ライフサイエンスコーパス: helper phage

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1 n proteins produced from a CTX prophage (its helper phage).

2 ustly with packaging by conventional M13-KO7 helper phage.

3 face, if packaged by the modified M13-KO7(+) helper phage.

4 ing particles using proteins supplied by the helper phage.

5 etic elements that are mobilized by specific helper phages.

6 lls and amplified in vivo in the presence of helper phages.

7 of SaPI1 transducing particles and those of helper phage 80alpha was investigated by direct comparis

8 can be mobilized by infection with S. aureus helper phage 80alpha.

9 In contrast, helper phage activators do not show this increase in tra

10 The helper phage activators have more activity on the P4 pha

11 4 sid promoter, which has more activity with helper phage activators, has a second binding site cente

12 of SaPI excision and replication by certain helper phages and their efficient encapsidation into pha

13 but are nevertheless packaged efficiently by helper phages and transferred at high frequencies.

14 with the phagemids and infected with VCSM13 helper phage, and the resulting AtT-20 cDNA-bacteriophag

15 Using standard technology, helper phage are essential for the replication and assem

16 posed of structural proteins supplied by the helper phage but having smaller capsids.

17 g particles comprise proteins encoded by the helper phage, but have a smaller capsid commensurate wit

18 ssemble phagemid particles as efficiently as helper phage, but without helper phage contamination.

19 We have eliminated the need to add helper phage by using 'bacterial packaging cell lines' t

20 as efficiently as helper phage, but without helper phage contamination.

21 1 is encapsidated in a virion assembled from helper phage-encoded proteins.

22 SaPI1 depends on the helper phage for excision, replication and genome packag

23 These packaging cells eliminate the use of helper phage from phagemid-based selection protocols; re

24 id transcription unit are needed only when a helper phage is present; thus, the satellite phage activ

25 ged into phage-like transducing particles by helper phages like 80alpha or phiNM1.

26 on how they interact and interfere with the helper phage machinery for their own benefit.

27 ge-like particles either by typical pac-type helper phages, or by cos-type phages--i.e., it has both

28 delivery system that utilizes a cell-binding helper phage preselected from a landscape phage display

29 gIII was deleted from two helper phages: R408 and VCSM13, which were then propagat

30 SaPIs also interfere with helper phage reproduction, blocking plaque formation, sh

31 I-encoded mechanisms severely interfere with helper phage reproduction, thereby enhancing survival of

32 arriage of important genes-interference with helper phage reproduction, which could ensure their tran

33 id amplification of cDNA ends (RACE), and by helper phage rescue of unamplified clones.

34 Also, a different helper phage, selected from a phage display library, suc

35 The activators from both satellite and helper phages stimulate transcription from Psid.

36 e of a helper plasmid, rather than exogenous helper phage, to produce single-stranded DNA; (ii) use o

37 nsfer of the island itself requires specific helper phages, transfer of unlinked chromosomal segments

38 e generated lysate (the lysogen inhibits the helper phage used to package the recombinant andenoviral

39 ion protein consisting of adapter GR2 in the helper phage vector.

40 ame phagemid vectors combined with different helper phage vectors.

41 A series of engineered helper phages were constructed to facilitate both displa

42 at exploit the life cycle of their temperate helper phages with elegant precision to enable their rap

43 ms, we compared activators from two P2-like (helper) phages with those encoded by two satellite phage

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