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1 gained when analyzing the glycans by online reverse phase chromatography.
2 spectrometry (HPLC-MS) using both normal and reverse phase chromatography.
3 ents remain soluble, that is compatible with reverse phase chromatography.
4 olution of the nucleic acids during ion pair reverse phase chromatography.
5 d, high-resolution separation using ion pair reverse phase chromatography.
6 ion as a hybrid form of conventional HIC and reverse phase chromatography.
7 Three active components were also found by reverse-phase chromatography.
8 from [(3)H]glibenclamide-injected animals by reverse-phase chromatography.
9 ventional hydrophobic separations such as in reverse-phase chromatography.
10 on-exchange perfusion chromatography, and C4 reverse-phase chromatography.
11 -Sepharose affinity, gel filtration, and C18 reverse-phase chromatography.
12 d by sequential kallikrein-Sepharose and C18 reverse-phase chromatography.
13 fied from yeast media by cation-exchange and reversed phase chromatography.
14 urified by size exclusion chromatography and reversed phase chromatography.
15 actionated by off-gel isoelectrofocusing and reversed-phase chromatography.
16 d with both alkylation reagents, coeluted on reversed-phase chromatography.
17 ution of heavy isotope coded peptides during reversed-phase chromatography.
18 ping and their subunit content determined by reversed-phase chromatography.
19 similar to those of typical ODS packings for reversed-phase chromatography.
20 rified from both sources by ion-exchange and reversed-phase chromatographies.
23 e resulting phosphopeptides were isolated by reverse phase chromatography and directly identified by
24 tabolomics approach beginning with capillary reverse phase chromatography and electrospray ionization
25 d aniline-tagged glycans can be recovered by reverse-phase chromatography and can be quantified based
26 duced cleavage products were monitored using reverse-phase chromatography and matrix-assisted laser d
27 by ultrafiltration followed by low-pressure reverse-phase chromatography and purified by reverse-pha
28 y ionizable or retained analytes amenable to reversed phase chromatography and electrospray ionizatio
30 cosylated sample was further fractionated by reversed-phase chromatography and analyzed by electrospr
31 the same amino acid sequence are resolved by reversed-phase chromatography and assesses the degree to
32 /MS/MS with strong cation exchange (SCX) and reversed-phase chromatography and continuous gradient el
34 -alkylnicotinic acid (Cn-NA-NHS) followed by reversed-phase chromatography and electrospray ionizatio
35 e mixture was analyzed by single-dimensional reversed-phase chromatography and electrospray ionizatio
36 es were isolated using cationic exchange and reversed-phase chromatography and identified by (1)H NMR
38 stion of these oxidized proteins followed by reversed-phase chromatography and tandem mass spectromet
40 ones in culture supernatants fractionated by reverse-phase chromatography, and mass spectrometry was
41 eterodimer using gel filtration, amino acid, reversed-phase chromatography, and analytical ultracentr
42 erivatized individually, mixed, subjected to reversed-phase chromatography, and analyzed by ESI-MS.
43 AH was separated using ultra-filtration and reversed-phase chromatography, and assessment of the fra
44 scent assay components are then separated by reversed-phase chromatography, and NBD-serine is quantif
45 ractionation of deglycosylated peptides with reversed-phase chromatography, and peptide sequencing wi
46 hickens were separated by gel filtration and reversed-phase chromatography, and whole protein masses
48 g separation techniques for LC-IRMS, such as reversed phase chromatography at normal temperatures, io
49 ample preparation, off-line fractionation by reversed-phase chromatography at pH 10, immobilization o
50 lected proteins were further fractionated by reversed-phase chromatography before proteolysis of indi
52 analytical microbore and capillary perfusion reversed-phase chromatography columns are analyzed by ei
53 mino acid analysis as well as microcapillary reverse phase chromatography electrospray ionization tan
56 collected, pooled together and subjected to reversed-phase chromatography for further purification.
58 e to separate the isomers, or who were using reversed-phase chromatography, gave rise to multi-modal
59 Due to the hydrophilic nature of glycans, reverse phase chromatography has not been widely used as
60 matography using the sequential ion-exchange/reversed-phase chromatography HPLC system, and detection
61 labeled LaeA followed by cation exchange and reverse phase chromatography identified methionine as th
64 med by an immobilized trypsin cartridge, and reversed-phase chromatography isolates the two pools of
65 niques, including cyanogen bromide cleavage, reversed-phase chromatography, mass spectrometry, and N-
66 (salt-free) ion exchange chromatography and reversed phase chromatography-mass spectrometry allowed
70 ate free energies of adsorption from data on reversed-phase chromatography on nine protected peptides
76 (ACE) in the first separation dimension and reversed phase chromatography (RP) in the second separat
77 sSEC fractions could be further separated by reverse phase chromatography (RPC) coupled online with h
78 C with ion exchange chromatography (IEC) and reverse phase chromatography (RPC) for intact protein se
81 m interacting with the stationary phase of a reversed-phase chromatography (RPC) column and impacting
82 graphy seleno-amino acids were determined by reversed-phase chromatography (RPC) coupled to ICP-MS.
83 tides increased retention of peptides during reversed-phase chromatography (RPC), particularly in the
86 eparation of derivatized N-linked glycans by reverse phase chromatography significantly out-performs
87 lysis of these newly discovered congeners by reverse-phase chromatography, spectrophotometry, antibod
88 techniques and peptide retention modeling in reversed-phase chromatography to generate a data set suf
89 rst dimension are automatically subjected to reversed-phase chromatography to separate similarly size
90 NA derivatized amino acids was lengthened in reversed-phase chromatography to the extent that polar a
91 ms using high pressure liquid chromatography-reverse phase chromatography together with synthetic pep
92 d through a combination of methods including reversed-phase chromatography, treatment with phosphatid
93 luorescent assay components are separated by reversed-phase chromatography under isocratic conditions
94 extracts of apple peels were fractionated by reversed phase chromatography using gradient elution of
95 ethanesulfonate, (3) sequential ion-exchange/reversed-phase chromatography using a single non-end-cap
96 14 to 36 carbon atoms are separated by C(8) reversed-phase chromatography using a water-methanol gra
97 (microcon filtration, molecular sieving, and reversed-phase chromatography), we unambiguously identif
98 se we were unable to resolve the isoforms by reverse phase chromatography, we could not assign each i
99 etylation resulted in increased retention in reversed-phase chromatography, whereas methylation, incl
100 peptides, can be challenging to separate by reverse-phase chromatography with optimal efficiency.
101 tract of Maieta guianensis by silica gel and reverse-phase chromatography yielded two pure compounds
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