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1 this activity was further enriched by silica gel chromatography.
2 ot deoxygenated alpha-cpbeta was observed by gel chromatography.
3 ys, fluorescence anisotropy measurements and gel chromatography.
4 showed a tetrameric subunit organization by gel chromatography.
5 mass range 10 to 100 kDa was fractionated by gel chromatography.
6 amic changes using high-precision analytical gel chromatography.
7 (PGs) were analyzed using Sephacryl S-500 HR gel chromatography.
8 rified by ammonium sulfate precipitation and gel chromatography.
9 those obtained by RIA and immunoassay after gel chromatography.
12 bsolute basis by a combination of calibrated gel chromatography and absolute ultracentrifugation tech
13 domain was monomeric both by size exclusion gel chromatography and by sodium dodecyl sulfate polyacr
14 ates are stable to air, moisture, and silica gel chromatography and can be easily handled without any
15 hese model compounds are separable by silica gel chromatography and readily form single crystals.
16 l allylboronates could be purified by silica gel chromatography and stored in the freezer without dec
18 sis, isolation, purification (routine silica gel chromatography), and spectroscopic characterization
19 t through ammonium sulfate precipitation and gel chromatography, and identified by N-terminal sequenc
20 ll proportion runs with a size of <15 kDa by gel chromatography; and 4) native PAGE of AF yields a ba
21 these maize cultivars was tested by affinity gel chromatography followed by sodium dodecyl sulfate-po
22 lution of decorin protein core in Superose 6 gel chromatography gave masses compatible with monomeric
23 cal ultracentrifuge combined with calibrated gel chromatography give a molecular mass M of (77 +/- 4)
25 thesized glycosaminoglycans were measured by gel chromatography, high performance liquid chromatograp
27 -stable and can be easily purified by silica gel chromatography; in contrast, secondary allylboronate
28 nes the inherent strengths of size exclusion gel chromatography, mass spectrometry, and NMR to identi
30 It was isolated as a complex with fibrin by gel chromatography of cryoprecipitates and then separate
35 of ligation has been explored by analytical gel chromatography, sedimentation equilibrium, and oxyge
37 -soluble amyloid, purified by size-exclusion gel chromatography, showed that Abeta 1-40 and its carbo
39 ncluding low pH aqueous solutions and silica gel chromatography; the di-tert-butylfluorosilyl ethers
40 in the series, was measured using analytical gel chromatography to be 9 kcal/tetramer less favorable
45 gation can alter the phases present in bile, gel chromatography with the correct IMC more accurately
47 ithogenic bile, both ultracentrifugation and gel chromatography with the correct intermixed micellar/
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