戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 while 11 proteins were identified in the NPM immunocomplex.
2 REST, and the proteins are found in the same immunocomplex.
3 e phosphorylated on tyrosine residues by the immunocomplex.
4 d secondary antibody to form a sandwich-type immunocomplex.
5 ted onto the immunonanobeads thus forming an immunocomplex.
6 crossing, the interaction yields immobilized immunocomplex.
7 the interaction yields a zone of immobilized immunocomplex.
8 trip, resulting in the formation of specific immunocomplex.
9 nfirmed by immunoblotting of hBVR.PKC betaII immunocomplex.
10 ted with 200 nm nanobeads through sandwiched immunocomplexes.
11 ometry that RAD50 protein is present in TRF2 immunocomplexes.
12 rs (Fc epsilon RIIb or CD23) by IgE-allergen immunocomplexes.
13 he CDK inhibitor p21Cip1 present in cyclin E immunocomplexes.
14  modulated by the formation of sandwich-like immunocomplexes.
15 ed by its sequestration into visible MAP4-Ab immunocomplexes.
16 P MS), thus counting individual UCNP-labeled immunocomplexes.
17 ntibody (p53(392)d-Ab) to form sandwich-like immunocomplexes.
18 ng events due to the formation of sandwiched immunocomplexes.
19 ent protein kinase activity observed for ATM immunocomplexes, along with the association of ATM with
20 ion enriched in nucleolar proteins, and this immunocomplex also includes p125, the catalytic subunit
21 bital at pH 8 show improved stability of the immunocomplex and better separation for immunoassay quan
22   Co-stimulation of PBMCs with AQP4-IgG/AQP4 immunocomplex and complement prompts a Th17-biased respo
23 inhibited Cdc25A activity in the Cdc25A-EGFR immunocomplex and consequently caused prolonged EGFR tyr
24              The anti-IC scFv recognizes the immunocomplex and enables the development of noncompetit
25 med mass spectrometric analysis of the NEIL2 immunocomplex and identified Y box-binding (YB-1) protei
26            HSP70 was also found in the WASF3 immunocomplex and inactivation of HSP70 results in desta
27      VBP1, VHL, and p97 coexist in the hMSH4 immunocomplex and regulate the polyubiquitination of hMS
28 rovides the optimal buffer for measuring the immunocomplex and separating it from the free antigen.
29 e, we show that WASF3 is present in the HER2 immunocomplex and suppression of WASF3 function leads to
30               We showed that the size of the immunocomplex and the field strength are the critical fa
31 ng the subsequent magnetic separation of the immunocomplex and the measurement of chemiluminescent si
32 y recognize the formation of hapten-antibody immunocomplexes and can thus be used to develop phage an
33          Consistently, greater proportion of immunocomplexes and number of antibodies per complex for
34 d to mark the surface-bound single NT-proBNP immunocomplexes and recorded with bright-field microscop
35 onoclonal capture antibody and a unique anti-immunocomplex (anti-IC) antibody fragment (scFv) isolate
36  on the unique combination of a generic anti-immunocomplex (anti-IC) single-chain fragment of antibod
37 g the technical challenges of producing anti-immunocomplex antibody.
38 , immobilized zones of fluorescently labeled immunocomplex are subjected to a buffer dilution and mon
39                                    Images of immunocomplexes are presented in the characteristic view
40 application of the noncompetitive phage anti-immunocomplex assay (PHAIA) by converting an existing co
41 o optimize the performance of the phage anti-immunocomplex assay (PHAIA) technology.
42 p a single-step sandwich-type noncompetitive immunocomplex assay.
43 s and can thus be used to develop phage anti-immunocomplex assays (PHAIA) for noncompetitive detectio
44                                          The immunocomplex between a membrane protein, beta2 adrenerg
45 process through formation of a sandwich-type immunocomplex between first anti-p53/p53/ secondary anti
46 receptor (EGFR) promoted the formation of an immunocomplex between PLCgamma and NMDAR subunits.
47 le noncompetitive sandwich-type format using immunocomplex binding phage-borne peptides to detect the
48                              Formation of an immunocomplex brings the chemiluminescent compound and t
49                               ROC1 and APC11 immunocomplexes can catalyze isopeptide ligations to for
50       Finally, as revealed by FLN spectra of immunocomplexed chromophores, pi-pi interactions, rather
51 uffer dilution, while measuring the decay in immunocomplex concentration.
52                          Individual sandwich immunocomplexes consisting of (1) an anti-PSA antibody i
53                    Furthermore, precipitated immunocomplexes contained T-antigen, NF2, and p53, sugge
54                         We confirm here that immunocomplexes containing a tagged version of Mec1 cata
55 red for Ci phosphorylation in vivo, and Cos2-immunocomplexes (Cos2IPs) phosphorylate Ci and contain P
56 y REST to neuronal genes, is present in REST immunocomplexes, dephosphorylates S861/864, and stabiliz
57 ine and parenchymal organs or resulting from immunocomplex deposition due to B cell hyperactivity wit
58 to the known effects of other surfactants in immunocomplex dissociation or in maintenance of colloida
59 ive immunoassays to develop a new Phage Anti-Immunocomplex Electrochemical Immunosensor (PhAIEI) for
60 tein, under optimized condition, forming the immunocomplex FITC-PrA-Ab-PrP.
61        With the aid of a running buffer, the immunocomplexes flow and reach the immuno-conjugated ele
62 tive glomerulonephritis due to deposition of immunocomplexes followed by cardiomegaly with ventricula
63 are mechanisms triggered by antibody-antigen immunocomplexes following fixation of the component 1q (
64                   To quantify kon, we assess immunocomplex formation for a range of antigen-antibody
65 anning results in a very high probability of immunocomplex formation for very low Ag concentrations,
66                              A half-sandwich immunocomplex formation induced high proton conduction,
67                      The successful sandwich immunocomplex formation is then recorded electrochemical
68 ivated macrophages from Nhe1-deficient mice, immunocomplex formation of Nhe1 and FcepsilonR1 in IgE-a
69                  The dose-response curve for immunocomplex formation of TNT on the scFv-functionalize
70                                          The immunocomplex formation was biochemically amplified by e
71 ic peak current in anionic redox probe after immunocomplex formation with antibodies was used for PSA
72 ciple of photoluminescence quenching of upon immunocomplex formation with antibody-functionalized dia
73 orescent phosphopeptide used as a tracer for immunocomplex formation with phosphotyrosine antibody.
74 corporation of electrothermal flows enhances immunocomplex formation, allowing for rapid and sensitiv
75  the enzyme substrate was used to detect the immunocomplex formation.
76 nnels (20 nm pore sized) blockage due to the immunocomplex formation.
77 kon is quantified by assessing the amount of immunocomplex formed at each interaction time.
78 now shows that HSP90 is present in the WASF3 immunocomplex from prostate cancer cells.
79 o uses a handoff mechanism that switches the immunocomplex from the stacking mode to the separation m
80                                        NEIL2 immunocomplexes from cell extracts preferentially repair
81 hotyrosine and anti-c-Src immunoprecipitated immunocomplexes from heated cells.
82                                 In contrast, immunocomplexes from inaC mutants missing eye-PKC, displ
83 on to facilitate the movement of GNP-labeled immunocomplexes from the membrane to the absorption pad,
84 continuously separating the antibody-protein immunocomplexes from the unbound antibodies, utilizing t
85 imultaneously differentiate between free and immunocomplexed haptens.
86                        The IL-2/anti-IL-2 Ab immunocomplex has recently been shown to expand the natu
87       In addition, B2GP1 bound to IgA aB2GP1 immunocomplexes have been described as a marker to predi
88  association of p65 with biologically active immunocomplex-histone acetyltransferase assay was depend
89                                 Furthermore, immunocomplex-histone acetyltransferase assays demonstra
90                          Preformed B2C5-UvrB immunocomplexes, however, inhibited formation of those i
91 r wall of the column, forming the "sandwich" immunocomplexes (immobilized antibody-E. coli O157: H7-e
92 I kappa B alpha can be catalyzed by the ROC1 immunocomplex in vitro.
93  show that the electrophoretic separation of immunocomplexes in free solution can be readily accompli
94 is a more efficient substrate for IKKepsilon immunocomplexes in human FLS and this activity appears t
95                  Two-dimensional averages of immunocomplexes in which the ryanodine receptor was in t
96                                    Wild-type immunocomplexes incubated with [(32)P]ATP revealed phosp
97 c subunit was identified in endogenous FOXO1 immunocomplexes, indicating that PP2A is a FOXO1 phospha
98     To quantify koff, an immobilized zone of immunocomplex is subjected to in situ buffer dilution, w
99                FEN-1 is present in the NEIL1 immunocomplex isolated from human cell extracts, and the
100  it was absent in the LP-BER-proficient APE1 immunocomplex isolated from the mitochondrial extract th
101                Incubation of anti-PLC-gamma1 immunocomplexes isolated from rat brain with recombinant
102 ities were determined by immunochemistry and immunocomplex kinase assay approaches.
103                        Furthermore, in vitro immunocomplex kinase assay with Akt1, a natural substrat
104 f NF-kappaB kinase (IkappaB), as examined by immunocomplex kinase assay, IkappaB phosphorylation, and
105 KC(epsilon) knockout mice and in vitro in an immunocomplex kinase assay, PKC(epsilon) phosphorylated
106                      Unlike the conventional immunocomplex kinase assay, this assay directly utilizes
107   Protein kinase activities were measured by immunocomplex kinase assay.
108                                              Immunocomplex kinase assays demonstrated an IL-1-activat
109                                              Immunocomplex kinase assays with cyclin-dependent kinase
110 ed member-specific antibodies, and performed immunocomplex kinase assays with extracts from elicited
111 scence method, MAPK activity was measured by immunocomplex kinase assays, and Western blot analysis a
112 rmore, incubation of activated ERK2 with FAK immunocomplexes leads to FAK phosphorylation at Ser-910
113                      The assay is a sandwich immunocomplex microarray that functions via excitation b
114 the excited-state vibrational frequencies of immunocomplexed molecules allowing for unambiguous spect
115                                    Then, the immunocomplex of antihuman IgE Abs with the patient IgE
116 g a peptide that specifically recognizes the immunocomplex of atrazine with an anti-atrazine monoclon
117          p185HER2/Neu was also identified in immunocomplexes of c-Src following ligand activation of
118 ng an intact Y-box sequence in CFTR; 6) that immunocomplexes of CDP/cut possess an associated histone
119                                          The immunocomplexes of RIP140 from cells transfected with RI
120 the anti-AQP4 immunoglobulin (AQP4-IgG)/AQP4 immunocomplex on the induction and profile of ex vivo cy
121 y measuring the formation of the fluorescent immunocomplex on the waveguide surface.
122 was dependent on the formation of sandwiched immunocomplexes on the particles.
123                                   The formed immunocomplexes on the test line can further be excised
124 ith specific antibodies and then labeled the immunocomplexes (one or zero labeled target protein mole
125 on of the benefits of integrating phage anti-immunocomplex particles into electrochemical immunosenso
126   In contrast, although present in the NEIL2 immunocomplex, PCNA does not stimulate NEIL2.
127 ein-multipeptide constructs composed of anti-immunocomplex peptides selected from phage libraries and
128 enerated recombinant chimeras by fusing anti-immunocomplex peptides selected from phage libraries to
129 s a scaffold for multivalent display of anti-immunocomplex peptides.
130 to 3-phenoxybenzoic acid (3-PBA) and an anti-immunocomplex phage clone bearing the cyclic peptide CFN
131         The administration of agonistic IL-2 immunocomplexes phenocopies the absence of Tregs, i.e.,
132       Substrate trapping in intact cells and immunocomplex phosphatse assays confirmed that alpha-cat
133  during SM22 gene expression and SRF and CBP immunocomplexes possess HAT activities in smooth muscle
134                                   The mSin3A immunocomplexes possess histone deacetylase activity tha
135                          This Ets-1-CBP/p300 immunocomplex possessed histone acetyltransferase activi
136  assays of kinase activity were performed in immunocomplexes precipitated by an antibody against the
137 to the preconcentration step to separate the immunocomplex products formed.
138  protein were inhibited both in vitro and in immunocomplexes purified from the cell extracts.
139  both Eps8 and TLR4 were present in the same immunocomplex regardless of LPS stimulation.
140  molecular weight proteins in CDK and cyclin immunocomplexes, represent two distinct families constit
141 rticles and antigen was captured, the formed immunocomplex resulted in a decrease of the darkness and
142               Electron microscopic images of immunocomplexes show two antibody binding sites.
143 eaching the test line, where a sandwich-like immunocomplex takes place due to the presence of antibod
144 roduced to the sensing system, forming large immunocomplexes that prevent CL substrate access to the
145 periodic DNA organization in nanocrystalline immunocomplexes that trigger strong recognition by TLR9,
146 that administration of the IL-2/anti-IL-2 Ab immunocomplex to C57BL/6 mice, prior to corneal HSV-1 in
147 itiated by the addition of a PiaA-associated immunocomplex to membranes of TORC2-deficient cells and
148                         The kinase activity (immunocomplex toward S6 peptide) of each isoform was act
149 rmined on days 7 and 16 postinfection in the immunocomplex-treated group of infected mice.
150 rease in NK cell numbers in corneas from the immunocomplex-treated group of mice.
151 eas from the control group, corneas from the immunocomplex-treated group showed a significant reducti
152                                              Immunocomplex treatment given on days 5, 6, and 7 postin
153 roteins were identified as unique to the ALK immunocomplex using monoclonal and polyclonal antibodies
154 In the presence of target cell receptors, an immunocomplex was formed between anti-CD20 antibodies an
155                                          The immunocomplex was performed by using tosylactivated magn
156 eak current of Fe(CN)6(3-)/Fe(CN)6(4-) after immunocomplexed was formed.
157     The activity of p85/p110beta (PI3-Kbeta) immunocomplexes was elevated by increase[Ca2+]e and acti
158 ies and a mass spectroscopic analysis of the immunocomplex, we show the presence of homo- and heterom
159 hat recognize the BDE 47-polyclonal antibody immunocomplex were isolated.
160 s detected from the C-Dots on these sandwich immunocomplexes were positively correlated to the concen
161                                              Immunocomplex Western blotting demonstrated increased as
162 gh the shallow regions easier than the large immunocomplex, when the flow-field is applied in an obli
163 ced by a tyrosine kinase associated with the immunocomplexes, whereas in vitro phosphorylation of rec
164  allowed to interact with each other to form immunocomplexes which are then typically captured by pro
165 specifically react with the analyte-antibody immunocomplex, which allows the detection of these small
166 ity associated with cdk4, cyclin E, and cdk2 immunocomplexes, which normally increases following seru
167 kinase (CDK) inhibitor, p27Kip1, to cyclin E immunocomplexes, which resulted in a reduction in CDK2 k
168 inding to bax since less bax was observed in immunocomplex with bcl-2 in taxol-treated cancer cells.
169 ten healthy controls were cultured with AQP4-immunocomplex with or without complement.
170 ese transcription factors are present in the immunocomplex with purified p53, implicating modificatio
171 Dot-labeled Ab2 was added to form a sandwich immunocomplex with the AFP bound to the Ab1-coated wells
172                                     erbB2 is immunocomplexed with a GPCR in vivo and is transactivate
173        The phosphorylated peptide product is immunocomplexed with the anti-phosphotyrosine antibody r
174 ells, the C/EBPdelta protein was detected in immunocomplexes with both Rb and E2F1.
175 ntibody and enzyme reporter are used to form immunocomplexes with the target protein, which are readi
176   Finally, we found that Galpha(q/11) formed immunocomplexes with the type-A endothelin receptor and

 
Page Top