Application Notes:

• Comparison of STYROS™ 1R and 2R with a Silica C4 Stationary Phase.
   

• Fast Protein Separation on STYROS™ 1R and 2R.
   

• Comparison of STYROS™ 1R/XP and 1R/XH.
   

• Separation of Angiotensin Variants at Basic pH.
   

• High Performance Separation of Proteins on STYROS™ 1R/NB.
   

• Ultra Fast Separation of Proteins on Narrow Bore Columns.
   

• Quality Control of Proteins of Different Lots from the Same Supplier.
   

• Assessing Proteins Across Grades and Suppliers.
   

• Polymeric Hard Gel Media-HPLC vs. Soft Gel-FPLC in the Separation of Biomolecules.
   

• Fast Separation of Protein Isoforms with Fully Porous Hard Gel Media: Hemoglobins.
   

• Polymeric Gigaporous Strong Anion Exchangers: Bead Size Distribution versus Pore Size Distribution.
   

• Polymeric Gigaporous Strong Cation Exchangers: Bead Size Distribution versus Pore Size Distribution.
   

• High Speed Resolution: Efficient Use of Long, Narrow-bore Columns.
   

• Polymeric Gigaporous Strong Cation Exchangers: Effect of Capacity on Protein Resolution.
   

• Separation of IgG from Albumins in Commercial Production.
   

• Polymeric Gigaporous Anion Exchanger: Throughpores versus Superficial Pores.
   

• Polymeric Gigaporous Anion Exchanger : Performance at Low Flow Rates.
   

• Separation of Small Molecules on STYROS™ Q/XH.
   

• Resolving Efficiency of Longer Columns: case application with medium capacity cation exchanger.
   

• Metal Chelate Liquid Chromatography on Hard Gel Gigaporous Polymeric Media: Comparison with Soft Gel.
   

• Metal Chelate Liquid Chromatography on Hard Gel Gigaporous Polymeric Media: Tri-dentate IDA versus Five-dentate TED:
   

• Separation of Cytochrome c Isoform on STYROS™ SE: Strong cation exchanger.
   

• Fast Separation of IgG on STYROS™ HQ: High Capacity Polymeric Gigaporous Strong Anion Exchanger.
   

• Fast Separation of IgG, IgA and IgM on STYROS™ DEAE/NB: Narrow Bore Weak Anion Exchanger.
   

• Fast Detection of XELODA (Capecitabine) in Urine Sample with STYROS™ 2R/XH.
   

• StyrosZyme™ TPCK-Trypsin, Immobilized Enzyme on Polymeric Hard Gel Stationary Phase: Online Digestion of Lysozyme in 5 minutes.
   

• StyrosZyme™ TPCK-Trypsin, Immobilized Enzyme on Polymeric Hard Gel Stationary Phase: Online Digestion of Insulin Oxidized B-chain in 16 minutes.
   

• StyrosZyme™ Pepsin, Immobilized Enzyme on Polymeric Hard Gel Stationary Phase: On line digestion of Cytochrome c From Horse Heart and Bovine Heart.
   

• SIMULATED MONOLITH™: Fast Separations with HIC (Hydrophobic Interaction Chromatography)
   

• SIMULATED MONOLITH™: Comparison With Non Covalently Coated Polymeric Hard Gel.
   

• StyrosZyme™ Papain, Immobilized Enzyme on Simulated Monolith Polymeric Stationary Phase: Effect of Temperature and Linear Velocity on Online Digestion.
   

• Rapid isolation of IgG From Human Serum on STYROS™ rA (Immobilized Recombinant Protein A on Simulated Monolith Polymeric Stationary Phase).
   

• ADRIAMYCIN: Detection in Urine Sample with STYROS™ 2R/XH.
   

• Immobilized Protein rA on Polymeric Porous Hard Gel (STYROS™ rA): Comparison with Sepharose rA.
   

• NAVELBINE: Fast Detection in Urine Sample with STYROS™ 2R/XH.
   

• On Line Affinity capture of APROTININ on StyrosZyme™ TPCK-Trypsin, Immobilized Enzyme on Polymeric Hard Gel Stationary Phase.
   

• Separation of APROTININ from apo-Transferrin and Hexokinase on Polymeric Hard Gel Anion-Exchange Columns.
   

• APROTININ Purity Test on STYROS™ Anion and Cation Exchanger. Polymeric Hard Gel Stationary Phase.
   

• StyrosZyme™ Pepsin. Immobilized Enzyme on Polymeric Hard Gel Stationary Phase: On line digestion at 0º C and pH 2.5.
   
• Hydrophobic Interaction Chromatography compared with Polymeric Reversed Phase: STYROS™ HIC-Butyl versus STYROS™ 2R.
   
• Hydrophobic Interaction Chromatography : Comparison of STYROS™ HIC-Phenyl with Shodex HIC PH-818.
   
• Reversed Phase Polymeric: Comparison of STYROS™  2R with Commercial Non Porous Polymeric.
   

• Hydrophobic Interaction Chromatography: Comparison of STYROS™ HIC-Phenyl with TSKgel Phenyl-5PW from TOSOH.
   

• Hydrophobic Interaction Chromatography: Comparison of STYROS™ HIC-Butyl with TSKgel Butyl-NPR from TOSOH.
   

• Hydrophobic Interaction Chromatography: Comparison of STYROS™ HIC-Ether with TSKgel Ether-5PW from TOSOH.
   

• Separation of Hen Egg White Proteins: STYROS™ HQ Compared with Mono Q
   

• Low Salt Separations on Shielded Weak Anion Exchanger: STYROS™ SWAX
   
• STYROS™ 3R Simulated Monolith Polymeric Reversed Phase.
   
• STYROS™ 3R Simulated Monolith Polymeric Reversed Phase: Standard Separation of 6 Small Molecules
   
• STYROS™ Amino HILIC Simulated Monolith Polymeric Normal Phase: Standard Separations.
   
• STYROS™ Amino HILIC Simulated Monolith™  Polymeric: Separation of Benzoic Acid and Derivatives
   
• STYROS™ Amino HILIC Simulated Monolith™  Polymeric: Effect of Ionic Strength and Temperature on the Separation of Aromatic Acids
   

• STYROS™ Amino HILIC Simulated Monolith Polymeric: Separation of Angiotensins I, II and III

FYI Notes:

• Reversed Phase and Ion Exchange Chromatography of Two Proteins on STYROS™Columns.
   
• Effect of Long Residency Time and Heat During Reversed Phase Chromatography of Some Proteins.
   
• A Simple Alternative to Reduce Sample Consumption and Waste Generation by Over 40 %.
   
• Resolving Capabilities of a 25 cm Column Without the Flow and pH Restriction of Silica.
   
• STYROS™ Polymeric Stationary Phases as Compared with Silica.
   

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