𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Selectivity optimization of reversed-phase high-performance liquid chromatographic peptide and protein separations by varying bonded-phase functionality

✍ Scribed by Barry E. Boyes; Douglas G. Walker

Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
942 KB
Volume
691
Category
Article
ISSN
1873-3778

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Separation of peptides by reverse-phase
Separation of peptides by reverse-phase high-performance liquid chromatography using propyl- and cyanopropylsilyl supports
✍ Paul Tempst; Michael W. Hunkapiller; Leroy E. Hood πŸ“‚ Article πŸ“… 1984 πŸ› Elsevier Science 🌐 English βš– 639 KB

The separation of peptides and proteins by reverse-phase high-performance liquid chromatography with cyanopropylsilyl and large-pore propylsilyl supports, together with aqueous trifluoroacetic acid/acetonitrile gradients, was studied. Operating parameters (trifluoroacetic acid concentration, flow ra

Rapid separation of proteins and peptide
Rapid separation of proteins and peptides by reversed-phase microcolumn liquid chromatography
✍ Norikazu Nagae; Hiroko Itoh; Noriyuki Nimura; Toshio Kinoshita; Toyohide Takeuch πŸ“‚ Article πŸ“… 1991 πŸ› John Wiley and Sons 🌐 English βš– 357 KB πŸ‘ 1 views

Proteins and peptides were separated in the reversed-phase mode on microcolumns packed with nonporous octadecyl-group bonded silica gel with an average particle diameter of 4.5 or 20 pm. Separation columns were prepared from glass-lined stainless steel tubing of 39 or 56-mm x 0.5-mm i.d. An artifici

Use of binary and ternary mobile phases
Use of binary and ternary mobile phases in reversed-phase high performance liquid chromatographic separation of chiral compounds
✍ WΕ‚adysΕ‚aw GoΕ‚kiewicz; Anna BΕ‚aΕΌewicz; Dariusz Matosiuk πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 465 KB

## Abstract The influence of the nature of typical organic modifiers, used in reversed‐phase systems diluted with water, on retention and selectivity of chiral acetylated diamines and acetonitriles possessing pharmacological activity was investigated. Linear, semilogarithmic relationships between t