ライフサイエンスコーパス: T7 phage

1 cessful display was achieved using the lytic T7 phage.

2 played library generated from C4-2B cells in T7 phage.

3 used to construct a phage display library in T7 phage.

4 s C approach levels observed using wild-type T7 phage.

5 4 protein that cannot support the growth of T7 phage.

6 otifs in the receptor binding protein of the T7 phage.

7 strategy for quantifying miRNAs by employing T7 phage-a bacteria-specific virus nanoparticle-as a sur

8 T7 phage also express a 56-kDa truncated gp4 lacking the

9 genes for their ability to inhibit growth of T7 phage and >90% of the host genes for their ability to

10 of the portal complexes of Phi29, SPP1, T3, T7 phages and herpes simplex virus.

11 nuclease subunits, EcoKI is inhibited by the T7 phage antirestriction protein ocr, a DNA mimic.

12 Prior work has demonstrated that T7 phages are bound in the outermost curli polymer layer

13 titer IgG autoantibodies for biopanning of a T7 phage breast cancer cDNA display library.

14 ivates the toxin AriB until triggered by the T7 phage counterdefence protein Ocr.

15 Together, these findings suggest that T7 phage display can be used to rapidly and selectively

16 ing a high-throughput method, we developed a T7 phage display cDNA library derived from mRNA isolated

17 For this, we generated T7 phage display libraries of N-terminally and C-termina

18 deployed a customized P. falciparum PhIP-seq T7 phage display library containing 238,068 tiled 62-ami

19 sis antigens, we developed a high-throughput T7 phage display library derived from the sarcoidosis cD

20 n be identified through immunocreenings of a T7 phage display library with high accuracy, which may h

21 A T7 phage display screen against full-length human ERalph

22 Through the use of a T7 phage display, we discovered a novel interaction betw

23 e in vitro genetic selection method based on T7 phage display.

24 to achieve successful in vitro selection of T7 phage-displayed peptides that recognize markers expre

25 consistent with cryo-electron micrographs of T7 phage DNA.

26 en applied to a library of 65,536 engineered T7 phages, each carrying randomized riboswitch variants.

27 The T7 phage-encoded small protein Gp2 is a non-DNA-binding

28 roughput method involved the assembly of 938 T7 phages encoding potential breast cancer autoantigens.

29 ene Expression and Selection (PHEIGES) using T7 phage genome and Escherichia coli TXTL.

30 T7 phage gp4 protein also drives DNA branch migration, s

31 Although T7 phage grow better when both forms are present, the ro

32 amino acid substitution(s) in this region on T7 phage growth and on the interaction of the polymerase

33 We show here that inhibition of T7 phage growth by udk overexpression can be overcome by

34 oduct inhibits host RNA polymerase, restores T7 phage growth on hosts overexpressing udk.

35 e, which explains why A257T does not support T7 phage growth.

36 establish an all-cell-free viral cycle where T7 phages infect synthetic cells, equipped with lipopoly

37 T7 phage is a lytic phage with a broad host range specif

38 d are inefficient in complementing growth of T7 phage lacking gene 3.

39 able the 56-kDa gp4 to support the growth of T7 phage lacking gene 4 (T7Delta4).

40 containing these mutations cannot complement T7 phage lacking gene 4 for T7 growth.

41 the altered proteins to complement growth of T7 phage lacking gene 4.

42 lyzed for their ability to support growth of T7 phage lacking gene 4.

43 yielded a protein that could not complement T7 phage lacking gene 5 (T7Delta5) to grow on E. coli ha

44 eduction in its ability to support growth of T7 phage lacking gene 5.

45 Infection of Escherichia coli by the T7 phage leads to rapid and selective inhibition of the

46 in a model study using low-diversity peptide T7 phage library with spiked-in brain homing phage demon

47 al genome is transcribed by a single-subunit T7 phage-like RNA polymerase (mtRNAP), structurally unre

48 We isolated 95 T7 phage mutants that were resistant to ddT.

49 t RNA polymerase, restores the burst size of T7 phage on udk-overexpressing hosts to normal.

50 ability of short interfering RNAs, including T7 phage polymerase-synthesized RNA (PRNA), which like s

51 istidine fusion protein under control of the T7 phage promoter was expressed in HT-1080 cells and UMR

52 We describe here an RNA, derived from the T7 phage R1.1 RNase III substrate, that is resistant to

53 l role of every residue in the tip domain of T7 phage RBP (1660 variants) by developing a high-throug

54 When gene 1.7 was expressed from a plasmid, T7 phage resistant to ddT still arose; analysis of 36 of

55 placed from the template strand by an active T7 phage RNA polymerase.

56 We track each cycle step to demonstrate T7 phage-specific adsorption onto the liposomes, genome

57 roof-of-concept for the use of bioengineered T7 phage strains to increase the sensitivity of phage am

58 Overexpression using the vaccinia virus/T7 phage system resulted in secretion of approximately 3

59 Selection of T7 phage that can recognize these altered receptors has

60 e mRNA as bait, we could selectively amplify T7 phage that display either the spliceosomal protein U1

61 However, T7 phages that grow at a similar rate provided with eith

62 Using the ability of T7 phage to replicate in nitrogen-starved bacteria as a

63 ng protein, over the detection of replicated T7 phage viron itself, and a greater then 100-fold incre

64 A synthesis in cells infected with wild-type T7 phage was inhibited by ddT, suggesting that it result

65 age of B. malayi expressed on the surface of T7 phage was sequentially screened with sera samples fro

66 ploiting the Ocr antirestriction function of T7 phage, which completely prevents degradation of unmet

67 a coli and Vibrio cholerae under exposure to T7 phages, which we study using microfluidic culture, hi

68 T7 phage with gene 2.5 deleted can grow only on Escheric