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1 imental conditions examined as determined by gel permeation and sedimentation equilibrium analysis.
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
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 [4+2] cycloaddition reaction, as observed by gel permeation chromatography (GPC) and UV-vis spectrosc
13 in, we have developed a simple and versatile gel permeation chromatography (GPC) methodology for mole
14 d the polydispersity index was determined by gel permeation chromatography (GPC) to be as low as 1.34
15 of-flight mass spectrometry (ESI-TOF MS) and gel permeation chromatography (GPC) were used to study t
20 g electron microscopy, pharmacokinetics, and gel permeation chromatography analyses at various time p
24 accharides were purified by using Bio-Gel P4 gel permeation chromatography and characterized by nucle
27 as DNA separation matrixes were measured by gel permeation chromatography and multiangle laser light
29 igh molecular mass ISA complexes resolved by gel permeation chromatography and native-polyacrylamide
30 discrete size (<4 x 10(6) Da) as measured by gel permeation chromatography and remain intact after di
32 Six young red wines were fractionated by gel permeation chromatography and subsequently each frac
33 action products isolated from barley malt by gel permeation chromatography and ultrafiltration on the
34 ent molecular mass of 600 kDa as measured by gel permeation chromatography and, like the membranes of
40 n reaction products using immunoblotting and gel permeation chromatography demonstrated that PC2 can
41 ar weight distributions similar to those for gel permeation chromatography for polyethylene polymers,
43 a, SSIII, BEIIa, and BEIIb all comigrated in gel permeation chromatography in a high molecular mass f
46 th FeSO4, phenylalanine, and DTT followed by gel permeation chromatography leads to an iron-hydroxyla
48 lation with either DMS or MMPA coeluted upon gel permeation chromatography of extracts of acetate-gro
51 rom wild-type L-FABP (+/+) mice, isolated by gel permeation chromatography of liver soluble proteins,
54 olymers and DNA by means of electrophoresis, gel permeation chromatography or filtration exploits siz
55 rial properties and is generally analyzed by gel permeation chromatography or more recently, by MALDI
56 ysis of purified preparations of FBS AChE by gel permeation chromatography revealed the presence of a
57 tering measurements on proteins separated by gel permeation chromatography showed a small amount of h
61 tron paramagnetic resonance spectroscopy and gel permeation chromatography under a variety of experim
63 tron paramagnetic resonance spectroscopy and gel permeation chromatography were employed to study the
65 cular weight of 91 kDa that co-eluted during gel permeation chromatography with plastidial CT and ACC
66 A combination of lectin, anion exchange, and gel permeation chromatography yielded milligram quantiti
67 cyclic polymer product was characterized by gel permeation chromatography, (1)H NMR spectroscopy, an
68 partition coefficient (K(av)) measured with gel permeation chromatography, a high hydrodynamic radiu
69 bind melittin was assessed using analytical gel permeation chromatography, analytical ultracentrifug
70 ed a panel of biophysical methods, including gel permeation chromatography, analytical ultracentrifug
71 s synthesized and characterized by (1)H NMR, gel permeation chromatography, and differential scanning
72 domains by circular dichroism spectroscopy, gel permeation chromatography, and intrinsic viscosity d
73 lly characterized using 1H NMR spectroscopy, gel permeation chromatography, and oligosaccharide profi
75 desorption/ionization mass spectrometry and gel permeation chromatography, confirming successful mol
77 I peptide hydrolysate was fractionated using gel permeation chromatography, OFFGEL isoelectric focusi
78 and alphaA-R116C-crystallin were studied by gel permeation chromatography, SDS-polyacrylamide gel el
80 clear magnetic resonance characterization of gel permeation chromatography-fractionated acetylated ma
81 tely C6H11SiH3 approximately C8H15SiH3, with gel permeation chromatography-multi-angle laser light sc
82 molecular weights were determined by tandem gel permeation chromatography-multiangle laser light sca
97 d wild-type mice were analyzed by sequential gel permeation chromatography/acid-urea polyacrylamide g
99 lar weight distributions, as demonstrated by gel-permeation chromatography and (1)H NMR spectroscopy.
100 ecipitation, ammonium sulfate precipitation, gel-permeation chromatography and concanavalin-A-Sepharo
101 The same process is further characterized by gel-permeation chromatography and fluorescence resonance
102 ss of the APPL by over 50%, as determined by gel-permeation chromatography coupled with multi-angle l
107 utions and molecular forms (as determined by gel-permeation chromatography) of many python GI peptide
109 tion in guanidine buffer, buffer exchange by gel-permeation chromatography, and overnight PGAP digest
111 d for the protein-phosphatase activity using gel-permeation chromatography, indicating that the strom
116 ISA1 to be a dimer, in contrast to previous gel permeation data that estimated the molecular mass as
117 ing formation of small oligomers detected by gel permeation high-performance liquid chromatography, t
120 tilage, followed by sequential ion-exchange, gel permeation, hydrophobic, and Zn2+ chelate chromatogr
121 peptides could be completely separated using gel permeation in the presence of sodium dodecyl sulfate
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