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1 ot deoxygenated alpha-cpbeta was observed by gel chromatography.
2 ys, fluorescence anisotropy measurements and gel chromatography.
3  showed a tetrameric subunit organization by gel chromatography.
4 this activity was further enriched by silica 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 38 spots of protein were discovered using 2D gel chromatography.
10  those obtained by RIA and immunoassay after gel chromatography.
11  an intramolecular cyclization during silica gel chromatography, affording a thiazolidinium salt.
12                                              Gel chromatography analysis indicated that aggrecan was
13                                              Gel chromatography analysis of blood samples revealed th
14 bsolute basis by a combination of calibrated gel chromatography and absolute ultracentrifugation tech
15 nts extracts were purified by Sephadex LH-20 gel chromatography and analyzed by UPLC-ESI-MS/MS.
16  domain was monomeric both by size exclusion gel chromatography and by sodium dodecyl sulfate polyacr
17 ates are stable to air, moisture, and silica gel chromatography and can be easily handled without any
18 rate derivatives that are purified by silica gel chromatography and converted to the desired compound
19 leoside triphosphates are purified by silica gel chromatography and converted to their desired compou
20 hese model compounds are separable by silica gel chromatography and readily form single crystals.
21 l allylboronates could be purified by silica gel chromatography and stored in the freezer without dec
22                                   Analytical gel chromatography and ultracentrifugation indicated tet
23 sis, isolation, purification (routine silica gel chromatography), and spectroscopic characterization
24 t through ammonium sulfate precipitation and gel chromatography, and identified by N-terminal sequenc
25 ll proportion runs with a size of <15 kDa by gel chromatography; and 4) native PAGE of AF yields a ba
26 these maize cultivars was tested by affinity gel chromatography followed by sodium dodecyl sulfate-po
27 lution of decorin protein core in Superose 6 gel chromatography gave masses compatible with monomeric
28 cal ultracentrifuge combined with calibrated gel chromatography give a molecular mass M of (77 +/- 4)
29              The complex is stable to silica gel chromatography (hexanes/ethyl acetate), dilute triet
30 thesized glycosaminoglycans were measured by gel chromatography, high performance liquid chromatograp
31                               Size exclusion gel chromatography in the spin column format provides th
32 -stable and can be easily purified by silica gel chromatography; in contrast, secondary allylboronate
33 nes the inherent strengths of size exclusion gel chromatography, mass spectrometry, and NMR to identi
34                                              Gel chromatography of biles (TC/(TC + EYPC) = 0.7) ultra
35  It was isolated as a complex with fibrin by gel chromatography of cryoprecipitates and then separate
36                                   Analytical gel chromatography of mouse NAGS (mNAGS) indicated eithe
37 h high purities affordable via simple silica gel chromatography only.
38                                  However, by gel chromatography, only 19 percent +/- 2 percent (Ch/EY
39 erum without additional manipulations (e.g., gel chromatography or PEG-precipitation).
40                         This was assessed by gel chromatography, SDS-polyacrylamide gel electrophores
41  of ligation has been explored by analytical gel chromatography, sedimentation equilibrium, and oxyge
42                               Size-exclusion gel chromatography showed that the monomeric and dimeric
43 -soluble amyloid, purified by size-exclusion gel chromatography, showed that Abeta 1-40 and its carbo
44                                              Gel chromatography studies further support the formation
45 ncluding low pH aqueous solutions and silica gel chromatography; the di-tert-butylfluorosilyl ethers
46 in the series, was measured using analytical gel chromatography to be 9 kcal/tetramer less favorable
47                             As compared with gel chromatography, ultracentrifugation systematically e
48 to 31 percent, thus approaching the initial (gel chromatography) value.
49                                              Gel chromatography was performed using eluants containin
50 -)(9)-10(-)(3) M using large-zone analytical gel chromatography with radiolabeled repressor.
51 gation can alter the phases present in bile, gel chromatography with the correct IMC more accurately
52      Identical model biles were subjected to gel chromatography with the correct IMC, either directly
53 ithogenic bile, both ultracentrifugation and gel chromatography with the correct intermixed micellar/