ライフサイエンスコーパス: phage display peptide library

1 lecting mAb to isolate peptide mimics from a phage display peptide library.

2 e biopsies after an i.v. administration of a phage display peptide library.

3 DC-binding peptides were identified using a phage display peptide library.

4 ing peptides identified from a combinatorial phage display peptide library.

5 al capsular polysaccharide by screening of a phage display peptide library.

6 nized by each mAb were selected from several phage display peptide libraries.

7 formans capsular polysaccharide by screening phage display peptide libraries.

8 We used the CL15 monoclonal aCL to screen 17 phage-display peptide libraries.

9 lung adenocarcinoma cell line, H2009, from a phage-displayed peptide library.

10 iochemical properties and peptide binding by phage-displayed peptide libraries.

11 o study the affinity and binding kinetics of phages, displaying peptide libraries.

12 We have previously isolated from a phage-displayed peptide library a cyclic peptide that bi

13 robe for detecting colon cancer, we screened phage display peptide libraries against fresh human colo

14 nces derived from the peptides selected from phage-displayed peptide libraries allows for grouping of

15 Random phage display peptide libraries and affinity selective m

16 g an aggregated mAb as bait for screening of phage display peptide library and identifying those pept

17 c sites throughout the emerin molecule using phage-displayed peptide libraries and has been used to l

18 Here we screened phage-displayed peptide libraries and identified the 13-

19 Phage-displayed peptide libraries and in vitro affinity

20 The convergence of phage-displayed peptide libraries and recombinant viral

21 transposon mutagenesis, synthetic peptides, phage-displayed peptide libraries, and mutant dystrophin

22 but previous work with S1 scanning peptides, phage-displayed peptide libraries, and S1 truncation/del

23 Phage-displayed peptide libraries are a powerful tool to

24 t lesions and tumors by in vivo screening of phage-displayed peptide libraries, asking whether they t

25 hat peptides identified from a combinatorial phage display peptide library assemble preferentially to

26 Peptide mimics isolated from phage display peptide libraries by panning with self-tum

27 ulature in the prostate were identified from phage-displayed peptide libraries by selecting for phage

28 nterfere with its binding to p53 we screened phage display peptide libraries for mdm2 binding phage.

29 of our most protective antibodies, to screen phage display peptide libraries for peptide mimotopes th

30 e screened two variable cysteine-constrained phage-displayed peptide libraries for factor H-binding p

31 We screened a phage-displayed peptide library for peptides that home t

32 Random bacteriophage (phage) display peptide libraries have traditionally been

33 Phage-displayed peptide libraries have been used to isol

34 We report here that phage-displayed peptide libraries have yielded a peptide

35 We discuss the contribution of phage display peptide libraries in determining dominant

36 e immunizing peptide confirms the utility of phage display peptide libraries in generating true molec

37 We previously used phage-displayed peptide libraries in vivo to identify pe

38 Affinity selection of phage display peptide libraries is routinely used for is

39 Towards this goal, we biopanned three phage-displayed peptide libraries on a series of well-de

40 Phage-displayed peptide libraries (pIII and pVIII librar

41 Subsequent analysis of a tryptase-specific, phage display peptide library revealed that recombinant

42 Analysis of a tryptase-specific, phage display peptide library revealed that tryptase bet

43 Epitope mapping, using a phage display peptide library, revealed that cAb29 binds

44 Previously, a phage display peptide library screen identified SM1, a p

45 A mimotope of this antigen, selected from a phage display peptide library screen with an ACA, has be

46 es identified in this study demonstrate that phage-displayed peptide library screens on lipid membran

47 As a proof of concept, we produced phage-displayed peptide libraries Ser-[X]4-Gly-Gly-Gly,

48 We have used phage-displayed peptide libraries to identify novel liga

49 ication, we used four rAbs to probe a random phage-displayed peptide library to determine if epitopes

50 nds capable of removing XNAs, we have used a phage-displayed peptide library to identify a six-amino-

51 urine MRK-16 was used to enrich and screen a phage-displayed peptide library to identify reactive mim

52 peptides (BT1 and BT2) were selected from a phage-displayed peptide library via binding to tetragona

53 Using phage display peptide libraries, we screened for ligands

54 of human leukemia cells with a combinatorial phage display peptide library, we isolated a peptide mot

55 Probing phage-displayed peptide libraries, we identified and cha

56 Using a phage-displayed peptide library, we determined that 24B1

57 Panning of phage display peptide libraries with mAb 763.74 and mAb

58 th a 47-LDA mimotope of GD2, isolated from a phage display peptide library with anti-GD2 mAb 14G2a, i

59 Screening of the X(15) phage display peptide library with the anti-GD2 monoclon

60 f peptides that mimic the LOS by screening a phage-display peptide library with a rabbit Ab specific