ライフサイエンスコーパス: cohesive end

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1 nteraction of restriction DNA fragments with cohesive end.

2 zed to one area of the phage genome near one cohesive end.

3 omoter directing transcription away from the cohesive end.

4 Mg(2+) cations stabilize the interaction of cohesive ends.

5 h every combination of possible bases in the cohesive ends.

6 , whereas protected fragments retained their cohesive ends.

7 e breaks and correction of mismatches in the cohesive ends.

8 reassembly involving complementary nanofiber cohesive ends.

9 conditions that greatly favored ligation of cohesive ends, a second DNA fragment could be selectivel

10 The cohesive ends are fully complementary and were either re

11 After nicking, the cohesive ends are separated by terminase; terminase boun

12 y between the CP(+) and CP(-) triple helical cohesive ends at the layer interfaces promotes a (CP(-)/

13 s developed to quantitate repair of defined, cohesive-ended break structures revealed that DSB-induce

14 s alone did not promote efficient joining of cohesive-ended DNA fragments in a cell-free assay.

15 hose of additional experiments indicate that cohesive ended DSBs in chromosomal DNA can be accurately

16 eliminated in diploids, suggesting that the cohesive-ended DSBs could be efficiently repaired by hom

17 The three-base cohesive ends for ligation correspond to the codon for t

18 rly show that DNA restriction fragments with cohesive ends form substantial amount of circles in the

19 ere formed by cyclizing linear DNA with long cohesive ends in the presence of supercoiled molecules.

20 We find that ligation between cohesive ends is highly efficient and does not require t

21 mentary overhangs, and stimulated joining of cohesive ends more than twentyfold.

22 to the downstream cosN to generate the right cohesive end of the chromosome.

23 rotein binds to restriction enzyme-generated cohesive ends of linear fragments and also exhibits some

24 stretching the molecules, which exposes the cohesive ends of the otherwise undeformed lambda-phage D

25 nicks are introduced at cosN to generate the cohesive ends of virion DNA.

26 near DNAs with a terminal duplication of the cohesive-end region, between DR1 and DR2.

27 ATPase activity, though the cos cleavage and cohesive end separation activities were near to those of

28 ode an HNH endonuclease (HNHE) next to their cohesive end site and terminase genes.

29 thermore, we demonstrate that this conferred cohesive end stability is specific for divalent cations,

30 ) with NaCl leads to a near complete loss of cohesive end stability.

31 We further demonstrate that cohesive end stabilization is achieved by substituting M

32 mulates degradation of DNA by Mre11, whereas cohesive ends strongly inhibit it.

33 the form of "modules" having a standardized cohesive end structure.

34 While HMO2 binds DNA with both blunt and cohesive ends, the sequence of a single stranded overhan

35 by combining stable branched DNA motifs with cohesive ends to produce programmed nanomechanical devic

36 s cleavage assay; in this deleted phage, the cohesive ends were not cut.

37 This sequence is found in the left lambda cohesive end, where exonuclease inhibition may contribut

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