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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
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
29 bands were present in N-acetyl-D-glucosamine eluates, although their % distribution changes in favor
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
35 ere assessed by ion chromatography in tissue eluates, and the extracellular volume by equilibration o
37 out further processing the resulting FISHing eluates are suitable for BEAMing (beads, emulsion, ampli
39 ormed to interpret the DOM chemical space of eluates, as well as permeates and wash liquids with mole
41 , called sequential analysis of fractionated eluates by SRM (SAFE-SRM), to plasma from cancer patient
43 ermined by tandem MS of TAP-TbRACK1 affinity eluates, co-sedimentation in a sucrose gradient, and co-
45 orado using serum and dried blood spot (DBS) eluates, compared to ELISA, and evaluated for neutralizi
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,
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
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
66 ibeprin or avebetrin was done using buffered eluate fractions (600-800 MBq, pH 2) of an SnO2-based ge
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
74 (OCN) is described for direct deposition of eluate from a thermal field-flow fractionation (ThFFF) s
76 both nonreduced and reduced NDNF, while IgG eluate from phospholipase A2 receptor-MN showed no bindi
78 also detected by far-Western analysis in the eluate from the wild-type RNA column but not from the mu
80 detected by immunoblot in soluble fractions eluated from RBC units stored for more than 35 days, but
82 f SLE APAD combining sites was observed with eluates from anti-DNA Id affinity columns; however, no c
84 rom autoimmune MRL/lpr mice are not found in eluates from class II molecules of MHC-identical C3H mic
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
92 i-Id blocking activity was recorded for IVGG eluates from human cationic myeloma columns devoid of th
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
98 ected above 200 kDa in wheat germ agglutinin eluates from solubilized cells suggests that some recept
102 mination, similar in appearance to dsDNA, in eluates from the Zymo, Qiagen, and ChargeSwitch kits.
104 lyacrylamide gel electrophoresis analysis of eluates from these supports shows that five polypeptides
108 e Sc separation from lanthanides; the column eluate had a Sc enrichment factor of 10.9, with Sc const
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
122 of elution solvent in a sample vial, and the eluate is directly subjected to an automated analysis by
124 hot-cell system,(68)Ga(3+) of the generator eluate is trapped on a cation exchanger cartridge (100 m
126 derivatization are: 500muL of isopropanolic eluate obtained by SPE combined with 500muL of derivatiz
128 lyses detected anti-FAT1 IgG and IgG4 in the eluate obtained from pooled frozen kidney biopsy tissue
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
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
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
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
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
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
158 entalization prevents peak dispersion during eluate transport and conserves the chromatographic perfo
169 nalytes were extracted and desorbed, and the eluate was introduced in FAAS via nebulization system.
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.
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.
181 ound peptides were eluted with acid, and the eluates were pooled and submitted to high-pressure liqui
184 ort of the CE instrument and homogenizes the eluates, whereupon the eluted blood compounds are automa
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))