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1 ion as a hybrid form of conventional HIC and reverse phase chromatography.
2 gained when analyzing the glycans by online reverse phase chromatography.
3 spectrometry (HPLC-MS) using both normal and reverse phase chromatography.
4 ents remain soluble, that is compatible with reverse phase chromatography.
5 olution of the nucleic acids during ion pair reverse phase chromatography.
6 d, high-resolution separation using ion pair reverse phase chromatography.
7 -Sepharose affinity, gel filtration, and C18 reverse-phase chromatography.
8 d by sequential kallikrein-Sepharose and C18 reverse-phase chromatography.
9 Three active components were also found by reverse-phase chromatography.
10 from [(3)H]glibenclamide-injected animals by reverse-phase chromatography.
11 ventional hydrophobic separations such as in reverse-phase chromatography.
12 on-exchange perfusion chromatography, and C4 reverse-phase chromatography.
13 urified by size exclusion chromatography and reversed phase chromatography.
14 e partial separation of oxidation isomers by reversed phase chromatography.
15 fied from yeast media by cation-exchange and reversed phase chromatography.
16 sed-phase material for on-chip desalting and reversed-phase chromatography.
17 l detector was developed in hyphenation with reversed-phase chromatography.
18 eric ether lipid pairs can be separated with reversed-phase chromatography.
19 actionated by off-gel isoelectrofocusing and reversed-phase chromatography.
20 d with both alkylation reagents, coeluted on reversed-phase chromatography.
21 ution of heavy isotope coded peptides during reversed-phase chromatography.
22 ping and their subunit content determined by reversed-phase chromatography.
23 similar to those of typical ODS packings for reversed-phase chromatography.
24 rified from both sources by ion-exchange and reversed-phase chromatographies.
27 e resulting phosphopeptides were isolated by reverse phase chromatography and directly identified by
28 tabolomics approach beginning with capillary reverse phase chromatography and electrospray ionization
29 d aniline-tagged glycans can be recovered by reverse-phase chromatography and can be quantified based
30 duced cleavage products were monitored using reverse-phase chromatography and matrix-assisted laser d
32 by ultrafiltration followed by low-pressure reverse-phase chromatography and purified by reverse-pha
33 y ionizable or retained analytes amenable to reversed phase chromatography and electrospray ionizatio
34 es (aqueous extract) combined with HILIC and reversed phase chromatography and time-of-flight mass sp
36 cosylated sample was further fractionated by reversed-phase chromatography and analyzed by electrospr
37 the same amino acid sequence are resolved by reversed-phase chromatography and assesses the degree to
38 /MS/MS with strong cation exchange (SCX) and reversed-phase chromatography and continuous gradient el
40 -alkylnicotinic acid (Cn-NA-NHS) followed by reversed-phase chromatography and electrospray ionizatio
41 e mixture was analyzed by single-dimensional reversed-phase chromatography and electrospray ionizatio
42 es were isolated using cationic exchange and reversed-phase chromatography and identified by (1)H NMR
44 stion of these oxidized proteins followed by reversed-phase chromatography and tandem mass spectromet
46 ones in culture supernatants fractionated by reverse-phase chromatography, and mass spectrometry was
47 molecules are resolved by using ion-pairing reverse-phase chromatography, and their exact masses are
48 eterodimer using gel filtration, amino acid, reversed-phase chromatography, and analytical ultracentr
49 erivatized individually, mixed, subjected to reversed-phase chromatography, and analyzed by ESI-MS.
50 AH was separated using ultra-filtration and reversed-phase chromatography, and assessment of the fra
51 scent assay components are then separated by reversed-phase chromatography, and NBD-serine is quantif
52 ractionation of deglycosylated peptides with reversed-phase chromatography, and peptide sequencing wi
53 hickens were separated by gel filtration and reversed-phase chromatography, and whole protein masses
55 g separation techniques for LC-IRMS, such as reversed phase chromatography at normal temperatures, io
56 ample preparation, off-line fractionation by reversed-phase chromatography at pH 10, immobilization o
57 lected proteins were further fractionated by reversed-phase chromatography before proteolysis of indi
59 analytical microbore and capillary perfusion reversed-phase chromatography columns are analyzed by ei
60 esting times were analyzed using ion-pairing reversed-phase chromatography coupled to an ICPMS/MS det
61 mino acid analysis as well as microcapillary reverse phase chromatography electrospray ionization tan
63 philic interaction liquid chromatography and reversed-phase chromatography enables the investigation
65 collected, pooled together and subjected to reversed-phase chromatography for further purification.
67 e to separate the isomers, or who were using reversed-phase chromatography, gave rise to multi-modal
68 Due to the hydrophilic nature of glycans, reverse phase chromatography has not been widely used as
69 matography using the sequential ion-exchange/reversed-phase chromatography HPLC system, and detection
70 labeled LaeA followed by cation exchange and reverse phase chromatography identified methionine as th
71 in both identity as well as purity, ion-pair reversed-phase chromatography (IP-RP) at high temperatur
72 ize exclusion chromatography (SEC), ion-pair reversed phase chromatography (IPRP), and hydrophilic in
74 ass of cationic ion-interaction reagents for reversed-phase chromatography is introduced in the prese
76 med by an immobilized trypsin cartridge, and reversed-phase chromatography isolates the two pools of
77 niques, including cyanogen bromide cleavage, reversed-phase chromatography, mass spectrometry, and N-
78 (salt-free) ion exchange chromatography and reversed phase chromatography-mass spectrometry allowed
82 ate free energies of adsorption from data on reversed-phase chromatography on nine protected peptides
83 oxylic acid cycle (TCA cycle), by mixed-mode reversed-phase chromatography, on a CSH Phenyl-Hexyl col
84 y involves denaturing methodologies, such as reversed-phase chromatography or capillary electrophores
88 e (SMRT) dataset, an experimentally acquired reverse-phase chromatography retention time dataset cove
91 (ACE) in the first separation dimension and reversed phase chromatography (RP) in the second separat
92 sSEC fractions could be further separated by reverse phase chromatography (RPC) coupled online with h
93 C with ion exchange chromatography (IEC) and reverse phase chromatography (RPC) for intact protein se
96 m interacting with the stationary phase of a reversed-phase chromatography (RPC) column and impacting
97 graphy seleno-amino acids were determined by reversed-phase chromatography (RPC) coupled to ICP-MS.
98 rial size exclusion chromatography (sSEC) to reversed-phase chromatography (RPC) expanded coverage of
99 tides increased retention of peptides during reversed-phase chromatography (RPC), particularly in the
101 rs to develop a highly selective ion-pairing reversed-phase chromatography separation for sgRNAs.
103 eparation of derivatized N-linked glycans by reverse phase chromatography significantly out-performs
104 lysis of these newly discovered congeners by reverse-phase chromatography, spectrophotometry, antibod
105 d on the retention time derived from routine reverse-phase chromatography tandem mass spectrometry (R
106 techniques and peptide retention modeling in reversed-phase chromatography to generate a data set suf
107 rst dimension are automatically subjected to reversed-phase chromatography to separate similarly size
108 NA derivatized amino acids was lengthened in reversed-phase chromatography to the extent that polar a
109 ms using high pressure liquid chromatography-reverse phase chromatography together with synthetic pep
110 d through a combination of methods including reversed-phase chromatography, treatment with phosphatid
111 luorescent assay components are separated by reversed-phase chromatography under isocratic conditions
112 extracts of apple peels were fractionated by reversed phase chromatography using gradient elution of
113 ethanesulfonate, (3) sequential ion-exchange/reversed-phase chromatography using a single non-end-cap
114 14 to 36 carbon atoms are separated by C(8) reversed-phase chromatography using a water-methanol gra
115 (microcon filtration, molecular sieving, and reversed-phase chromatography), we unambiguously identif
116 se we were unable to resolve the isoforms by reverse phase chromatography, we could not assign each i
117 etylation resulted in increased retention in reversed-phase chromatography, whereas methylation, incl
119 peptides, can be challenging to separate by reverse-phase chromatography with optimal efficiency.
120 hylls and bacteriochlorophylls) was based on reversed-phase chromatography with a methanol-acetone gr
121 profiled by untargeted metabolomics, namely, reversed-phase chromatography with negative electrospray
122 tract of Maieta guianensis by silica gel and reverse-phase chromatography yielded two pure compounds