ライフサイエンスコーパス: biopanning

1 is-specific peptide ligands by phage display biopanning.

2 ovalently bound small peptide discovered via biopanning.

3 mid particles, during library production and biopanning.

4 PYNHNWFAL was selected after three rounds of biopanning.

5 Laminin-1 derivatized plates were used for biopanning.

6 Through repeated biopanning, 103 peptidyl sequences were identified, many

7 high-density peptide microarray derived from biopanning a lung cancer phage display library.

8 r consisted of an icosapeptide identified by biopanning a phage display library against Ad5 knob.

9 Here, we achieve spatial control by biopanning a phage library to discover materials that ta

10 From an initial phage display biopanning, a series of peptide ligands for the LDLR was

11 Conversely, biopanning against four mAbs did not yield any frameshif

12 Biopanning and rapid analysis of selective interactive l

13 the repertoire, in combination with in vivo biopanning at optimized phage circulation time, we have

14 After three rounds of biopanning by 1E4 from the phage display library, a mime

15 Three rounds of biopanning C-34 against the library resulted in striking

16 , cell-specific peptides isolated from phage biopanning can be used for the discovery of cell surface

17 III protein of filamentous phage was used in biopanning experiments against several protein targets.

18 This is the first comprehensive biopanning for isolation of high affinity peptidic ligan

19 This is the first comprehensive biopanning for the isolation of TM transiting peptidic l

20 After two rounds of biopanning, >90% of the clones recovered were specifical

21 Biopanning has been used extensively in conjunction with

22 er peptide, identified through phage display biopanning, has been used for the first time to induce t

23 Phage display biopanning identified Gly-Ile-Arg-Leu-Arg-Gly (GIRLRG) a

24 PL biopanning is also unbiased with regard to pathogens or

25 We show that, compared to conventional biopanning methods, microfluidic selection enables more

26 reast with high titer IgG autoantibodies for biopanning of a T7 phage breast cancer cDNA display libr

27 over, we report the first successful in vivo biopanning of AAV capsids by using a new AAV-DJ-derived

28 This high-throughput selection involved biopanning of an ovarian cancer phage display library us

29 demonstrate that peptides obtained from the biopanning of phage display libraries can be readily use

30 After three or six rounds of biopanning on either Ab, positive phage-displayed Ags re

31 By direct biopanning on HUVECs and a second approach involving pre

32 These results demonstrate the utility of biopanning on isolated cells for identifying specific bi

33 Several rounds of biopanning on NG2 resulted in the specific enrichment of

34 Anti-PSMA Nanobodies were captured by biopanning on PSMA-overexpressing cells.

35 new approach, termed "protection-linked (PL) biopanning," probes the Ab paratopes of protected vaccin

36 se (type V) (TRAP) was used as the bait in a biopanning procedure.

37 ty of cystatins can be used in phage display biopanning procedures to select variants with greater in

38 A biopanning process designed to find peptide epitopes spe

39 Although techniques such as biopanning rely heavily upon the screening of randomized

40 After three successive biopanning rounds, a panel of six clones with distinct g

41 g recombinant scN proteins were subjected to biopanning selection based on binding affinity to immobi

42 ustrating the potential of phage display and biopanning selection for directed molecular evolution of

43 These results show that in vivo biopanning selection in hypercholesterolemic animals mak

44 Papain biopanning selection of phage-displayed soyacystatins re

45 We used two M13-bacteriophage display biopanning strategies to search for mediators of trans-T

46 M2pep, identified using a subtractive phage biopanning strategy against whole cells.

47 We describe here a new in vivo biopanning strategy in which a human phage single-chain

48 Our data highlight the power of the new PL-biopanning strategy to identify Ab responses with signif

49 the target antigen morphology using a novel biopanning technique that utilizes atomic force microsco

50 The phage library was used in an in vivo biopanning technique to identify non-DNA-binding, kidney

51 nzymatic processing steps into phage display biopanning to expand the biocombinatorial procedure and

52 This demonstrates the potential to use biopanning to generate capture ligands for a large varie

53 Through biopanning using gut tissue from larvae of the non-targe

54 erived from affinity-enrichment experiments (biopanning) using a filamentous phage peptide library.

55 s, in vivo bone marrow/cardiac phage display biopanning was performed and led to the identification o

56 btain heart-targeting ligands, phage display biopanning was used to isolate a 20-mer peptide that bin

57 After PL biopanning, we analyzed the phagotopes selected for amin

58 ing genetic immunization, phage display, and biopanning, we identified two functional monovalent Abs

59 oE knockout mice was interrogated by in vivo biopanning with a phage-displayed constrained peptidyl l

60 ence, called H10, was previously isolated by biopanning with a random peptide library on filamentous

61 ge-displayed tumor antigens were enriched by biopanning with normal and then SCCHN-specific serum.

62 Biopanning with three different sera led to the cloning