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 nd a non-ER-containing fraction (250 mM NaCl eluate).
2 ld not be recovered with glycine as the only eluate.
3  adhesion molecules were not detected in the eluate.
4 nt of peptide is conjugated to the generator eluate.
5 tected in the Maxwell eluate than in the EZ2 eluate.
6 e quantitative analysis of solutes in the LC eluate.
7 e proteins are released and recovered in the eluate.
8 C on the basis of the inherent properties of eluates.
9 ompatibility and antimicrobial assessment of eluates.
10  cytometry and Western blot analysis of EGTA eluates.
11 ored only fractionally by addition of column eluates.
12 and anti-Crry Abs were present in glomerular eluates.
13 rification and final preconcentration of the eluates.
14 in standardized duplicate oropharyngeal swab eluates.
15  and endogenous serum components in the BEAD eluates.
16 tibody positive-control (NAb-PC) in the BEAD eluates.
17 ion of the nonresonance Raman spectrum of LC eluates.
18 tion into small-volume (tens of microliters) eluates.
19  set of autoantigens was observed only in RA eluates.
20 al P antigens could be demonstrated in these eluates.
21 erferences; (3) elution/acidification of the eluate; (4) complexation of chromium with 1,5-diphenylca
22 ncentrations (0.1-0.5mM) of EDTA, monitoring eluate absorbance at 280 nm as well as at 215 nm, adding
23                  IgG and IgM combined on DBS eluates achieved a diagnostic sensitivity of 97.9% (95%C
24 ng complex was reconstituted from the column eluate after displacement of SDS with nonionic detergent
25  nanocarriers, Dex was already detectable in eluates after 6h when applying nanocrystals on intact sk
26 synthesized adhesives and the DOX-containing eluates against Streptococcus mutans through agar diffus
27                       The DM-GRASP-Sepharose eluate also contains a potent neurite stimulating activi
28                                       Column eluates also showed some relative concentration of IgG a
29 bands were present in N-acetyl-D-glucosamine eluates, although their % distribution changes in favor
30 s were used for the DBS elutions and the DBS eluate analyses, respectively.
31 automated analysis of lipid extracts and TLC eluates and suggests that indirect high-performace (HP)T
32 ceptor (ER)-containing fraction (150 mM NaCl eluate) and a non-ER-containing fraction (250 mM NaCl el
33 )PFAS ranging between 0.18 and 26 mug L(-1) (eluate) and between 66 and 420 mug kg(-1) (solid).
34 CHO) cell culture supernatant and a purified eluate) and human fluids (i.e., saliva and plasma).
35 ere assessed by ion chromatography in tissue eluates, and the extracellular volume by equilibration o
36 E column, the derivatized phenols in the SPE eluate are analyzed by GC/MS.
37 out further processing the resulting FISHing eluates are suitable for BEAMing (beads, emulsion, ampli
38                                      The DBS eluates are thus free from hematocrit and nonhomogeneity
39 ormed to interpret the DOM chemical space of eluates, as well as permeates and wash liquids with mole
40 ptors apoER2 and Lrp1 were identified in the eluate by mass spectrometry.
41 , called sequential analysis of fractionated eluates by SRM (SAFE-SRM), to plasma from cancer patient
42       Alternatively, conductivity of the DBS eluate can be used for the blood volume determination by
43 ermined by tandem MS of TAP-TbRACK1 affinity eluates, co-sedimentation in a sucrose gradient, and co-
44                          Paired sera and DBS eluates collected from 439 sero-positive, 382 sero-negat
45 orado using serum and dried blood spot (DBS) eluates, compared to ELISA, and evaluated for neutralizi
46                            LC-MS analysis of eluates confirmed DSF retained major cranberry and blueb
47                                  The organic eluate containing extracted analytes was evaporated and
48 (-) mutant was incubated with a pneumococcal eluate containing native PspA, there was decreased depos
49  blend based on polarity into four groups of eluates, corresponding to compounds with zero, one, two,
50                  The absence of DAMGO in the eluate corresponds to a competing MOR ligand in the urin
51 SMR acquired a chromatogram by measuring the eluate density.
52         DNase treatment of IVGG or Id column eluates did not affect anti-Id blocking activity.
53                                     However, eluates did not react with any test cells but did react
54                Importantly, the urea-glycine eluates differed from the conventional eluates in having
55 radiolabeled with (68)Ga by adding generator eluate directly to a vial containing the cold precursors
56 serum samples are carried over to final BEAD eluates due to formation of protein complexes with ADA o
57 C plate dimensions and refined design of the eluate exit system.
58 GFbeta2 treatment elevated IOP and increased eluate fibronectin and PAI-1 content.
59 aman spectroscopy is challenging because the eluate flows fast and limits the accumulation time of we
60 sis of diffusion NMR data measured from HPLC eluate for commercial "monoacetin" (a mixture of glycero
61 ound a higher zinc release in the batch test eluates for all granules, ranging from 15% higher to 687
62 's full automation, and the ability to split eluates for both IVD and LDT testing.
63 red with subsaturating doses of the four IgG eluates for up to 144 hr.
64                                         This eluate fraction stimulated DNA synthesis in quiescent Ba
65 ries of labeled compounds in the appropriate eluate fraction.
66 ibeprin or avebetrin was done using buffered eluate fractions (600-800 MBq, pH 2) of an SnO2-based ge
67                      Subsequently, nanoliter eluate fractions are collected at a rate of one fraction
68           A Western blot (immunoblot) of the eluate fractions revealed a correlation between peak Nef
69                       Column flowthrough and eluate fractions were compared for their ability to bloc
70 ceived AN-102, Cs-depleted effluent, and sRF eluate fractions were comprehensively characterized for
71 biological activity of IL-6 complexes in the eluate fractions were probed using five IL-6 ELISAs and
72    Same complement analysis was performed in eluate from a control column after in vitro perfusion of
73 cal surface compared with incubation with an eluate from a PspA(-) strain.
74  (OCN) is described for direct deposition of eluate from a thermal field-flow fractionation (ThFFF) s
75       A gel activity assay revealed that the eluate from C16-serinol-Sepharose contained three serine
76  both nonreduced and reduced NDNF, while IgG eluate from phospholipase A2 receptor-MN showed no bindi
77                                          The eluate from the first dimension is actively modulated us
78 also detected by far-Western analysis in the eluate from the wild-type RNA column but not from the mu
79                                          The eluate from the wild-type RNA column contained a 65-kDa
80  detected by immunoblot in soluble fractions eluated from RBC units stored for more than 35 days, but
81 tivity was greatly enriched in the high-salt eluates from a D' affinity column.
82 f SLE APAD combining sites was observed with eluates from anti-DNA Id affinity columns; however, no c
83                                           In eluates from both patient and control, immunoadsorbent c
84 rom autoimmune MRL/lpr mice are not found in eluates from class II molecules of MHC-identical C3H mic
85                                              Eluates from donor hearts placed in vimentin/complete Fr
86 and casein (a milk protein) were analyzed in eluates from dried blood spots by enzyme-linked immunoso
87  of 17 inflammatory markers were measured in eluates from dried blood spots using a bead-based multip
88 rdless of child diagnosis, newborn bloodspot eluates from females had a significantly higher concentr
89                                        Using eluates from FLAG-NEIL1 immunoprecipitates from human ce
90                  Western blot analysis using eluates from frozen tissue showed IgG binding to PCSK6 i
91                                              Eluates from gel regions equivalent to 38 kDa were analy
92 i-Id blocking activity was recorded for IVGG eluates from human cationic myeloma columns devoid of th
93                           In two recipients, eluates from immunoadsorbent columns were analyzed for C
94 e-3-phosphate dehydrogenase were absent from eluates from lung and liver.
95  were also recovered from the isothiocyanate eluates from microcystin-Sepharose by a rebinding intera
96 rations of 9 different APPs were measured in eluates from neonatal dried blood spots from cases, cont
97                            Furthermore, acid eluates from recombinant or cellular MR1 proteins enhanc
98 ected above 200 kDa in wheat germ agglutinin eluates from solubilized cells suggests that some recept
99         This protein was not detected in the eluates from the mutant or the antisense RNA columns.
100  sputum specimens) were positive by PCR with eluates from the smears.
101                                              Eluates from the Zymo kits also tested positive for DNA
102 mination, similar in appearance to dsDNA, in eluates from the Zymo, Qiagen, and ChargeSwitch kits.
103                                          The eluates from these kidneys did not contain ANA, anti-dsD
104 lyacrylamide gel electrophoresis analysis of eluates from these supports shows that five polypeptides
105                              Plasma antibody eluates from two patients were used to select for phage
106                        Immunoblotting of the eluate gave a single diffuse band at approximately 73 kD
107            Additional separation within each eluate group was achieved according to the length of the
108 e Sc separation from lanthanides; the column eluate had a Sc enrichment factor of 10.9, with Sc const
109                           The post-processed eluate has been used to radiolabel DOTATOC in yields of
110                  Western blot analyses using eluate IgG of NDNF-MN showed binding to both nonreduced
111         The compartmentalization of the HPLC-eluate in a segmented flow was performed with droplet si
112 immunoprecipitation and concentration of the eluate in the microchannel, IEF-micropillar-MALDI-MS is
113 ycine eluates differed from the conventional eluates in having significantly greater reactivity to gl
114 ion-free protocol for use directly with swab eluates in LAMP assays, thereby eliminating the time and
115 in standardized duplicate oropharyngeal swab eluates, in a modified intention-to-treat population.
116  the residual drug and human IgG in the BEAD eluates indicate that the BEAD efficiently removed the h
117 g site) activity in human anti-DNA Id column eluates indicates that epibodies from IVGG are relativel
118      The SI pump transfers the resulting DBS eluates into CE sample vials through an internal port of
119 ized for online ethanol-postprocessed (68)Ga eluate investigating various parameters, such as buffer
120 After filtration, the amount of DAMGO in the eluate is analyzed by liquid chromatography tandem mass
121            The capillary blood volume in the eluate is calculated from the concentrations of the inor
122 of elution solvent in a sample vial, and the eluate is directly subjected to an automated analysis by
123                                          The eluate is reduced to < 1.0 mL and reconstituted in 10/90
124  hot-cell system,(68)Ga(3+) of the generator eluate is trapped on a cation exchanger cartridge (100 m
125 then eluted, using pH 2.5 glycine-saline and eluates neutralized to pH 7.4.
126  derivatization are: 500muL of isopropanolic eluate obtained by SPE combined with 500muL of derivatiz
127 the other hand, interference was observed in eluate obtained from C18 SPE column.
128 lyses detected anti-FAT1 IgG and IgG4 in the eluate obtained from pooled frozen kidney biopsy tissue
129              Subsequent digestion of the mAb eluate occurred in a pepsin-modified membrane within 5 m
130  step yields a highly concentrated PCR-ready eluate of nucleic acids devoid of PCR inhibitors that ar
131 mately 50-kDa, and 34/31-kDa polypeptides in eluates of CaM affinity columns, suggesting the presence
132  rat hepatoma cells were treated with CE and eluates of CDSF at a range of 1-25 mug/ml.
133                                       CE and eluates of CDSF demonstrated dose-dependent inhibition o
134                                          The eluates of filters showed trapped bacteria determined by
135                                          The eluates of filters used for leukoreduction were also ass
136 sement membrane and western blot analyses of eluates of frozen biopsy tissue to detect binding of IgG
137  Distinct protein compositions were found in eluates of lung and liver extracts processed in a like m
138 -actinin Abs were present in sera and kidney eluates of lupus mice with active nephritis.
139 el electrophoresis of the microcystin-biotin eluates of the three fractions revealed a complex patter
140 tibody against rat HB-EGF indicated that the eluate peak contained immunoreactive proteins of 22 and
141 lls was also tyrosine phosphorylated by this eluate peak.
142           Pretreatment of microvesicles, RBC eluate preparations, and HDL with phosphatidylinositol-s
143        PNH RBC that were exposed to HDL, RBC eluate preparations, or microvesicles demonstrated decre
144               More important, DOX-containing eluates promoted inhibition of MMP-1 activity when compa
145 bber (EPDM) or thermoplastic elastomer (TPE) eluates, reflect the stronger mechanical stress of batch
146 than the resin, generating more concentrated eluate relative to the amount of Pu loaded onto the foam
147   In contrast, immunoblotting of the peptide eluate revealed no copurifying Galphaq/11, Galphai1/2, G
148 te molar mass, size and concentration of the eluate species.
149 tion column to a micro T-junction, where the eluate stream is compartmentalized into picoliter drople
150 pproximately 20 microL/min of the 3.0 mL/min eluate stream to the mass spectrometer, eliminating the
151 ate nanoflow liquid chromatography (nano-LC) eluate streams at high frequencies and high peak resolut
152 tDNA quantities were detected in the Maxwell eluate than in the EZ2 eluate.
153                                              Eluate that was adsorbed to NC1 hexamer from rat glomeru
154                                       Kidney eluate that was depleted of alpha3(IV)NC1 antibodies sti
155 ombinant PP-1C distinguished proteins in the eluates that bound PP-1C from those that bound PP-2AC.
156 ve major polypeptides in the affinity column eluate, the activity of interest was assigned to the pro
157 beled simply by addition of (68)Ga generator eluate to a cold kit.
158 entalization prevents peak dispersion during eluate transport and conserves the chromatographic perfo
159 3.5, 30 min and 2.5 mL for pH, contact time, eluate volume, respectively.
160                 Our experimental analysis of eluate vs feed concentrations of Li and competing ions d
161        The final concentration of DNA in the eluate was 5x10(6), 14x10(6), and 8x10(6) copies/microL
162                                          The eluate was analyzed by capillary LC fractionation follow
163 s, the digest was subjected to HPLC, and the eluate was analyzed for argpyrimidine.
164                                 Each corneal eluate was collected and stored at -70 degrees C until a
165 column (MICC), and error-depleted DNA in the eluate was collected for downstream gene assembly.
166                                          The eluate was concentrated with two consecutive filtration
167                                          The eluate was concentrated, and the phthalate metabolites w
168          After concentration, the calmodulin eluate was further purified by successive high pressure
169 nalytes were extracted and desorbed, and the eluate was introduced in FAAS via nebulization system.
170       The excessive amount of NH(4)Cl in the eluate was removed by sublimation in the presence of sma
171 ushed with sterile saline, and the collected eluate was submitted for PCR amplification of IS6110 seq
172 romycin content of the serum samples and GCF eluates was determined with an agar diffusion bioassay.
173 NA (but not antihistone) reactivity in these eluates was due to cross-reactive anti-dsDNA antibodies.
174 and other components] plus (99m)Tc generator eluate) was examined.
175 t alpha3(IV)NC1 domain, and serum and kidney eluate were examined for antibodies to both native and r
176 ure model using human anterior segments, and eluates were analyzed for fibronectin and PAI-1 content.
177                        None of the adhesives eluates were cytotoxic to the human dental pulp stem cel
178                                     The salt eluates were examined for the presence of both DNA repli
179                                          The eluates were IgM free and > or =95% IgG2.
180                                          The eluates were noncytotoxic in micro-CDC assays.
181 ound peptides were eluted with acid, and the eluates were pooled and submitted to high-pressure liqui
182                                          The eluates were subjected to analysis of total protein, SDS
183                                          All eluates were tested for specificity against a variety of
184 ort of the CE instrument and homogenizes the eluates, whereupon the eluted blood compounds are automa
185 nity for DNA than antibodies also present in eluates which blocked anti-DNA combining sites.
186   Immunoprecipitation of the affinity column eluate with a Galpha(13) antibody demonstrated that 8-Br
187  carinii lysate and the 200 mM methylmannose eluate with antibody against the major surface glycoprot
188 e aim behind this is to obtain analyte-laden eluates with ACN/MeOH (90:10, v/v) in unsupervised mode
189 el and dentin powder were submerged in S-PRG eluate (with borate ion concentration of 100 mM) for 3 h
190 beyed in the range of 0.07-3.0 mug mL(-1) in eluate, with the squared correlation coefficient (R(2))
191 nomolar sensitivity in spiked nasopharyngeal eluates within 5 minutes.
192             Glycosidase digestion of the 2 m eluate yielded protein bands of M(r) 90,000 and 60,000 t

 
Page Top