ライフサイエンスコーパス: reversed-phase chromatography

1 e partial separation of oxidation isomers by reversed phase chromatography.

2 fied from yeast media by cation-exchange and reversed phase chromatography.

3 urified by size exclusion chromatography and reversed phase chromatography.

4 actionated by off-gel isoelectrofocusing and reversed-phase chromatography.

5 d with both alkylation reagents, coeluted on reversed-phase chromatography.

6 ution of heavy isotope coded peptides during reversed-phase chromatography.

7 ping and their subunit content determined by reversed-phase chromatography.

8 similar to those of typical ODS packings for reversed-phase chromatography.

9 sed-phase material for on-chip desalting and reversed-phase chromatography.

10 l detector was developed in hyphenation with reversed-phase chromatography.

11 eric ether lipid pairs can be separated with reversed-phase chromatography.

12 rified from both sources by ion-exchange and reversed-phase chromatographies.

13 On normal- and reversed-phase chromatography, 1 is substantially less p

14 Purification was based on miniature reversed-phase chromatography, a procedure suitable for

15 y ionizable or retained analytes amenable to reversed phase chromatography and electrospray ionizatio

16 es (aqueous extract) combined with HILIC and reversed phase chromatography and time-of-flight mass sp

17 Reversed-phase chromatography and 1-octanol/water partit

18 cosylated sample was further fractionated by reversed-phase chromatography and analyzed by electrospr

19 the same amino acid sequence are resolved by reversed-phase chromatography and assesses the degree to

20 /MS/MS with strong cation exchange (SCX) and reversed-phase chromatography and continuous gradient el

21 Prymnesins were separated by reversed-phase chromatography and detected by positive-m

22 -alkylnicotinic acid (Cn-NA-NHS) followed by reversed-phase chromatography and electrospray ionizatio

23 e mixture was analyzed by single-dimensional reversed-phase chromatography and electrospray ionizatio

24 es were isolated using cationic exchange and reversed-phase chromatography and identified by (1)H NMR

25 Following trypsin cleavage, reversed-phase chromatography and mass spectrometry (MS)

26 stion of these oxidized proteins followed by reversed-phase chromatography and tandem mass spectromet

27 eterodimer using gel filtration, amino acid, reversed-phase chromatography, and analytical ultracentr

28 erivatized individually, mixed, subjected to reversed-phase chromatography, and analyzed by ESI-MS.

29 AH was separated using ultra-filtration and reversed-phase chromatography, and assessment of the fra

30 scent assay components are then separated by reversed-phase chromatography, and NBD-serine is quantif

31 ractionation of deglycosylated peptides with reversed-phase chromatography, and peptide sequencing wi

32 hickens were separated by gel filtration and reversed-phase chromatography, and whole protein masses

33 Ion exchange and high pH reversed phase chromatography are often used for this pu

34 g separation techniques for LC-IRMS, such as reversed phase chromatography at normal temperatures, io

35 ample preparation, off-line fractionation by reversed-phase chromatography at pH 10, immobilization o

36 lected proteins were further fractionated by reversed-phase chromatography before proteolysis of indi

37 Here, we show that nonaqueous reversed-phase chromatography can be coupled to mass-spe

38 analytical microbore and capillary perfusion reversed-phase chromatography columns are analyzed by ei

39 esting times were analyzed using ion-pairing reversed-phase chromatography coupled to an ICPMS/MS det

40 Reversed phase chromatography, electrospray ionization-M

41 philic interaction liquid chromatography and reversed-phase chromatography enables the investigation

42 HPLC-ICP-MS based on ion-paired reversed phase chromatography for the selenium speciatio

43 collected, pooled together and subjected to reversed-phase chromatography for further purification.

44 tography (HILIC) for the aqueous extract and reversed-phase chromatography for the organic.

45 e to separate the isomers, or who were using reversed-phase chromatography, gave rise to multi-modal

46 matography using the sequential ion-exchange/reversed-phase chromatography HPLC system, and detection

47 in both identity as well as purity, ion-pair reversed-phase chromatography (IP-RP) at high temperatur

48 ize exclusion chromatography (SEC), ion-pair reversed phase chromatography (IPRP), and hydrophilic in

49 it is orthogonal to hydrophobicity on which reversed-phase chromatography is based.

50 ass of cationic ion-interaction reagents for reversed-phase chromatography is introduced in the prese

51 ge of the analysis using subzero temperature reversed-phase chromatography is presented.

52 med by an immobilized trypsin cartridge, and reversed-phase chromatography isolates the two pools of

53 niques, including cyanogen bromide cleavage, reversed-phase chromatography, mass spectrometry, and N-

54 (salt-free) ion exchange chromatography and reversed phase chromatography-mass spectrometry allowed

55 noliths (PPMs) that are versatile and robust reversed-phase chromatography media.

56 rst separated from reaction side products by reversed-phase chromatography on a C-4 column.

57 ate free energies of adsorption from data on reversed-phase chromatography on nine protected peptides

58 oxylic acid cycle (TCA cycle), by mixed-mode reversed-phase chromatography, on a CSH Phenyl-Hexyl col

59 y involves denaturing methodologies, such as reversed-phase chromatography or capillary electrophores

60 ation columns were packed using conventional reversed-phase chromatography particles.

61 Reversed-phase chromatography revealed that most SAR11 b

62 (ACE) in the first separation dimension and reversed phase chromatography (RP) in the second separat

63 Using complementary reversed-phase chromatography (RPC) and hydrophilic inte

64 m interacting with the stationary phase of a reversed-phase chromatography (RPC) column and impacting

65 graphy seleno-amino acids were determined by reversed-phase chromatography (RPC) coupled to ICP-MS.

66 rial size exclusion chromatography (sSEC) to reversed-phase chromatography (RPC) expanded coverage of

67 tides increased retention of peptides during reversed-phase chromatography (RPC), particularly in the

68 lycosylated by PNGase F, and fractionated by reversed-phase chromatography (RPC).

69 rs to develop a highly selective ion-pairing reversed-phase chromatography separation for sgRNAs.

70 techniques and peptide retention modeling in reversed-phase chromatography to generate a data set suf

71 rst dimension are automatically subjected to reversed-phase chromatography to separate similarly size

72 NA derivatized amino acids was lengthened in reversed-phase chromatography to the extent that polar a

73 d through a combination of methods including reversed-phase chromatography, treatment with phosphatid

74 luorescent assay components are separated by reversed-phase chromatography under isocratic conditions

75 extracts of apple peels were fractionated by reversed phase chromatography using gradient elution of

76 ethanesulfonate, (3) sequential ion-exchange/reversed-phase chromatography using a single non-end-cap

77 14 to 36 carbon atoms are separated by C(8) reversed-phase chromatography using a water-methanol gra

78 (microcon filtration, molecular sieving, and reversed-phase chromatography), we unambiguously identif

79 etylation resulted in increased retention in reversed-phase chromatography, whereas methylation, incl

80 hylls and bacteriochlorophylls) was based on reversed-phase chromatography with a methanol-acetone gr

81 profiled by untargeted metabolomics, namely, reversed-phase chromatography with negative electrospray