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

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

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

10 89G and M184V, on DNA copying fidelity in an M13 phage-based forward mutation assay.

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

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

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

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

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

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

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

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

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

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

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

22 M13 phage displaying an in vivo biotinylatable peptide (

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

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

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

26 Here we show M13 phage genetically engineered with tyrosine residues

27 M13 phage have provided scaffolds for nanostructure synt

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

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

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

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

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

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

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

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

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

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

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

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

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

41 The M13 phage procoat protein requires both its signal seque

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

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

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

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

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

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

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

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

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

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

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

53 In addition, M13 phages with genetically incorporated bioactive pepti