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

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

2 urified by size exclusion chromatography and reversed phase chromatography.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

34 Reversed phase chromatography, electrospray ionization-M

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

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

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

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

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

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

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

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

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

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

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

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

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

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

49 Reversed-phase chromatography revealed that most SAR11 b

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

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

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

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

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

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

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

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

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

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

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

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

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

63 14 to 36 carbon atoms are separated by C(8) reversed-phase chromatography using a water-methanol gra

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

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