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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 ents with laser diffraction spectroscopy and gel permeation chromatography.
5 um albumin, ion exchange chromatography, and gel permeation chromatography.
6 tes were determined by mass spectrometry and gel permeation chromatography.
7 Synthesized polymers were analyzed by gel permeation chromatography.
8 s of all four proteins were also detected by gel permeation chromatography.
9 e manufacturers' reported values obtained by gel permeation chromatography.
10 with manufacturers' values as determined by gel permeation chromatography.
11 heir hydrodynamic properties as evidenced by gel permeation chromatography.
12 polydispersity index of 1.2 as determined by gel permeation chromatography.
13 ngle-walled carbon nanotubes (s-SWNTs) using gel permeation chromatography.
14 itated with ethanol, and further purified by gel permeation chromatography.
15 debranched starch fractions were analyzed by gel-permeation chromatography.
16 and some small rings have been separated by gel-permeation chromatography.
17 in water-soluble fractions were separated by gel-permeation chromatography.
18 by quantification of the released PEG using gel-permeation chromatography.
19 cyclic polymer product was characterized by gel permeation chromatography, (1)H NMR spectroscopy, an
20 partition coefficient (K(av)) measured with gel permeation chromatography, a high hydrodynamic radiu
21 d wild-type mice were analyzed by sequential gel permeation chromatography/acid-urea polyacrylamide g
22 g electron microscopy, pharmacokinetics, and gel permeation chromatography analyses at various time p
25 bind melittin was assessed using analytical gel permeation chromatography, analytical ultracentrifug
26 ed a panel of biophysical methods, including gel permeation chromatography, analytical ultracentrifug
28 accharides were purified by using Bio-Gel P4 gel permeation chromatography and characterized by nucle
31 as DNA separation matrixes were measured by gel permeation chromatography and multiangle laser light
33 igh molecular mass ISA complexes resolved by gel permeation chromatography and native-polyacrylamide
34 discrete size (<4 x 10(6) Da) as measured by gel permeation chromatography and remain intact after di
36 Six young red wines were fractionated by gel permeation chromatography and subsequently each frac
37 action products isolated from barley malt by gel permeation chromatography and ultrafiltration on the
38 ent molecular mass of 600 kDa as measured by gel permeation chromatography and, like the membranes of
39 lar weight distributions, as demonstrated by gel-permeation chromatography and (1)H NMR spectroscopy.
40 ecipitation, ammonium sulfate precipitation, gel-permeation chromatography and concanavalin-A-Sepharo
41 The same process is further characterized by gel-permeation chromatography and fluorescence resonance
42 s synthesized and characterized by (1)H NMR, gel permeation chromatography, and differential scanning
43 domains by circular dichroism spectroscopy, gel permeation chromatography, and intrinsic viscosity d
44 lly characterized using 1H NMR spectroscopy, gel permeation chromatography, and oligosaccharide profi
47 tion in guanidine buffer, buffer exchange by gel-permeation chromatography, and overnight PGAP digest
50 desorption/ionization mass spectrometry and gel permeation chromatography, confirming successful mol
52 ss of the APPL by over 50%, as determined by gel-permeation chromatography coupled with multi-angle l
55 n reaction products using immunoblotting and gel permeation chromatography demonstrated that PC2 can
58 ar weight distributions similar to those for gel permeation chromatography for polyethylene polymers,
59 clear magnetic resonance characterization of gel permeation chromatography-fractionated acetylated ma
62 The final cleanup procedure consisted of (i) gel permeation chromatography (GPC) and adsorption chrom
63 y (1)H NMR and UV absorption spectroscopies, gel permeation chromatography (GPC) and light scattering
65 r of primary amino groups were determined by gel permeation chromatography (GPC) and potentiometric t
66 tracted with ethyl acetate and purified with gel permeation chromatography (GPC) and primary/secondar
67 [4+2] cycloaddition reaction, as observed by gel permeation chromatography (GPC) and UV-vis spectrosc
68 in, we have developed a simple and versatile gel permeation chromatography (GPC) methodology for mole
69 d the polydispersity index was determined by gel permeation chromatography (GPC) to be as low as 1.34
70 of-flight mass spectrometry (ESI-TOF MS) and gel permeation chromatography (GPC) were used to study t
77 a, SSIII, BEIIa, and BEIIb all comigrated in gel permeation chromatography in a high molecular mass f
80 d for the protein-phosphatase activity using gel-permeation chromatography, indicating that the strom
81 th FeSO4, phenylalanine, and DTT followed by gel permeation chromatography leads to an iron-hydroxyla
82 tely C6H11SiH3 approximately C8H15SiH3, with gel permeation chromatography-multi-angle laser light sc
83 molecular weights were determined by tandem gel permeation chromatography-multiangle laser light sca
86 lation with either DMS or MMPA coeluted upon gel permeation chromatography of extracts of acetate-gro
89 rom wild-type L-FABP (+/+) mice, isolated by gel permeation chromatography of liver soluble proteins,
92 utions and molecular forms (as determined by gel-permeation chromatography) of many python GI peptide
93 I peptide hydrolysate was fractionated using gel permeation chromatography, OFFGEL isoelectric focusi
94 olymers and DNA by means of electrophoresis, gel permeation chromatography or filtration exploits siz
95 rial properties and is generally analyzed by gel permeation chromatography or more recently, by MALDI
96 ysis of purified preparations of FBS AChE by gel permeation chromatography revealed the presence of a
98 and alphaA-R116C-crystallin were studied by gel permeation chromatography, SDS-polyacrylamide gel el
99 tering measurements on proteins separated by gel permeation chromatography showed a small amount of h
106 tron paramagnetic resonance spectroscopy and gel permeation chromatography under a variety of experim
108 tron paramagnetic resonance spectroscopy and gel permeation chromatography were employed to study the
110 cular weight of 91 kDa that co-eluted during gel permeation chromatography with plastidial CT and ACC
111 A combination of lectin, anion exchange, and gel permeation chromatography yielded milligram quantiti
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