition of the first G in the sequence d(TTGGGG). Both the processivity and the banding pattern analysis imply that in the elongation mechanism there must be a translocation step after the 9 nucleotides of internal template RNA have been copied to the extreme 5' end.

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