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1 sidues 18-21 (nuclear magnetic resonance and epitope mapping).
2 attering, and inhibitory monoclonal antibody epitope mapping.
3 y using ELISA, Western blotting, and peptide epitope mapping.
4  PA were identified by using tetramer-guided epitope mapping.
5 in accordance with the results obtained from epitope mapping.
6 ins of other BoNT subtypes and serotypes for epitope mapping.
7  of responses to synthetic IA-2 peptides and epitope mapping.
8 people were re-obtained for AMA and relative epitope mapping.
9 ative SK, which was consistent with previous epitope mapping.
10 ries provide a rapid alternative for surface epitope mapping.
11 G1 peptides were synthesized for IgA and IgG epitope mapping.
12 nd WbGST by in silico analysis and by linear epitope mapping.
13 st time oxidative labeling has been used for epitope mapping.
14 IRPalpha.D1 binding to CD47 was confirmed by epitope mapping analyses of anti-SIRP Abs.
15                  In this report, we describe epitope mapping analysis of SERCA2a in A/J mice that lea
16                                   A detailed epitope mapping analysis of three of these rhesus antibo
17 q-IgG and -IgM interactions were used in the epitope mapping analysis.
18 ear B-cell epitope, as determined by peptide epitope mapping analysis.
19                              Tetramer-guided epitope mapping and Ag-specific class II tetramers were
20                                              Epitope mapping and binding assays indicated that both L
21                            Using solid-phase epitope mapping and confirmatory assays, we identified s
22                            T-cell responses, epitope mapping and cross-reactivity to profilins (Phl p
23                                              Epitope mapping and database searches revealed the prese
24                                              Epitope mapping and functional studies performed with 17
25                                              Epitope mapping and genetic studies revealed that the an
26                             A combination of epitope mapping and ligation-based PCR methods identifie
27                          Monoclonal antibody epitope mapping and serologic inhibition studies using C
28 ope for RV-A16 and RV-A39 by tetramer-guided epitope mapping and the ability for RV-A16-specific Th1
29                                          STD epitope mapping and trNOESY bioactive conformation analy
30 d multiple approaches including mutagenesis, epitope mapping, and comparisons to primate MCP to make
31 sorbent assay, Western blotting, solid-phase epitope mapping, and competition assays.
32 e personalized allergy diagnostic, allergens epitope mapping, and cross-reactivity studies.
33                                      Titers, epitope mapping, and isotypes of the Abeta42-specific an
34 een 26D1 and H16.V5 was shown using pairwise epitope mapping, and their binding difference is demonst
35 in-ligand interactions and is widely used in epitope mapping, antibody engineering and screening for
36  We studied NKp46D2 by using a peptide-based epitope mapping approach and identified an NKp46D2-deriv
37                            A tetramer-guided epitope mapping approach was used to identify HLA-restri
38                          The tetramer-guided epitope mapping approach was used to identify IGRP-speci
39  using an alanine scanning mutagenesis-based epitope mapping approach.
40 a manner entirely different from traditional epitope mapping approaches.
41      The Fab-Fc complex half-life screen and epitope mapping are potentially useful tools in the scre
42 s therapeutics underscores the importance of epitope mapping as an essential step in characterizing a
43                Using a yeast surface display epitope mapping assay and neutralization escape mutant,
44 ells were determined by a novel CD154 T cell epitope mapping assay.
45           Based on glycosidase digestion and epitope mapping, band 0.03 was hypothesized to represent
46 erization by selection of escape mutants and epitope mapping by flow cytometry analysis of site-direc
47                                      Further epitope mapping by functional group modification establi
48                                              Epitope mapping by phage display analysis indicated that
49                                              Epitope mapping by phage display revealed that both inhi
50  norovirus strains involved in cell binding, epitope mapping by phage display was performed with an M
51                                              Epitope mapping by real-time surface plasmon resonance s
52 development of the novel method differential epitope mapping by STD NMR (DEEP-STD NMR) for identifyin
53       We used an approach of protein surface epitope mapping by synthetic peptides to analyze the sur
54                                          Our epitope mapping data indicate that the organization of Z
55                         This data along with epitope mapping data of anti rHuEPO monoclonals was used
56 s is a simple yet rational strategy based on epitope mapping data to develop a genetically modified h
57 ce constraints, are generated from available epitope mapping data.
58                                              Epitope mapping demonstrated sites on the Na-ASP-2 molec
59                                              Epitope mapping enabled the identification of MHC/T cell
60                                              Epitope mapping experiments demonstrate that the CREB.CB
61                                              Epitope mapping experiments showed that positive control
62 een used to detect KLK4-specific peptides in epitope mapping experiments.
63                                              Epitope-mapping experiments indicated that Wnt1 class-sp
64                                              Epitope mapping for one of the MAbs, which recognizes a
65  different truncated forms of MARCO, allowed epitope mapping for the PLK-1 Ab to MARCO domain V betwe
66                                     Although epitope mapping has identified residues on the human pap
67                                              Epitope mapping identified the N-terminal domain of FH a
68 etween mAbs that were not predicted by prior epitope mapping, identifying 3 distinct neutralization c
69                                         Fine epitope mapping, in which an array of overlapping 13-mer
70 e used a hybrid method approach for antibody epitope mapping, including single-particle cryo-electron
71                                              Epitope mapping indicated MAb 1C3 recognized a region of
72                                              Epitope mapping indicated that a putative nuclear locali
73                                              Epitope mapping indicated that the anti-C2b mAb 3A3.3, w
74                                     Antibody epitope mapping is a key step in understanding antibody-
75                                              Epitope mapping localized the epitope of 3F3A and a comm
76                                          For epitope mapping, Mal d 1-specific T-cell lines were stim
77 opes were determined using a high-throughput epitope mapping method.
78 bactericidal mAb 12C1 was studied by various epitope mapping methods.
79                              Proteomic-based epitope mapping of 11B9/61 monoclonal antibody revealed
80                                              Epitope mapping of 12 monoclonal antibodies (MAbs) direc
81                                              Epitope mapping of 125-2H using human-mouse IL-18 chimer
82                                              Epitope mapping of 42F and 43F by binding to linear pept
83 t the humanization, affinity maturation, and epitope mapping of 8H9 based on structure determination,
84                                              Epitope mapping of a bactericidal anti-GNA33 mAb using o
85 We sought to clone, express, and perform IgA epitope mapping of a CD-specific wheat antigen and to st
86 meric interspecies and homologue muteins and epitope mapping of a monoclonal antibody (MoAb) to the h
87 e of tumor cell lines and subsequent peptide epitope mapping of a NKp30 blocking antibody, we have id
88                                              Epitope mapping of Ab-binding reactivity revealed prefer
89 esion molecule-1 (ICAM-1) binding assays and epitope mapping of activation-sensitive antibodies using
90  demonstrating the potential use of detailed epitope mapping of Ags for staging of the infection, and
91 onfirmed as critical for collagen binding by epitope mapping of an inhibitory phage antibody against
92                        In the present study, epitope mapping of antagonistic anti-gamma(c) monoclonal
93                                              Epitope mapping of anti-ADAMTS13 immunoglobulin G from p
94 ate the basis for this cross-neutralization, epitope mapping of anti-E1E2 antibodies present within a
95                                              Epitope mapping of anti-PfRh4 monoclonal antibodies iden
96 ants transfected into cells and by anti-PAR1 epitope mapping of APC-treated endothelial cells.
97                                       T cell epitope mapping of Art v 6 revealed that it contains onl
98                                          IgE epitope mapping of Bla g 5 revealed that 2 linear N-term
99                       The identification and epitope mapping of broadly neutralizing anti-human immun
100                                         Fine epitope mapping of DRalphabeta1*0401-and DRalphabeta1*04
101                                     Antibody epitope mapping of endogenous dystrophin indicated prote
102  surface antigen (HBsAg) was investigated by epitope mapping of four anti-HBsAg monoclonal antibodies
103  expression system, lambda foo, was used for epitope mapping of human galectin-3.
104                                              Epitope mapping of human monoclonal antibodies (HMAbs) t
105                                              Epitope mapping of IgA anti-PDC-E2 antibodies indicated
106                                              Epitope mapping of IgG autoantibodies against kinectin r
107 ta on more than 900 peptides used for B-cell epitope mapping of immunodominant proteins of Chlamydia
108 ed peptide microarray approach, coupled with epitope mapping of known autoantigens, to identify and c
109                                              Epitope mapping of LipC identified 6 immunodominant epit
110 s characteristic of flavivirus envelopes and epitope mapping of neutralizing antibodies onto the stru
111 investigated by using monoclonal antibodies, epitope mapping of P66 of Borrelia burgdorferi, and DNA
112 ic techniques can provide a new approach for epitope mapping of polysaccharide-binding Abs and sugges
113                                              Epitope mapping of PTRP delineated 4 peptides that can i
114           Our approach involved a systematic epitope mapping of responses to myelin proteolipid prote
115                                              Epitope mapping of sera from CAEV-infected goats localiz
116                                              Epitope mapping of SG/19 revealed that Thr(82) in the be
117             As expected, monoclonal antibody epitope mapping of the lipid-free and lipid-bound 10F6 a
118                                              Epitope mapping of the neutralizing monoclonal antibodie
119                                              Epitope mapping of the three CXCR4 i-bodies AM3-114, AM4
120                                         Fine epitope mapping of therapeutically relevant monoclonal a
121                                              Epitope mapping of these MAbs demonstrates how some E2/E
122                                        Crude epitope mapping of TpN17 and TpN37 showed that multiple
123 arrays were generated to enable the detailed epitope mapping of two monoclonal antibodies known to re
124                                     Antibody epitope mapping of untensioned microfibrils revealed the
125 n of the bicistronic nature of CYP27 mRNA by epitope mapping of uORF1 suggests that translation of CY
126 te, we used random peptide phage display and epitope mapping of VL Len using wild-type and alanine-mu
127                                     Previous epitope-mapping of autoantibodies (AutoAbs) from prostat
128       This study is the first to demonstrate epitope mapping on the three-dimensional structure of th
129 mal sequence diversity is essential, such as epitope mapping or novel receptor identification, combin
130                                              Epitope mapping performed by screening a random peptide
131                                              Epitope mapping performed by selecting and sequencing an
132                                              Epitope mapping revealed an AMA pattern of reactivity to
133                                              Epitope mapping revealed contact residues for CBH-2 and
134                                         Fine epitope mapping revealed differences in antibody specifi
135         Further characterization by antibody epitope mapping revealed differences in the qualitative
136                                              Epitope mapping revealed eight continuous epitopes acces
137                                 T and B cell epitope mapping revealed major and minor T and B cell ep
138 s that share a conserved central region, and epitope mapping revealed T-cell epitopes in this region.
139                               In this study, epitope mapping revealed that 25F10 interacts at site II
140                                              Epitope mapping revealed that Aw3.18 detects a change in
141                                              Epitope mapping revealed that mAb 2G9 recognizes the C t
142                                              Epitope mapping revealed that the humoral anti-EBNA-1 re
143                                              Epitope mapping revealed that they recognize few distinc
144                                              Epitope mapping revealed the presence of overlapping but
145                                              Epitope mapping reveals that cleavage of the pro-piece o
146                         Moreover, a detailed epitope mapping reveals that the conformational epitopes
147 ges over a 12-18-mo period in response to an epitope-mapping series of 265 12-mer peptides of myelin
148 ast, researchers typically choose for B-cell epitope mapping short peptide antigens in antibody bindi
149                                              Epitope mapping showed that 14 of the 16 patients with t
150                                              Epitope mapping showed that CK6 and CK8 bound between re
151                                Linear B cell epitope mapping showed that serum antibodies recognized
152 ent nanobodies were identified, and detailed epitope mapping showed that these bind to distinct, nono
153                                       T cell epitope mapping strategies increasingly rely on algorith
154                            Using the PepScan epitope mapping strategy, a library of 179 potential pep
155                      We also devised a rapid epitope-mapping strategy, which relies on crosslinking m
156 d by competitive mAbs, (3) confirms previous epitope mapping studies and (4) has the potential to ide
157                                              Epitope mapping studies demonstrated the complex nature
158                                              Epitope mapping studies identified antibodies specific f
159   Alanine scanning-based shotgun mutagenesis epitope mapping studies revealed diverse patterns of fin
160                                              Epitope mapping studies revealed that both the cellular
161                                              Epitope mapping studies revealed that the two MAbs were
162                                              Epitope mapping studies revealed that ZIKV-117 recognize
163                                              Epitope mapping studies revealed the presence of HLA cla
164                                              Epitope mapping studies showed that Ab responses in mice
165 data are consistent with results of previous epitope mapping studies showing that Mabs 25D2 and 35F2
166                                              Epitope mapping studies using competition analysis showe
167                                       T cell epitope mapping studies using IFN-gamma ELISPOT was perf
168                                Comprehensive epitope mapping studies with 166 E protein DIII-LR varia
169 s (MAbs) against the toxin and used them for epitope mapping studies.
170 founding artifacts when IgM Abs are used for epitope mapping studies.
171 otein in the virion, which supports previous epitope mapping studies.
172               We have taken advantage of our epitope-mapping studies of the E2 components of PDC, BCO
173                                              Epitope-mapping studies revealed that these hydrophilic
174                                              Epitope-mapping studies using neutralization escape muta
175 proteins were employed to perform monoclonal epitope-mapping studies with three LPS-blocking Abs that
176 ponse against this virus, we performed a CTL epitope mapping study of JCV VP1 major capsid protein by
177                                    A binding epitope mapping study on clone 1121 and one of the paren
178                                        In an epitope mapping study using biotinylated peptides, all t
179                                              Epitope mapping suggests that all these mAbs recognize c
180 e multichannel pipet form a highly efficient epitope mapping system.
181 he structural topography of IpaD, the Geysen epitope-mapping system was used to identify epitopes rec
182    Collectively, these data show that linear epitope mapping techniques provide useful but incomplete
183  have now been identified using a variety of epitope mapping techniques, including fragmentation by t
184  and assess the potential of the most common epitope mapping techniques, we generated a series of mAb
185  nine residues long and is more efficient in epitope mapping than random peptide libraries.
186 munoassay, where it was demonstrated through epitope mapping that mAb 11-1F4 recognizes a conformatio
187                                              Epitope mapping the specific residues of an antibody/ant
188                            Combined with the epitope mapping, these results indicate portions of the
189  been implicated by mutagenesis and antibody epitope mapping to play a key role in gp120 association.
190 combinatorial phage display-based approach ("epitope mapping") to select peptides binding to the orig
191                                       T cell epitope mapping unveiled a 13-residue sequence conserved
192                                              Epitope mapping using a comprehensive shotgun mutagenesi
193                                              Epitope mapping using activation-sensitive antibodies su
194                The method is based on binary epitope mapping using anti-peptide antibodies.
195                                              Epitope mapping using limited proteolysis, reversed phas
196                                              Epitope mapping using solution nuclear magnetic resonanc
197                                              Epitope mapping using surface plasmon resonance in a BIA
198                                              Epitope mapping, using a phage display peptide library,
199  Analyses of the functional consequences and epitope mapping, using both fluid phase and solid phase
200 fied by peptide/MHC class II tetramer-guided epitope mapping, validated by direct ex vivo enumeration
201                            In such a manner, epitope mapping was applied to the complex interactions
202                                              Epitope mapping was performed by pepscan analysis, site-
203                                              Epitope mapping was performed by sequencing of antibody-
204                                        Using epitope mapping, we discovered mouse monoclonal antibodi
205 respective formulation solutions and antigen epitope mapping were also evaluated.
206 08 of human PrP and have characterized it by epitope mapping, Western immunoblot analysis, and immuno
207                                     Detailed epitope mapping will provide the information needed for
208                                 In addition, epitope mapping with a phage-displayed random peptide li
209                                              Epitope mapping with Ca2+-dependent monoclonal antibodie
210                                     Based on epitope mapping with huntingtin-specific antibodies, we
211                                              Epitope mapping with mammalian and bacterially expressed
212 s with alternative protein constructs and by epitope mapping with peptides covering the identified re
213 -cell epitopes bind antibodies poorly; thus, epitope mapping with short peptide antigens falsely clas
214                                              Epitope mapping with synthetic peptides and electrophili
215                                              Epitope mapping with synthetic peptides revealed that MA
216                                              Epitope mapping with this monoclonal antibody identifies
217 mologs of known sequence were used to refine epitope mapping, with some epitopes ultimately confirmed
218 e inoculated with wild-type Ad recognized an epitope mapping within E1B.

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