ライフサイエンスコーパス: M13 phage

1 led geneV-geneVII intercistronic region from M13 phage.

2 oli from acting as a host for propagation of M13 phage.

3 ersion of this domain (HBDt) into a modified M13 phage.

4 ex with naive peptide libraries displayed on M13 phage.

5 ayed as Fd coat protein fusion constructs of M13 phage.

6 ability to replicate a UV-irradiated form I M13 phage.

7 or nanobody on the pIII or pVIII protein of M13 phage.

8 We took advantage of two unique features of M13 phage, a non-toxic nanofiber-like virus, to generate

9 not defective in reactivation of methylated M13 phage and did not enhance the defect of an alkB muta

10 SICS is here demonstrated on unlabeled M13 phages and on unlabeled NPs with diameters of 210 nm

11 ghly evolved biomaterials such as engineered M13 phages and opens upon a new direction for developing

12 molecules and biomacromolecules by using the M13 phage as the building module to order the assembly o

13 A highly sensitive and selective non-lytic M13 phage-based electrochemical impedance spectroscopy (

14 89G and M184V, on DNA copying fidelity in an M13 phage-based forward mutation assay.

15 pose the simple method for fabricating novel M13 phage-based SPR sensor system which has a high sensi

16 Our M13 phage-based SPR sensor takes advantage of simplicity

17 Furthermore, the sensitivity of the M13 phage-based SPR sensor was enhanced due to the align

18 give superior selectivity and sensitivity to M13 phage-based SPR sensor.

19 We present a new generation of M13 phage-based vectors termed transmorphic phage/adeno-

20 The M13 phage, belonging to the family inoviridae, has a len

21 Using M13 phage display and next generation sequencing, we obs

22 A 9-mer pVIII M13 phage display library is screened against U937 to id

23 , HPVHHYQ and LPLTPLP, were selected through M13 phage display.

24 he isolation of a FN-binding peptide, S2, by M13 phage display.

25 Here we report results from a random M13-phage display library screening to isolate 12-mer pe

26 e past year, methods for the construction of M13 phage-display libraries have been significantly impr

27 Reaction between M13 phage-displayed library of peptides terminated with

28 A panel of M13 phage-displayed peptide ligands with varying affinit

29 M13 phage displaying an in vivo biotinylatable peptide (

30 ecB protein cleaves circular single-stranded M13 phage DNA, but RecB1-929, comprising only the 100 kD

31 We created libraries of recombinant M13 phages expressing receptor-binding proteins based on

32 We have previously utilized an M13 phage expression system and codon-based mutagenesis

33 inities of related antibodies produced in an M13 phage expression system.

34 Here we show M13 phage genetically engineered with tyrosine residues

35 M13 phage have provided scaffolds for nanostructure synt

36 ting assembly of chiral colloidal particles (M13 phage) into functional materials.

37 -assembly of genetically engineered viruses (M13 phage) into target-specific, colourimetric biosensor

38 The major coat protein (pVIII) of M13 phage is of particular interest to structure biologi

39 decrease the fidelity of replication in the M13 phage mutation assay.

40 The resulting azo-M13-phage nanowire exhibits reversible photo-responsive

41 The photo-responsive properties of the azo-M13-phage nanowires may open the door for the developmen

42 The binding of E. coli to the M13 phage on the cytosensor surface increased the charge

43 n antibodies (scFv) that can be displayed on M13 phage or expressed as soluble protein.

44 ximately 140 binding sites are available per M13 phage particle.

45 ive assay is based on the use of recombinant M13 phage particles bearing a peptide that specifically

46 The CVL consisted of M13 phage particles covalently anchored to a 3 mm diamet

47 surface of glassy carbon electrode, and the M13 phage particles were immobilized on them using 3-mer

48 The mutants were displayed on M13 phage particles, and binding to chemokine was assess

49 peptides fused to proteins as well as to the M13 phage, paving the way to phage display of novel bicy

50 a combinatorial peptide library expressed on M13 phage pIII protein to identify peptides that prefere

51 The M13 phage Procoat protein is one of the best characteriz

52 The M13 phage procoat protein requires both its signal seque

53 t function-that can be linked to conditional M13 phage replication.

54 metagenome-inspired library displayed on the M13 phage scaffold, when subjected to a short selection

55 M13 Phages showing less non-specific REE binding without

56 gh we were unable to display the Trp cage on M13 phage, successful display was achieved using the lyt

57 s peptide substrates are co-displayed on the M13 phage surface as fusions to the phage capsid protein

58 ed mutations in the major coat protein P8 of M13 phage that greatly increase the surface display of m

59 After the directional assembly of M13 phage, the D(H) of the probes was significantly incr

60 on to the gene III minor coat protein of the M13 phage, the sequence contained two TGA stop codons in

61 a egf domain was displayed on the surface of M13 phage to facilitate mutagenic analysis and optimize

62 ection platform that links the life cycle of M13 phage to target protein binding through proximity-de

63 used to mimic the closed circular, ssDNA in M13 phage, upon removal of the detergent.

64 Random mutagenesis was carried out within an M13 phage vector by hybridization mutagenesis, and the p

65 ng this library of humanized BR96 Fabs in an M13 phage vector, we rapidly identified several candidat

66 Moreover, compared with existing M13 phage vectors, TPA particles can accommodate large s

67 ultiple cloning sites of the pUC plasmid and M13 phage vectors.

68 The M13 phage was radiolabeled with (99m)Tc via mercaptoacet

69 s is particularly true for the Ff (f1, fd or M13) phages, which represent a widely distributed group

70 In addition, M13 phages with genetically incorporated bioactive pepti