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1 imental conditions examined as determined by gel permeation and sedimentation equilibrium analysis.
2 geneity by a combination of acid extraction, gel permeation, and ion-exchange chromatographies.
3                 PM proteins were purified by gel permeation, anion exchange, and NPA affinity chromat
4                                          The gel-permeation behavior of PLA2 at premicellar alkyl sul
5                   We have combined MALDI and gel permeation chromatography (GPC) analyses for broad P
6       Their structures were characterized by gel permeation chromatography (GPC) and (1)H nuclear mag
7 The final cleanup procedure consisted of (i) gel permeation chromatography (GPC) and adsorption chrom
8 y (1)H NMR and UV absorption spectroscopies, gel permeation chromatography (GPC) and light scattering
9                                              Gel permeation chromatography (GPC) and matrix-assisted
10 r of primary amino groups were determined by gel permeation chromatography (GPC) and potentiometric t
11 tracted with ethyl acetate and purified with gel permeation chromatography (GPC) and primary/secondar
12 ess-strain mechanical measurement, (1)H NMR, gel permeation chromatography (GPC) and thermogravimetri
13 [4+2] cycloaddition reaction, as observed by gel permeation chromatography (GPC) and UV-vis spectrosc
14 on rely on measuring the molecular weight by gel permeation chromatography (GPC) based on polystyrene
15 alytical parameter in polymer analysis, with gel permeation chromatography (GPC) being the most commo
16                                              Gel permeation chromatography (GPC) is a generally appli
17 in, we have developed a simple and versatile gel permeation chromatography (GPC) methodology for mole
18 confirm more than 99 % DMAC conversion while gel permeation chromatography (GPC) studies indicate wel
19 d the polydispersity index was determined by gel permeation chromatography (GPC) to be as low as 1.34
20 of-flight mass spectrometry (ESI-TOF MS) and gel permeation chromatography (GPC) were used to study t
21 ze challenging 2D-LC workflows: (1) coupling gel permeation chromatography (GPC) with reversed-phase
22                                              Gel permeation chromatography (GPC), (1)H NMR spectrosco
23                     X-ray diffraction (XRD), gel permeation chromatography (GPC), and electron parama
24 R) spectroscopy, infrared (IR) spectroscopy, gel permeation chromatography (GPC), and high-resolution
25 om polyolefin separation techniques, such as gel permeation chromatography (GPC), crystallization elu
26 on of the polymer cyclic topology comes from gel permeation chromatography (GPC), dynamic light scatt
27 gh-Performance Liquid Chromatography (HPLC), Gel permeation chromatography (GPC), Fourier Transform I
28 e primary tool used to determine plastic MW, gel permeation chromatography (GPC), has major limitatio
29 -NIR absorption/fluorescence spectroscopies, gel permeation chromatography (GPC), NMR, and DFT simula
30     The degradation process was monitored by gel permeation chromatography (GPC), scanning electron m
31 rstanding of the bias-inducing mechanisms in gel permeation chromatography (GPC), the magnitude of er
32 persity index (PDI) of 1.6, as determined by gel permeation chromatography (GPC).
33 olymer was confirmed by (1)H NMR spectra and gel permeation chromatography (GPC).
34 performance liquid chromatography (HPLC) and gel permeation chromatography (GPC).
35 g electron microscopy, pharmacokinetics, and gel permeation chromatography analyses at various time p
36                                              Gel permeation chromatography analysis and molecular ima
37                                              Gel permeation chromatography analysis confirmed that de
38 ode of action was observed and studied using gel permeation chromatography and (1)H NMR.
39 accharides were purified by using Bio-Gel P4 gel permeation chromatography and characterized by nucle
40                                           In gel permeation chromatography and cross-linking experime
41                                  Analysis by gel permeation chromatography and fluorescence spectrosc
42                   They were characterized by gel permeation chromatography and had very low polydispe
43  as DNA separation matrixes were measured by gel permeation chromatography and multiangle laser light
44                                              Gel permeation chromatography and native gel electrophor
45 igh molecular mass ISA complexes resolved by gel permeation chromatography and native-polyacrylamide
46 discrete size (<4 x 10(6) Da) as measured by gel permeation chromatography and remain intact after di
47                                              Gel permeation chromatography and sedimentation equilibr
48     Six young red wines were fractionated by gel permeation chromatography and subsequently each frac
49 action products isolated from barley malt by gel permeation chromatography and ultrafiltration on the
50 ent molecular mass of 600 kDa as measured by gel permeation chromatography and, like the membranes of
51                                              Gel permeation chromatography confirmed that polymer was
52                                              Gel permeation chromatography confirmed that the Asp-280
53                                              Gel permeation chromatography coupled with multiangle la
54                                              Gel permeation chromatography data for the oxidized lign
55                                Consequently, gel permeation chromatography data for the polymers can
56                                              Gel permeation chromatography demonstrated that (alpha-S
57 n reaction products using immunoblotting and gel permeation chromatography demonstrated that PC2 can
58                              Multi-detection gel permeation chromatography enabled the determination
59 ar weight distributions similar to those for gel permeation chromatography for polyethylene polymers,
60                                              Gel permeation chromatography identified a unique 328 kD
61 a, SSIII, BEIIa, and BEIIb all comigrated in gel permeation chromatography in a high molecular mass f
62                                              Gel permeation chromatography in the presence of 0.2% n-
63                                              Gel permeation chromatography indicated that N2, N3, and
64 th FeSO4, phenylalanine, and DTT followed by gel permeation chromatography leads to an iron-hydroxyla
65                                              Gel permeation chromatography of an oligomer preparation
66 tron-paramagnetic resonance spectroscopy and gel permeation chromatography of cryomilled samples, in
67 lation with either DMS or MMPA coeluted upon gel permeation chromatography of extracts of acetate-gro
68                                              Gel permeation chromatography of full-length hDlg reveal
69                                              Gel permeation chromatography of isolated ball-milled li
70 rom wild-type L-FABP (+/+) mice, isolated by gel permeation chromatography of liver soluble proteins,
71  by nuclear magnetic resonance spectroscopy, gel permeation chromatography of polymers extracted from
72                                              Gel permeation chromatography of solubilized microsomes
73                                        Using gel permeation chromatography of the clinical grade hCG
74 olymers and DNA by means of electrophoresis, gel permeation chromatography or filtration exploits siz
75 rial properties and is generally analyzed by gel permeation chromatography or more recently, by MALDI
76 ysis of purified preparations of FBS AChE by gel permeation chromatography revealed the presence of a
77 tering measurements on proteins separated by gel permeation chromatography showed a small amount of h
78                 Analyses of degraded PEOs by gel permeation chromatography showed that the fungus cle
79                                              Gel permeation chromatography sub-fractionation of the c
80                                              Gel permeation chromatography supported a conformational
81 tron paramagnetic resonance spectroscopy and gel permeation chromatography under a variety of experim
82 ion followed by a clean-up of the extract by gel permeation chromatography was performed.
83                                In this study gel permeation chromatography was used to resolve calciu
84 tron paramagnetic resonance spectroscopy and gel permeation chromatography were employed to study the
85 esonance spectroscopy, X-ray diffraction and gel permeation chromatography were used to monitor the c
86               Polymers were characterized by gel permeation chromatography with multiangle laser ligh
87 cular weight of 91 kDa that co-eluted during gel permeation chromatography with plastidial CT and ACC
88 A combination of lectin, anion exchange, and gel permeation chromatography yielded milligram quantiti
89  cyclic polymer product was characterized by gel permeation chromatography, (1)H NMR spectroscopy, an
90  partition coefficient (K(av)) measured with gel permeation chromatography, a high hydrodynamic radiu
91 ed a panel of biophysical methods, including gel permeation chromatography, analytical ultracentrifug
92  bind melittin was assessed using analytical gel permeation chromatography, analytical ultracentrifug
93 alyzed using X-ray microcomputed tomography, gel permeation chromatography, and (1)H-nuclear magnetic
94 s synthesized and characterized by (1)H NMR, gel permeation chromatography, and differential scanning
95  domains by circular dichroism spectroscopy, gel permeation chromatography, and intrinsic viscosity d
96 lly characterized using 1H NMR spectroscopy, gel permeation chromatography, and oligosaccharide profi
97             Three fractions are separated by gel permeation chromatography, and the first fraction co
98  desorption/ionization mass spectrometry and gel permeation chromatography, confirming successful mol
99                                              Gel permeation chromatography, nondenaturing polyacrylam
100 I peptide hydrolysate was fractionated using gel permeation chromatography, OFFGEL isoelectric focusi
101  and alphaA-R116C-crystallin were studied by gel permeation chromatography, SDS-polyacrylamide gel el
102                                           By gel permeation chromatography, the size of the PI-PLC-re
103 clear magnetic resonance characterization of gel permeation chromatography-fractionated acetylated ma
104 tely C6H11SiH3 approximately C8H15SiH3, with gel permeation chromatography-multi-angle laser light sc
105  molecular weights were determined by tandem gel permeation chromatography-multiangle laser light sca
106 itated with ethanol, and further purified by gel permeation chromatography.
107 vity co-purifies with ACCase activity during gel permeation chromatography.
108 ntly associated dimer during ion-exchange or gel permeation chromatography.
109 sacylase activity are partially separated by gel permeation chromatography.
110 aponified and the bulky PC-8 was enriched by gel permeation chromatography.
111 ents with laser diffraction spectroscopy and gel permeation chromatography.
112 um albumin, ion exchange chromatography, and gel permeation chromatography.
113 tes were determined by mass spectrometry and gel permeation chromatography.
114        Synthesized polymers were analyzed by gel permeation chromatography.
115 s of all four proteins were also detected by gel permeation chromatography.
116 e manufacturers' reported values obtained by gel permeation chromatography.
117  with manufacturers' values as determined by gel permeation chromatography.
118 heir hydrodynamic properties as evidenced by gel permeation chromatography.
119 polydispersity index of 1.2 as determined by gel permeation chromatography.
120 ngle-walled carbon nanotubes (s-SWNTs) using gel permeation chromatography.
121 d wild-type mice were analyzed by sequential gel permeation chromatography/acid-urea polyacrylamide g
122 raction of initiated catalyst using standard gel-permeation chromatography (GPC).
123 lar weight distributions, as demonstrated by gel-permeation chromatography and (1)H NMR spectroscopy.
124 ecipitation, ammonium sulfate precipitation, gel-permeation chromatography and concanavalin-A-Sepharo
125 The same process is further characterized by gel-permeation chromatography and fluorescence resonance
126  whole cell-wall nuclear magnetic resonance, gel-permeation chromatography and transcriptome sequenci
127 ss of the APPL by over 50%, as determined by gel-permeation chromatography coupled with multi-angle l
128                                              Gel-permeation chromatography demonstrated that the [alp
129                           The method employs gel-permeation chromatography fractionation of cell wall
130                                              Gel-permeation chromatography revealed a uniform distrib
131                             Size analysis by gel-permeation chromatography showed CL-L1 in serum to e
132                                              Gel-permeation chromatography showed that the molecular
133                                              Gel-permeation chromatography with quaternary detection
134 utions and molecular forms (as determined by gel-permeation chromatography) of many python GI peptide
135 firmed by a combination of NMR spectroscopy, gel-permeation chromatography, and MALDI-TOF MS.
136 tion in guanidine buffer, buffer exchange by gel-permeation chromatography, and overnight PGAP digest
137                                              Gel-permeation chromatography, dynamic and static light
138 d for the protein-phosphatase activity using gel-permeation chromatography, indicating that the strom
139 nging from 35 to 570 kg/mol as determined by gel-permeation chromatography, was quantitatively correl
140  by quantification of the released PEG using gel-permeation chromatography.
141 debranched starch fractions were analyzed by gel-permeation chromatography.
142 zed by (1) H and (13) C NMR spectroscopy and gel-permeation chromatography.
143  and some small rings have been separated by gel-permeation chromatography.
144 in water-soluble fractions were separated by gel-permeation chromatography.
145        The analytical technique was based on gel-permeation-chromatography with quadruple detection s
146 urified by aqueous two- phase extraction and gel permeation column chromatography, and used as a redu
147  ISA1 to be a dimer, in contrast to previous gel permeation data that estimated the molecular mass as
148 ing formation of small oligomers detected by gel permeation high-performance liquid chromatography, t
149 All cultivars were characterized by RP-HPLC, gel permeation HPLC and R5 and G12 ELISA.
150                                              Gel permeation HPLC of the un-polymerized fractions reve
151                                              Gel permeation HPLC showed that the beta-CN hydrolysate
152 tilage, followed by sequential ion-exchange, gel permeation, hydrophobic, and Zn2+ chelate chromatogr
153 peptides could be completely separated using gel permeation in the presence of sodium dodecyl sulfate
154  of E(#) with the hydrophobic patches on the gel-permeation matrix.
155                                              Gel permeation of the TMA-MT fraction demonstrated that
156                                              Gel permeation on high-performance liquid chromatography
157 t molecular mass of 59 kDa was obtained from gel permeation studies.

 
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