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.