ライフサイエンスコーパス: random peptide library

1 identified using a filamentous bacteriophage random peptide library.

2 icroglobulin in the presence or absence of a random peptide library.

3 talytic site of DMPK using a phage-displayed random peptide library.

4 rosine kinase (PTK) by screening a secondary random peptide library.

5 ecipients, using recombinant phages encoding random peptide libraries.

6 nd is more efficient in epitope mapping than random peptide libraries.

7 gh-throughput screening of a phage-displayed random peptide library and classified the cell lines acc

8 sing a genetic selection, we have screened a random peptide library and identified a group of C-termi

9 Epitope mapping performed by screening a random peptide library and in silico docking modeling su

10 We have utilized phage display random peptide libraries as a source of small peptide li

11 ons relations, we designed a phage-displayed random peptide library based on previous knowledge of st

12 /I/L/P/S/G-X-X-X-X-X-X-V/I/L) in vitro using Random Peptide Library-based MHC I LC-MS/MS analysis.

13 We have displayed a 12-amino-acid (12-mer) random peptide library between the H and I sheets of the

14 of synthetic peptides as well as a screen of random peptide libraries by the yeast two-hybrid system.

15 odon sequence was previously isolated from a random peptide library by binding to growth hormone bind

16 stigate protein interactions of FXI, a large random peptide library consisting of 10(6) to 10(7) pept

17 es in SK, we used unconstrained 15 and 6-mer random peptide libraries displayed on phage (theoretical

18 Pools of disulfide-constrained random peptide libraries displayed on phage were selecte

19 elective enrichment from two phage-displayed random peptide libraries enabled us to isolate and ident

20 The sequential screening of random peptide libraries, followed by the evaluation of

21 We have screened a phage-displayed random peptide library for binding to C3b, the proteolyt

22 In this study, we used random peptide libraries from 7- to 13-mers and studied

23 ces, but will also allow the construction of random peptide libraries from which specific binding act

24 esides natural peptide ligands, screening of random peptide libraries has yielded novel bioactive pep

25 uccess reemphasizes the utility of searching random peptide libraries in protein design projects, and

26 Here, by selecting combinatorial random peptide libraries in tumor-bearing mice, we uncov

27 In this study, a random peptide library in which peptide sequences are di

28 a motif was established by the panning of a random peptide library in which peptide sequences are di

29 Peptides selected from random peptide libraries, in which the phage-displayed p

30 The use of synthetic random peptide libraries is a powerful technology for th

31 was previously isolated by biopanning with a random peptide library on filamentous phage.

32 ding peptides by screening a phage-displayed random peptide library on purified NG2.

33 Qa-1 that had been folded in the presence of random peptide libraries or pools of Qdm derivatives ran

34 Affinity selection of random peptide libraries recovered a number of sequences

35 tion, epitope mapping with a phage-displayed random peptide library revealed that one of these mAbs (

36 Accordingly, we screened random peptide libraries (RPLs) displayed on phage with

37 recognized by LIM domains, we have utilized random peptide library selection, the yeast two-hybrid s

38 itochondria, and that an internalizing-phage random peptide library selects for peptide motifs that l

39 istance were selected from in vivo expressed random peptide libraries to study structural features im

40 Here we used a bacterial random peptide library to examine the structural require

41 rget-assisted iterative screening applied to random peptide libraries unveiled a novel and atypical r

42 tein-DNA interactions can be identified from random peptide libraries using phage display techniques.

43 To overcome these obstacles, we screened random peptide libraries using sera from HIV-infected su

44 and (000-1) substrates, were selected from a random peptide library using the phage display technique

45 A 23-mer random peptide library was displayed in the context of t

46 A random peptide library was expressed on the surface of a

47 A 12-mer random peptide library was screened against EGFRvIII.

48 Interaction of two random peptide libraries with glutathione S-transferase-

49 We screened a random peptide library within the receptor-binding domai