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1  hCD20-specific antibodies in four rounds of panning.
2 ive antigens after as few as three rounds of panning.
3 purified from FVB/N mouse stomachs by lectin panning.
4 t sufficiently high to allow purification by panning.
5 raries of rANP-display phage by differential panning.
6 d a 195-fold enrichment after five cycles of panning.
7 minant cells into the supernatant, like gold panning.
8 , was more than 100-fold increased after the panning.
9 ide Y, following screening by solution phage panning.
10 imized by using phage display and cell-based panning.
11 specificity of the interaction identified by panning.
12            After three rounds of subtractive panning, 239 of 673 clones analyzed bound selectively to
13  Nipah virus (NiV) and Hendra virus (HeV) by panning a large nonimmune antibody library against a sol
14  anti-Akt1 single-chain antibodies (scFv) by panning a mouse phage-displayed scFv recombinant antibod
15 fied a TREM2 agonist monoclonal Ab (Ab18) by panning a phage-displayed single-chain variable fragment
16 isplay format and make it ideally suited for panning a wide variety of target antigens.
17                                    From this panning, a C-terminal fragment of FGF-BP1 (amino acids 1
18 r muscle-targeting capsids by direct in vivo panning after tail vein injection in mice.
19 ainst fresh neutrophils and independently by panning against a fixed cell line.
20                                              Panning against bovine trypsin resulted in enrichment of
21                       Phage were selected by panning against digoxin, gitoxin (16-OH), and 16-acetylg
22 able fragments (scFvs) after three rounds of panning against FAP.
23  high-affinity human mAb, ANA15, selected by panning against fresh neutrophils and independently by p
24 ide phage display libraries using whole-cell panning against human melanoma cell line Me6652/4.
25 eased iRBC cytoadhesion activity by repeated panning against human umbilical vein endothelial cells (
26 (scFv) phage-display library was used in bio-panning against live, native spores of Bacillus subtilis
27 s from peptide-presenting phage libraries by panning against primary patient CLL cancer cells.
28                                              Panning against rat trypsin resulted in enrichment as we
29                                              Panning against rat trypsin resulted in enrichment but n
30                                 In contrast, panning against secreted EBO glycoprotein (SGP) resulted
31 nesis of its heavy-chain variable domain and panning against sGHeV.
32 0 cDNA-bacteriophage library was enriched by panning against solid- and solution-phase PAI-1.
33 cted from a human nonimmune phage library by panning against the chimeric construct N(CCG)-gp41 (whic
34 age-displayed Fab, scFv, and VH libraries by panning against the receptor binding domain (RBD) of the
35 specific cPTMs are significantly enriched in panning against the specific targets.
36 ry binding site of ecotin, was generated for panning against uPA and rat trypsin.
37                                              Panning against uPA resulted in enrichment as well as th
38  methodological innovation, termed iterative panning and blocking (IPAB), to extend the range of spec
39  the surface of 1264 and BEAS cells used for panning and counter-selection was estimated as 75,000 +/
40                            A direct in vitro panning and enzyme-linked immunosorbent assay-based sele
41 d signaling networks with dynamical zooming, panning and linking capabilities.
42 derpin this diverse functionality, molecular panning and mass spectrometry are used to identify prote
43 s that could be missed by conventional phage panning and screening methods.
44 y bound or eluted phage at various stages of panning and screening procedures.
45                      We use a solution-based panning and screening strategy conducted in the presence
46                                     Repeated panning and selection experiments against a 15-mer pepti
47 ystin LR and its selection using competitive panning and two novel panning strategies.
48 ionary dual-view imaging device with optical panning and zooming capabilities.
49        SurfaceSlide users can perform direct panning and zooming operations on digitised slide images
50  was provisionally mapped by peptide display panning, and a peptide sequence matching the epitope was
51  addition, offer the flexibility of zooming, panning, and being adjustable for slow image acquisition
52 lly support Tat transactivation was used for panning, and of the five unique anti-hCyclinT1 sFvs that
53       Here we applied an in vitro whole cell panning approach using antibody phage display technology
54                         Through a whole-cell panning approach, we previously identified a panel of an
55                     By this "epitope-blocked panning" approach, two novel Fabs, encoded by unique VH
56  an efficiency that exceeds surface-confined panning approaches; and (3) the co-detection of ssDNAs,
57 rovide a intuitive interface for zooming and panning around digital images.
58  and function of CHIP, we report an antibody panning campaign that yielded six recombinant Fabs with
59                          Optical zooming and panning capabilities facilitate repositioning of the zoo
60                          Thus, phage library panning combined with expression cloning permits identif
61 VVYV) from phage display libraries using six panning conditions.
62 selection by tailoring the stringency of the panning conditions.
63                  Here, phage-peptide library panning coupled with screening using next generation seq
64  the antigenic profile of the cells used for panning determines the specificity of the preponderant p
65 ith a streamlined strategy for phage display panning enable the rapid isolation and identification of
66                Incorporating in silico cross-panning enabled computational prescreening of specificit
67             Phage recovered from this second panning exhibited a motif (Ser-His-Tyr) that was subsequ
68                 Sequencing data of the phage panning experiment are deposited at NIH's Sequence Read
69                       Using M13qPCR in phage-panning experiments on live leukemia and prostate cancer
70 ior to candidates derived from phage display panning experiments.
71 lection of this peptide in multiple reported panning experiments.
72 kat libraries enabled repeated screening and panning for antigen-reactive TCRs using peptide major hi
73 (NAR) s that bind to the S2 subunit by phage panning from a naive nurse shark V(NAR) phage display li
74 ns to be propagated as either phage for more panning from repertoires or expressed as soluble sdAb fo
75 ptides, Bicycle, inhibitors of human ACE2 by panning highly diverse bacteriophage display libraries.
76                                            A panning in microtiter plates resulted in 22 unique in vi
77 nique in vitro neutralizing antibodies and a panning in solution combined with a functional neutraliz
78                         After five rounds of panning, individual positive scFv clones were used to in
79 ii) selected functional recombinant phage by panning; (iv) purified the ScFv peptide; (v) shown that
80 ociated retinal cells by a modified two-step panning method and were cultured in serum-free medium co
81                Here, we use a novel cysteine panning method to identify the second cleavage site (Sit
82 ostnatal days 7 and 8 by a modified two-step panning method.
83 may not be accessible by conventional B cell panning methods.
84  through a phage display library and by (ii) panning multiple libraries encoding structurally distinc
85 phage-displayed heavy chain-only antibody by panning of a large (size, approximately 1.5x10(10)) huma
86 dra G (sG) which was used as the antigen for panning of a large naive human antibody library.
87                                     Affinity panning of a library of humanized A4.6.1 antibody mutant
88 dy FC5 was previously isolated by phenotypic panning of a naive llama single-domain antibody phage di
89        To this end, we utilized a sequential panning of a phage library on cultured rat EpiSCs and th
90 in soluble CD4 (sCD4) were alternated during panning of a phage-displayed human antibody library; the
91  G(M3)-derived reagents and their use in the panning of a phage-displayed human single-chain Fv (scFv
92 tence of such a motif was established by the panning of a random peptide library in which peptide seq
93 ssive molecule CD200 were identified by cell panning of an antibody phage display library derived fro
94                         Thus, direct in vivo panning of capsid libraries is a simple tool for the de-
95                                              Panning of IEs on HBMECs led to a more dispersed binding
96  motifs that bind to GroEL by using affinity panning of immobilised GroEL minichaperones for a librar
97 er of structure-based design with sequential panning of large D1 mutant libraries against different H
98                                     Affinity panning of large libraries is a powerful tool to identif
99                                              Panning of phage display peptide libraries with mAb 763.
100                                              Panning of phage Fab libraries against purified antigens
101  regions of arrestin that bind to rhodopsin: panning of phage-displayed arrestin fragments against RP
102                                              Panning of such libraries enriched strongly peptides wit
103                                              Panning of the hot spot libraries yielded several mutant
104                                      Initial panning of the library isolated only non-pathogenic scFv
105 1.7 x 10(4) sequences obtained from repeated panning of the library.
106                                     Affinity panning of these resulted in the selection of variants w
107 patients to receive phage library for serial panning of tumor targeting ligands.
108 n (within 6 d of availability of antigen for panning) of potent mAbs shows the value of large antibod
109 ingle-chain Fv antibody fragments (ScFvs) by panning on a prothrombin-coated surface.
110                                           By panning on B chain, we identified binders and have chara
111                                              Panning on carbonic anhydrase yielded a potent ligand, s
112  antibodies directly from phage libraries by panning on cells.
113 ffinities for digoxin increased 2-4-fold, by panning on digoxin-BSA yet retaining the specificity shi
114  approach involving preclearing steps before panning on HUVECs, we isolated and sequenced 140 individ
115                        After three rounds of panning on recombinant mesothelin, a single-chain Fv (sc
116 on of profiles the phage library enriched by panning on the pool of cancer sera.
117 -specific T cells from animals with SGVHD by panning or by flow cytometric sorting.
118 odologies that rely on microdissection, cell panning or cell sorting, the TRAP methodology bypasses t
119                                              Panning peptide phage display libraries led to the ident
120                             A third round of panning performed in the presence of both the fibrinogen
121 trate, S-adenosylmethionine (AdoMet), during panning permitted PIMT to retain aged phage in greater n
122  The CERVIGTGWVRC sequence was identified by panning phage display libraries on the inhibitory CD47 m
123 tended to specific application of M13qPCR in panning phage libraries on tissue sections of prostate a
124 e sera were then enriched using a multi-step panning procedure.
125 riments performed on this library during the panning process, this scFv bound 1200-fold less tightly
126 ealed by blockade of this epitope during the panning process.
127 es a number of aspects of conventional phage-panning protocols.
128 sequences that reacted specifically to their panning rAb by enzyme-linked immunosorbent assay.
129  we have demonstrated that a synthetic G(M3) panning reagent can be used to isolate a fully human scF
130                                  The initial panning recovered phage that bore the consensus motif Gl
131                                     However, panning rounds are followed by the tedious re-screening
132 body binding phages was observed after three panning rounds, and sequence analysis of randomly select
133 ycoproteins (Envs) dubbed sequential antigen panning (SAP).
134 on of binders to conserved Env structures by panning sequentially against Envs from different isolate
135      Six phage clones identified from S-20-4 panning showed significant binding to both S-20-4 and A-
136  to identify drivers of vascular invasion by panning small hairpin RNA (shRNA) library-transduced non
137 hlight the importance of exploring different panning strategies to optimize the selection of antihapt
138  against DT from two different phage display panning strategies using a human immune library.
139 om a panel of 11 Fabs recovered by different panning strategies, three highly potent neutralizing ant
140 tion using competitive panning and two novel panning strategies.
141            We utilised a novel phage display panning strategy to isolate a high affinity pool (KD ran
142 e positive clones and by using a subtractive panning strategy to remove crossreactivity with B. liche
143 ntigen receptors (PC-CARs) through a counter panning strategy using predicted potentially cross-react
144 ric antigen receptors (CARs) using a counter-panning strategy with predicted potentially cross-reacti
145 rized nonimmune human Ab-phage library and a panning strategy with proteoliposomes and cells to ident
146 play antibody library by using an exhaustive-panning strategy.
147 en, and failure of clonal enrichment by cell panning suggested that the neoantigen was not membrane e
148  of the scFv fragments that were isolated by panning synthetic Ab libraries with different melanoma c
149 the variable region (scFvs) were isolated by panning synthetic scFv library 1 on purified HMW-MAA.
150      This was the first report of a modified panning technique to isolate adult pig RGCs.
151 ated from other retinal tissue by a modified panning technique using Thy 1.1 antibody.
152                        The antigens used for panning the antibodies comprised two soluble, disulfide-
153 cFv library of the melanoma patient and then panning the libraries against melanoma cells to enrich f
154 ce homologies between peptides obtained from panning the library against the antibodies and the nativ
155 ice, measuring Ab responses to immunization, panning the phage library, high-throughput screening of
156 fragment of the V region (scFv) fragments by panning the synthetic phage Ab library (#1) with the hum
157 n any detectable MV Ags; after six rounds of panning, the positive clones comprised 34% of all phage
158                                              Panning this library against PAb1620 resulted in three u
159  in Java that supports real-time zooming and panning through a genome; layout of genomic features and
160 bs, a representative Fab was included during panning to block this common epitope on the F Ag.
161                    By applying phage display panning to hundreds of bacterial genotypes and analyzing
162       We screened a phage library in vivo by panning to identify peptides that bound the vascular end
163                                   Subsequent panning trials using this library yielded promising hits
164 n of VHHs recognizing BDE-47 was achieved by panning under carefully modified conditions.
165  stable C(H)3 heterodimers were recovered by panning using an anti-flag antibody.
166                            A second round of panning was performed against the same target mixture in
167 ner(s) for sperm acrosomal ligands, affinity panning was performed with mouse oocyte lysates using sp
168                    In three patients, repeat panning was possible using phage recovered and amplified
169 rified by counterflow elutriation and lectin panning, was validated by real-time quantitative reverse
170                                  Using phage panning we have also identified several short peptide se
171 wing rounds of selection and deep mutational panning, we identified a high-fidelity peptide consensus
172 ens from immunized mice and in vitro library panning, we identified two antibodies, 2A4 and 1G12.2A4
173           The tool offers smooth zooming and panning which is more flexible than seen in other browse
174 d to search for tumor-associated antigens by panning with a lung adenocarcinoma cell line, 1264, and
175                                        Yeast panning with a nonimmune human single-chain antibody lib
176                                              Panning with an allogeneic breast cancer cell line enric
177 population in the spleens enriched either by panning with anti-guinea pig immunoglobulin G-coated pla
178                                     However, panning with autologous tumor tissue lysate increased bi
179                                           By panning with DNA, the SLE libraries each yielded IgG ant
180                        Selection of phage by panning with fixed neutrophils yielded a 195-fold enrich
181  from 7- to 15mer phage display libraries by panning with hyaluronan-Sepharose beads and assayed for
182 elected from randomly generated libraries by panning with recombinant SCR1-2, followed by specific li
183 ated from phage display peptide libraries by panning with self-tumor-associated Ag (TAA)-specific mAb
184 r EGFRvIII was isolated from this library by panning with successively decreasing amounts of syntheti
185 quid cultures 24 hours after HIV exposure by panning with the ICH3 CD34 MoAb (ICH3/CD34+) and maintai
186             In the last round (round two) of panning with this library, none of the phage clones that
187 nsitions, instead offering smoothly animated panning, zooming, navigation, and track selection.

 
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