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1 vity co-purifies with ACCase activity during gel permeation chromatography.
2 ntly associated dimer during ion-exchange or gel permeation chromatography.
3 sacylase activity are partially separated by gel permeation chromatography.
4 aponified and the bulky PC-8 was enriched by gel permeation chromatography.
5 ents with laser diffraction spectroscopy and gel permeation chromatography.
6 um albumin, ion exchange chromatography, and gel permeation chromatography.
7 tes were determined by mass spectrometry and gel permeation chromatography.
8 Synthesized polymers were analyzed by gel permeation chromatography.
9 s of all four proteins were also detected by gel permeation chromatography.
10 e manufacturers' reported values obtained by gel permeation chromatography.
11 with manufacturers' values as determined by gel permeation chromatography.
12 heir hydrodynamic properties as evidenced by gel permeation chromatography.
13 polydispersity index of 1.2 as determined by gel permeation chromatography.
14 ngle-walled carbon nanotubes (s-SWNTs) using gel permeation chromatography.
15 itated with ethanol, and further purified by gel permeation chromatography.
16 by quantification of the released PEG using gel-permeation chromatography.
17 debranched starch fractions were analyzed by gel-permeation chromatography.
18 zed by (1) H and (13) C NMR spectroscopy and gel-permeation chromatography.
19 and some small rings have been separated by gel-permeation chromatography.
20 in water-soluble fractions were separated by gel-permeation chromatography.
21 cyclic polymer product was characterized by gel permeation chromatography, (1)H NMR spectroscopy, an
22 partition coefficient (K(av)) measured with gel permeation chromatography, a high hydrodynamic radiu
23 d wild-type mice were analyzed by sequential gel permeation chromatography/acid-urea polyacrylamide g
24 g electron microscopy, pharmacokinetics, and gel permeation chromatography analyses at various time p
27 ed a panel of biophysical methods, including gel permeation chromatography, analytical ultracentrifug
28 bind melittin was assessed using analytical gel permeation chromatography, analytical ultracentrifug
30 accharides were purified by using Bio-Gel P4 gel permeation chromatography and characterized by nucle
34 as DNA separation matrixes were measured by gel permeation chromatography and multiangle laser light
36 igh molecular mass ISA complexes resolved by gel permeation chromatography and native-polyacrylamide
37 discrete size (<4 x 10(6) Da) as measured by gel permeation chromatography and remain intact after di
39 Six young red wines were fractionated by gel permeation chromatography and subsequently each frac
40 action products isolated from barley malt by gel permeation chromatography and ultrafiltration on the
41 ent molecular mass of 600 kDa as measured by gel permeation chromatography and, like the membranes of
42 lar weight distributions, as demonstrated by gel-permeation chromatography and (1)H NMR spectroscopy.
43 ecipitation, ammonium sulfate precipitation, gel-permeation chromatography and concanavalin-A-Sepharo
44 The same process is further characterized by gel-permeation chromatography and fluorescence resonance
45 whole cell-wall nuclear magnetic resonance, gel-permeation chromatography and transcriptome sequenci
46 alyzed using X-ray microcomputed tomography, gel permeation chromatography, and (1)H-nuclear magnetic
47 s synthesized and characterized by (1)H NMR, gel permeation chromatography, and differential scanning
48 domains by circular dichroism spectroscopy, gel permeation chromatography, and intrinsic viscosity d
49 lly characterized using 1H NMR spectroscopy, gel permeation chromatography, and oligosaccharide profi
52 tion in guanidine buffer, buffer exchange by gel-permeation chromatography, and overnight PGAP digest
55 desorption/ionization mass spectrometry and gel permeation chromatography, confirming successful mol
57 ss of the APPL by over 50%, as determined by gel-permeation chromatography coupled with multi-angle l
61 n reaction products using immunoblotting and gel permeation chromatography demonstrated that PC2 can
65 ar weight distributions similar to those for gel permeation chromatography for polyethylene polymers,
66 clear magnetic resonance characterization of gel permeation chromatography-fractionated acetylated ma
70 The final cleanup procedure consisted of (i) gel permeation chromatography (GPC) and adsorption chrom
71 y (1)H NMR and UV absorption spectroscopies, gel permeation chromatography (GPC) and light scattering
73 r of primary amino groups were determined by gel permeation chromatography (GPC) and potentiometric t
74 tracted with ethyl acetate and purified with gel permeation chromatography (GPC) and primary/secondar
75 ess-strain mechanical measurement, (1)H NMR, gel permeation chromatography (GPC) and thermogravimetri
76 [4+2] cycloaddition reaction, as observed by gel permeation chromatography (GPC) and UV-vis spectrosc
77 on rely on measuring the molecular weight by gel permeation chromatography (GPC) based on polystyrene
78 alytical parameter in polymer analysis, with gel permeation chromatography (GPC) being the most commo
80 in, we have developed a simple and versatile gel permeation chromatography (GPC) methodology for mole
81 confirm more than 99 % DMAC conversion while gel permeation chromatography (GPC) studies indicate wel
82 d the polydispersity index was determined by gel permeation chromatography (GPC) to be as low as 1.34
83 of-flight mass spectrometry (ESI-TOF MS) and gel permeation chromatography (GPC) were used to study t
84 ze challenging 2D-LC workflows: (1) coupling gel permeation chromatography (GPC) with reversed-phase
87 R) spectroscopy, infrared (IR) spectroscopy, gel permeation chromatography (GPC), and high-resolution
88 om polyolefin separation techniques, such as gel permeation chromatography (GPC), crystallization elu
89 on of the polymer cyclic topology comes from gel permeation chromatography (GPC), dynamic light scatt
90 gh-Performance Liquid Chromatography (HPLC), Gel permeation chromatography (GPC), Fourier Transform I
91 e primary tool used to determine plastic MW, gel permeation chromatography (GPC), has major limitatio
92 -NIR absorption/fluorescence spectroscopies, gel permeation chromatography (GPC), NMR, and DFT simula
93 The degradation process was monitored by gel permeation chromatography (GPC), scanning electron m
94 rstanding of the bias-inducing mechanisms in gel permeation chromatography (GPC), the magnitude of er
100 a, SSIII, BEIIa, and BEIIb all comigrated in gel permeation chromatography in a high molecular mass f
103 d for the protein-phosphatase activity using gel-permeation chromatography, indicating that the strom
104 th FeSO4, phenylalanine, and DTT followed by gel permeation chromatography leads to an iron-hydroxyla
105 tely C6H11SiH3 approximately C8H15SiH3, with gel permeation chromatography-multi-angle laser light sc
106 molecular weights were determined by tandem gel permeation chromatography-multiangle laser light sca
109 tron-paramagnetic resonance spectroscopy and gel permeation chromatography of cryomilled samples, in
110 lation with either DMS or MMPA coeluted upon gel permeation chromatography of extracts of acetate-gro
113 rom wild-type L-FABP (+/+) mice, isolated by gel permeation chromatography of liver soluble proteins,
114 by nuclear magnetic resonance spectroscopy, gel permeation chromatography of polymers extracted from
117 utions and molecular forms (as determined by gel-permeation chromatography) of many python GI peptide
118 I peptide hydrolysate was fractionated using gel permeation chromatography, OFFGEL isoelectric focusi
119 olymers and DNA by means of electrophoresis, gel permeation chromatography or filtration exploits siz
120 rial properties and is generally analyzed by gel permeation chromatography or more recently, by MALDI
121 ysis of purified preparations of FBS AChE by gel permeation chromatography revealed the presence of a
123 and alphaA-R116C-crystallin were studied by gel permeation chromatography, SDS-polyacrylamide gel el
124 tering measurements on proteins separated by gel permeation chromatography showed a small amount of h
131 tron paramagnetic resonance spectroscopy and gel permeation chromatography under a variety of experim
134 nging from 35 to 570 kg/mol as determined by gel-permeation chromatography, was quantitatively correl
135 tron paramagnetic resonance spectroscopy and gel permeation chromatography were employed to study the
136 esonance spectroscopy, X-ray diffraction and gel permeation chromatography were used to monitor the c
138 cular weight of 91 kDa that co-eluted during gel permeation chromatography with plastidial CT and ACC
141 A combination of lectin, anion exchange, and gel permeation chromatography yielded milligram quantiti