ライフサイエンスコーパス: lambda phage

1 , and mouse PrP genes isolated in cosmids or lambda phage.

2 ty of bacteria expressing them to killing by lambda phage.

3 ts of 38 BACs, 45 PACs, 26 PI clones and one lambda phage.

4 mid were challenged with T1, T4, T5, T7, and lambda phage.

5 genetic circuit based on the CI repressor of lambda phage.

6 n of coliphage HK022 excludes superinfecting lambda phage.

7 Escherichia coli and the virulent strain of lambda phage.

8 ges that are related to the Escherichia coli lambda phage.

9 y inserting a small fragment of DNA from the lambda phage.

10 to express yeast proteins on the surface of lambda phage.

11 is methods to a well-studied gene network of lambda-phage.

12 ulation to attack by a high concentration of lambda-phage.

13 e observed in Escherichia coli infected with lambda phages 141, 142, 650, and 651 from the Kohara gen

14 Assay of subclones derived from lambda phage 543 of the Kohara library, which encompasse

15 islands', including Escherichia coli T4 and Lambda phages, although many appear standalone.

16 es recombination between attachment sites on lambda phage and E. coli DNAs.

17 RNA-dependent protein kinase was isolated as lambda phage and P1 phage clones from human genomic DNA

18 pendent protein kinase (PKR) was isolated as lambda phage and P1 phage clones from human genomic DNA

19 yWXD703 DNA was subcloned into lambda phage and sequences of insert ends of the lambda

20 ion as judged by the growth of mutant T4 and lambda phages and by assay of cell-free extracts.

21 ocesses are specific to interactions between lambda-phage and its receptor LamB.

22 ABRB3 and GABRA5 has been constructed in P1, lambda phage, and PAC clones.

23 NA interactions; one derived from the native lambda phage antitermination complex and a second isolat

24 exit channel and is also a likely target for lambda phage antiterminator proteins Q and N, and for ba

25 We utilized a lambda phage-based assay and DNA sequencing for determin

26 The cII mutant frequency determined by a lambda phage-based mutation detection system was not inc

27 nd binding affinities between Stx phages and lambda phage can account for the lower stability of Stx

28 In this method, a lambda phage cDNA expression library is screened by in s

29 To identify CACC-binding proteins, a lambda phage cDNA library derived from a rat insulinoma

30 in mouse embryonic fibroblasts carrying the lambda phage cII transgene.

31 ence was identified and sequenced from three lambda phage clones containing the gene.

32 ra from leptospirosis patients identified 13 lambda phage clones that encode tandem repeats of the 90

33 Recombinant lambda phage clones were isolated that encompass the ful

34 G5-E-A-3', confirming previous studies using lambda phage clones, with the exception that the IGHG5 g

35 otal), was determined from three overlapping lambda phage clones.

36 iolet-inactivated phages, or intraperitoneal lambda phage control mice.

37 ein kinase G substrates in vascular cells, a lambda phage coronary artery smooth muscle cell library

38 In lambda phage crosses, Abc2-modified RecBCD could substit

39 growth slows down, the lytic growth rate of lambda phages decreases, and the propensity for lysogeny

40 The mRNAs were cloned into a lambda phage-derived vector to create the cDNA library.

41 Here we demonstrate the use of lambda-phage displaying Cry1Aa13 toxin variants modified

42 Straightened lambda phage DNA (48 kb) bound to a slide surface was di

43 m both PCR and reverse-transcription PCR for lambda phage DNA and H3 influenza RNA with ramp rates an

44 when a cell-free extract was incubated with lambda phage DNA at 65 degrees C.

45 s, hybrid DNA comprising a large sequence of lambda phage DNA flanked by short pieces of chlamydia DN

46 otic protein required for the integration of lambda phage DNA into its host genome.

47 The elastic response of single plasmid and lambda phage DNA molecules was probed using optical twee

48 rimers that target the sequences of a 650-bp lambda phage DNA segment.

49 DNA toroids produced by the condensation of lambda phage DNA with hexammine cobalt (III) have been i

50 sizes, including Escherichia coli bacteria, lambda phage DNA, and single-stranded DNA fragments as s

51 Using lambda phage DNA, we found that significantly hydrophili

52 two rounds of sorting on E. coli mixed with lambda-phage DNA (10 ng/muL), we demonstrated over 100,0

53 d this system to amplify serial dilutions of lambda-phage DNA (10(5)-10(7) starting copies) and RNA t

54 icrochip device, extraction efficiencies for lambda-phage DNA and human genomic DNA were as high as 6

55 lambda-Phage DNA and M13 were used for the test with goo

56 ed DNA to monitor the enzymatic digestion of lambda-phage DNA by individual bacteriophage lambda exon

57 essful amplification of a 520 bp fragment of lambda-phage DNA in a conventional thermocycler is shown

58 s shown that under any ES conditions, linear lambda-phage DNA is subjected to intensive rupture produ

59 taneous assembly and grouping of end-blunted lambda-phage DNA molecules are negligible.

60 d pulse of light was used to selectively cut lambda-phage DNA molecules at specific restriction sites

61 ffusing fluorescence-labeled double-stranded lambda-phage DNA molecules using dual-color 3-dimensiona

62 nsional tracking microscope to study genomic lambda-phage DNA molecules with various fluorescence lab

63 rate immobilization and stretching of single lambda-phage DNA molecules within microfluidic systems u

64 he cohesive ends of the otherwise undeformed lambda-phage DNA molecules.

65 flow can induce and control the assembly of lambda-phage DNA molecules: increasing shear rates form

66 ensation and decondensation experiments with lambda-phage DNA show that toroid formation and stabilit

67 ght replication of Staphylococcus aureus and lambda-phage DNA targets in under 20 min.

68 etically driven transport of double-stranded lambda-phage DNA through focused ion beam (FIB) milled n

69 Amplification of a 500-base-pair fragment of lambda-phage DNA was achieved in a 1.7-microl chamber co

70 s applied to long DNA molecules (herring and lambda-phage DNA) and revealed that complete dissociatio

71 extraction efficiencies for simple systems (lambda-phage DNA) were approximately 85%, while efficien

72 mposed entirely of the specific H' site from lambda-phage DNA.

73 dye pairs, were constructed from plasmid and lambda phage DNAs.

74 In this work, we demonstrate, using lambda phage dsDNA, that the overstretched states do ind

75 The boxB RNA pentaloops from the P22 and lambda phages each adopt a GNRA tetraloop fold upon bind

76 strategy was used to identify a recombinant lambda phage expressing nuclease activity, and its clone

77 Through screening of a lambda phage expression library, we identified one of th

78 owever, unlike the findings with the related lambda phage, formation of RNA polymerase promoter compl

79 l recognition sequences in the bacterial and lambda phage genome as unique in the way they are bound

80 validated this technology using the 48.5 kb lambda phage genome with different 8-base and 7-base seq

81 ll up to five distinct mutations on a single lambda phage genome without counterselection in only a f

82 LE identifies 12 of 12 synthetic errors in a Lambda Phage genome, surpassing even Pacific Biosciences

83 ntaining these HS were positioned within the lambda phage genome.

84 f IHF bound to another of its sites from the lambda phage genome.

85 uction of recombinant DNA sequences into the lambda-phage genome with 90-100% yield.

86 sequence that was localized on P1-phage and lambda-phage genomic clones by Southern gel-blot analysi

87 light-induced mutations in the cII gene from lambda phage in transgenic mouse embryonic fibroblasts d

88 ll viability relate to phenomena involved in lambda phage induction and excision.

89 that confer a high level of protection from lambda phage infection.

90 own by immunity of Escherichia coli cells to lambda phage infection.

91 A single genetic element, a lambda phage, is the only specialized vector required.

92 phenotypes, which differ significantly from lambda phage itself, driving through in situ recombinati

93 ogen limitation was determined in vivo, in a lambda phage lacZ reporter system integrated as a single

94 ecover host cell-vector DNA junctions from a lambda phage library generated using transduced mouse mu

95 ted adherent cells of lymphocytes by using a lambda phage library method and a long-range PCR techniq

96 hila protein Ags, namely, the screening of a lambda phage library representing the complete L. pneumo

97 re isolated from an A. actinomycetemcomitans lambda phage library.

98 Furthermore, E. coli lambda phage lysogens complemented with B. burgdorferi r

99 rII mutants from growing on Escherichia coli lambda phage lysogens.

100 uggest that the stability of lysogeny in the lambda-phage may be influenced by such extinction phenom

101 When several single lambda phage molecules are subject to the same applied f

102 Adsorption of lambda-phage on sensitive bacteria Escherichia coli is a

103 , the protein prevents complete rezipping of lambda-phage on the 2-s timescale of the experiment, whe

104 such decrease occurred when using methylated lambda phage or M13 duplex DNA.

105 The addition of either linear lambda-phage or plasmid DNA to CLs resulted in an unexpe

106 vestigation, we evaluated the sensitivity of lambda phage PCR on our platform to be less than 2.0 cop

107 ,Zn-SOD demonstrates significant homology to lambda phage proteins, reflecting possible bacteriophage

108 Here, we tested defense against lambda phage provided by Cas12a-crRNAs containing preexi

109 ne the effect of expression heterogeneity of lambda-phage receptors on the response of an Escherichia

110 A highly efficient lambda phage recombination system previously utilized fo

111 ses homologous recombination mediated by the lambda phage Red proteins, to subclone DNA from BACs int

112 The lambda phage repressor is currently used as a genetic to

113 carrying a recoverable, chromosomally based lambda phage shuttle vector designed to report mutations

114 thin a chromosomally integrated, recoverable lambda phage shuttle vector in mouse fibroblasts.

115 We have chosen one of the lambda phage sites, H1, for study because it presents a

116 g the statistical behavior of the well-known lambda phage switch.

117 riming is presented for three DNA templates: Lambda phage, Synechocystis sp. PCC 6803 rbcL gene, and

118 nce reagents, we have cloned (by long PCR or lambda phage techniques) and sequenced 10 near-full-leng

119 erifiable) hypotheses about the mutations of lambda-phage that should change its observable behaviour

120 To test the prediction, an array of isogenic lambda-phages that differ only in their lysis times was

121 to do this, we first demonstrated, using the lambda phage, that long PCR can be made highly sensitive

122 to be less stable than those of the related lambda phage; this is often described in terms of a 'hai

123 pted gene onto the chromosome of E. coli via lambda phage transduction and selecting for kanamycin-re

124 lambda and to facilitate the use of modified lambda phage vectors in mammalian gene transfer applicat

125 repeat sequences into a palindromic clamp in lambda phage we are able to investigate their tendencies

126 For example, lambda phages with an amber mutation in any head gene or

127 Our measurements show that upon incubating lambda-phage with bacteria Ymel, the population of unbou