Size Exclusion Chromatography



Similar documents
Bio-Gel P Polyacrylamide Gel Instruction Manual

Guide to Reverse Phase SpinColumns Chromatography for Sample Prep

Data File. Sephadex G-25 media and pre-packed columns. Introduction. Sephadex G-25 Bead structure. Desalting/buffer exchange and gel filtration

AFFINITY CHROMATOGRAPHY

RESOURCE Q, 1 ml and 6 ml RESOURCE S, 1 ml and 6 ml

Gel Filtration Standard

Size Exclusion Chromatography

Blue Sepharose 6 Fast Flow

INSTRUCTIONS Edition AC

Corning Spin-X UF Concentrator Selection and Use Guide

Hydrophobic Interaction Chromatography

Method Development for Size-Exclusion Chromatography of Monoclonal Antibodies and Higher Order Aggregates

TECHNICAL BULLETIN. HIS-Select Nickel Affinity Gel. Catalog Number P6611 Storage Temperature 2 8 C

Solid Phase Extraction Products PAGE: 1. Introduction of Solid Phase Extraction (SPE) Why Choose Nano-Micro Tech SPE

Aspects of industrial purification of peptides using large-scale chromatography. Lars Andersson and Jonas Persson

HiTrap Heparin HP, 1 ml and 5 ml

Affi-Prep Protein A Matrix Instruction Manual

Protein purification methods, a practical approach

Reading instructions to partitioning in aqueous two-phase systems

PRODUCT INFORMATION Chromalite resins for reverse-phase chromatography, adsorption and SPE

Marmara Üniversitesi Fen-Edebiyat Fakültesi Kimya Bölümü / Biyokimya Anabilim Dalı PURIFICATION AND CHARACTERIZATION OF PROTEINS

Chemical Structure of the polymer showing end groups: CH 3 CH 2 CH H

POROS CaptureSelect affinity columns for highspeed quantification of IgG Fc fusion proteins

ENrich SEC 70 ENrich SEC 650 High-Resolution Size Exclusion Columns Instruction Manual

LUMEFANTRINE Draft proposal for The International Pharmacopoeia (October 2006)

6 Characterization of Casein and Bovine Serum Albumin

SPE and HPLC. Dr Iva Chianella Lecturer in Analytical Chemistry Cranfield Health +44 (0)

Reversed Phase Chromatography

Diffusion and Fluid Flow


GE Healthcare. Hydrophobic Interaction and Reversed Phase Chromatography. Principles and Methods

The Theory of HPLC. Gradient HPLC

Purification of reaction mixtures using flash chromatography.

Applications of Organic Solvent Nanofiltration in the Process Development of Active Pharmaceutical Ingredients. Dominic Ormerod

An Advanced Base Deactivated Capillary Column for analysis of Volatile amines Ammonia and Alcohols.

HiTrap Chelating HP, 1 ml and 5 ml

This handbook presents the basic principles of reversed-phase HPLC for the

The Essential CHROMacademy Guide. Mobile Phase Optimization Strategies for Reversed Phase HPLC

Pipette Tips PACKARD BIOSCIENCE MultiPROBE II COMPATIBLE

About the Kits...2 Description 2 Components 2. Factor Xa Cleavage...3 Small scale optimization 3 Scale-up 3 Monitoring cleavage 4

(c) How would your answers to problem (a) change if the molecular weight of the protein was 100,000 Dalton?

POROS CaptureSelect affinity columns for rapid, small-scale purification and sample preparation of recombinant proteins

A Guide to the Analysis and Purification of Proteins and Peptides by Reversed-Phase HPLC

Aurum Ion Exchange Mini Kits and Columns. Instruction Manual

Application Note. Determination of Nitrite and Nitrate in Fruit Juices by UV Detection. Summary. Introduction. Experimental Sample Preparation

PrepTip. Reverse Phase PrepTip User Guide

IAM Chromatography. HPLC Separation Tools for Membrane Protein Purification and Drug Membrane Permeability Prediction

Separation of Amino Acids by Paper Chromatography

ERDOSTEINE - MONOGRAPH.

Tamsulosin Hydrochloride Capsules

Experiment #10: Liquids, Liquid Mixtures and Solutions

Selectivity and Detectability Optimizations in HPLC

MabSelect SuRe. GE Healthcare Life Sciences

Application Note. Determination of Amino acids by UHPLC with automated OPA- Derivatization by the Autosampler. Summary. Fig. 1.

Expression and Purification of Recombinant Protein in bacteria and Yeast. Presented By: Puspa pandey, Mohit sachdeva & Ming yu

Process-scale purification of monoclonal antibodies polishing using Capto Q

High-Throughput 3-D Chromatography Through Ion Exchange SPE

Application Note. Separation of three monoclonal antibody variants using MCSGP. Summary

Recombinant Enterokinase Kits

PROTEIN SEQUENCING. First Sequence

Affinity Chromatography

Troubleshooting Guide for DNA Electrophoresis

AG 501-X8 and Bio-Rex MSZ 501(D) Mixed Bed Resin Instruction Manual. Bio-Rad Laboratories, 2000 Alfred Nobel Dr., Hercules CA LIT205 Rev B

Thermo Scientific Syncronis HPLC Columns. Technical Manual

TANNIC ACID. SYNONYMS Tannins (food grade), gallotannic acid, INS No. 181 DEFINITION DESCRIPTION

Continuous Chromatography for Monoclonal Antibody Purification from Cell Culture Supernatant

Structures of Proteins. Primary structure - amino acid sequence

--not necessarily a protein! (all proteins are polypeptides, but the converse is not true)

Monoclonal Antibody Fragment Separation and Characterization Using Size Exclusion Chromatography Coupled with Mass Spectrometry

Carbohydrates, proteins and lipids

DOWEX Resins as Organic Solvent Desiccants

An In-Gel Digestion Protocol

Protein Separation Technology

Extraction and Properties of the Polyphenol, Catechin, as an Antioxidant

Bulk Materials for Preparative and Process Chromatography

α-cyclodextrin SYNONYMS α-schardinger dextrin, α-dextrin, cyclohexaamylose, cyclomaltohexaose, α- cycloamylase

Size Exclusion Chromatography

The Organic Chemistry of Amino Acids, Peptides, and Proteins

1.1 This test method covers the qualitative and quantitative determination of the content of benzene and toluene in hydrocarbon wax.

for SolEx TM HRP Cartridges SolEx TM HRP RSLC Columns

[ Care and Use Manual ] styragel column. Contents. I. Introduction. II. Installing the Column Bank. III. Preparing Solvent and Samples

SUCRALOSE. White to off-white, practically odourless crystalline powder

serum protein and A/ G ratio

CHEMISTRY STANDARDS BASED RUBRIC ATOMIC STRUCTURE AND BONDING

Analyzing Small Molecules by EI and GC-MS. July 2014

HiPer Ion Exchange Chromatography Teaching Kit

Absorption of Drugs. Transport of a drug from the GI tract

Name Lab #3: Solubility of Organic Compounds Objectives: Introduction: soluble insoluble partially soluble miscible immiscible

A. A peptide with 12 amino acids has the following amino acid composition: 2 Met, 1 Tyr, 1 Trp, 2 Glu, 1 Lys, 1 Arg, 1 Thr, 1 Asn, 1 Ile, 1 Cys

Research for leachables of nuclear grade cation exchange resin

Electrospray Ion Trap Mass Spectrometry. Introduction

Protein Purification Handbook

Ch18_PT MULTIPLE CHOICE. Choose the one alternative that best completes the statement or answers the question.

Effect of temperature and ph on the enzymatic activity of salivary amylase

Gas Chromatography. Let s begin with an example problem: SPME head space analysis of pesticides in tea and follow-up analysis by high speed GC.

Materials for Pharmaceutical Manufacturing

HisTrap HP, 1 ml and 5 ml

Disaccharides consist of two monosaccharide monomers covalently linked by a glycosidic bond. They function in sugar transport.

POLYVINYL ALCOHOL. SYNONYMS Vinyl alcohol polymer, PVOH, INS No DEFINITION DESCRIPTION FUNCTIONAL USES CHARACTERISTICS

Transcription:

Size Exclusion Chromatography TOYOPEARL Resins for SEC TOYOPEARL TOYOPEARL TOYOPEARL HW-55 TOYOPEARL HW-65 TOYOPEARL TOSOH BIOSCIENCE TOSOH BIOSCIENCE LLC 56 Keystone Drive Montgomeryville, PA 896-967 Orders & Service: (800)66-875 Fax: (5)8-505 www.tosohbioscience.com Email: TOSOH info.sep.am@tosohbioscience.com BIOSCIENCE

Size Exclusion Chromatography TOYOPEARL Size Exclusion Chromatography Size exclusion chromatography, also known as gel filtration, separates molecules in aqueous solution according to their size as they pass through a porous structure. Molecules with a diameter greater than the largest pores within the resin material are unable to enter the particle. Because they pass through the smallest accessible volume, they travel through the column and elute Features small particles available first. Smaller molecules, which are able to access pores within the resin particles, pass through a larger accessible volume within the column depending on their apparent size and are eluted later, in order of decreasing molecular weight. SEC is a mild, non-adsorption technique and is a non-destructive method for determining molecular weights. It is also used for Benefits high resolution hydrophilic porous polymer structure minimal non-specific adsorption effects narrow particle size distribution good mechanical stability chemically stable (ph - ) identical resin chemistry to TSK-GEL PW HPLC resins high performance SEC excellent flow characteristics in large industrial size columns (up to bar) constant packing volume over a wide range of salt concentrations compatible with organic solvents, can be cleaned in place with acid or base temperature stable polymer may be run at elevated temperature ( - 60 C), autoclavable at C direct scale-up from TSK-GEL PW HPLC columns Table I Properties and molecular weight separation ranges for TOYOPEARL HW resins (HW = Hydrophilic, Water-compatible polymeric base resins) Molecular weight of sample (Da) TOYOPEARL Particle Pore Polyethylene Dextrans Globular resin size (µm) size (Å) glycols and oxides proteins S 0-0 50 00 -,000 00-7,000 00 0,000 F 0-60 C 50-00 S 0-0 5 00-8,000 500-0,000 500-80,000 F 0-60 HW-55S 0-0 500 00-50,000,000-00,000,000-700,000 HW-55F 0-60 HW-65S 0-0 000 500 -,000,000 0,000 -,000,000 0,000-5,000,000 HW-65F 0-60 F 0-60 > 000,000-5,000,000 00,000-0,000,000 500,000-50,000,000 0 TOSOH BIOSCIENCE -800-66-875

Pore Size process scale purification, often as a final stage polishing step to separate multimers, or molecular fractions or as a means of buffer exchange or desalting. Because it does not rely upon adsorption of the molecule to the resin, SEC is characterized by dilution of the loaded product. Resins suited to SEC feature a predefined exclusion limit together with a fractionation range, governed respectively by the maximum pore size and pore size distribution. These important variables are controlled during manufacture. Pore Size The TOYOPEARL range includes 5 pore sizes covering 5 different fractionation ranges. The choice of resin depends on the molecular weight of the sample components; this information is shown for proteins, dextrans and PEG polymers in Table I and II. The TOYOPEARL HW resin range spans peptide and protein molecular weights between 00-50,000,000 Daltons. Each TOYOPEARL HW resin displays a typical calibration curve and exclusion limit for globular proteins (Figure ). Table II Figure Log MW (Da) Calibration curves for globular proteins on TOYOPEARL resins 7 6 5 HW-55 HW-65 0.0 0.0 0.50 0.60 0.70 0.80 Ve / Vc Column: mm I.D. x 0 cm L Sample: protein standards Elution: 0.06 M phosphate buffer (ph 7.0) in 0.06 M KCl Legend: Ve = elution volume, Vc = column volume 0 0 0 0 5 0 6 0 7 Leucine Vitamin B HW-55 * ACTH Insulin Cytochrome C α Human γ HW-65 ** Aldolase Catalase Urease Thyroglobulin Blue Dextra n Hemocyanin Poliovirus RNA a) Globular proteins * and ** Base materials for IEC supports ** Base material for HIC and AFC supports Calibration molecules HW-55 HW-65 b) Dextrans HW-55 c) Polyethylene glycols HW-65 TOSOH BIOSCIENCE For ordering information, see page.

Size Exclusion Chromatography Particle Size Resolution is increased with decreasing particle size. Resin particle size is proportional to HETP and consequently inversely proportional to resolution of two peaks. TOYOPEARL HW resins are available in three particle size ranges: S-grade = 0-0 µm (superfine) F-grade = 0-60 µm (fine) C-grade = 50-00 µm (coarse) Figure Comparison of resolution on different particle sizes of TOYOPEARL HW-55 Mobile phase Mobile phase components, such as neutral salts, can affect SEC separations. The presence or absence of sodium chloride influences the elution volume of proteins. This can be seen in Figure, in which a mixture of various proteins was separated on a column of TOYOPEARL HW-55F. In most cases it is desirable to select a salt concentration which minimizes secondary interactions of the sample components with the resin. However, there are instances where secondary interactions, particularly hydrophobic interactions at higher salt concentrations, can be taken advantage of by increasing salt concentration in the mobile phase. Figure Comparison of the elution volumes of proteins in presence and absence of NaCI Urease (pl.8-5.) C-grade 5.5 Catalase (pl 5.5) F-grade 5.0 Log MW5.5.0 Porcine Pepsin (pl ~.0) Subtilisin BPN (pl 9.) Yeast ADH (pl 5.) Apo Transferrin (pl 5.5) Hemoglobin (pl 6.8-7.0) C A (pl 9.5) L Cytochrome C (pl 0.6) S-grade 60 80 00 0 0 60 80 Elution Volume (ml) Column: TOYOPEARL HW-55F, mm I.D. x 50cm Elution: 5 mm Tris-HCl with ( ) or without ( ) 0.5 M NaCl, (ph 7.5) Flow rate: 6 cm/h Temperature: 5-0 C Detection: UV @ 80 nm, 0 nm for heme proteins, 00 nm for non-aromatic amino acids.5.5 Elution Time (hr) Column: Eluent: Flow rate: Temperature: Detector: Sample: Inj. Volume: TOYOPEARL HW-55, 6 mmid x 70cm /0 M Phosphate buffer (ph 7.0), 0.M NaCI 06mL/h (0cm/h) 5 C UV@80 nm. Thyroglobulin (0.%). γ-globulin (0.%). γ-lactoglobulin (0.%). Cytochrome C (0.%) ml TOSOH BIOSCIENCE -800-66-875

Properties Properties in aqueous solvent high mechanical stability TOYOPEARL Resins have excellent mechanical properties, the gels can be operated at pressures up to bar without deformation. minimum change in gel bed volume Alterations of the bed volume when the eluent is changed, be it buffer with varous ph values and/or different salt concentrations, are negligible. This is a great advantage particularly in elution with salt gradients. TOYOPEARL does not shrink or swell even in high concentrations of strong denaturating agents such as urea or guanidine hydrochloride. chemical stability Conventional gels are usually sensitive to acid and alkaline hydrolysis. TOYOPEARL, however, is stable from ph -, and tolerant to ph 0- for short periods. Substances which are only soluble at extreme ph values can be readily separated. sharp chromatographic peaks Sample dilution after separation on TOYOPEARL is particulary small, due to the small uniform particle size and the narrow particle-size range (min. 90% within declared limits). This property is particularly important when isolating high-value substances and in large-scale industrial separations. temperature stability TOYOPEARL is thermally stable and does not degrade or denature even in boiling water. TOYOPEARL resins can be sterilized by autoclaving at C. microorganism resistance TOYOPEARL is an organosynthetic material, and is resistant to degradation by microorganisms. Growth of microbes is inhibited by storing the gels in 0% ethanol. suitability for affinity chromatography and enzyme immobilization TOYOPEARL resins contain numerous hydroxyl groups on the external and internal surfaces of the resin. These, in combination with the chemical stability of the polymer, render the gels particulary suited to covalently bonding enzymes or other ligands. When fast flow supports are required, TOYOPEARL HW- 65 is the base resin of choice. Properties in organic solvent partition and adsorption effects TOYOPEARL can be used in organic solvents or mixtures of organic solvents and water. Bed volumns swell or shrink relative to water depending on the solvent as show in Figure. As seen in Table III, TOYOPEARL also swells in polar organic solvents. In general, however, the bed volume decreases slightly with decreasing solvent polarity. DMSO can be used for SEC of oligosaccharides and polyethylene glycols. The compatibility of DMF with TOYOPEARL also permits SEC separation of hydrophobic substances such as polystyrenes. Figure Swelling properties of TOYOPEARL in various solvents Gel volume with various solvents/gel in water.5.0 0.5 H O MeOH DMSO DMF Acetone Ethyl acetate Benzene CHCI Toluene CHCI /MeOH (:) Table III Swelling properties in various solvents TOYOPEARL Water KCI aq 0. M MeOH EtOH DMF Acetone Toluene 00 00 00 00 0 80 65 00 00 00 00 0 80 70 HW-55 00 00 00 00 05 85 70 HW-65 00 00 00 00 05 90 75 00 00 05 0 0 0 90 TOSOH BIOSCIENCE For ordering information, see page.

Size Exclusion Chromatography Ordering Information TOYOPEARL LABPAK: Part # Product description Container Particle size (ml) size (µm) 98 SECPAK LMW (F, F, HW-55F) x 50 0-60 989 SECPAK HMW (HW-55F, HW-65F, F) x 50 0-60 980 SECPAK HP (S, S, HW-55S, HW-65S) x 50 0-0 TOYOPEARL SEC resins: Part # Product description Container Particle Exclusion size (ml) size (µm) limit (Da) 9809 S 50 0-0 x 0 075 50 077 500 68,000 07967 5,000 9808 F 50 0-60 x 0 078 500 68,000 07968 5,000 9807 C 50 50-00 x 0 079 500 68,000 07969 5,000 98 S 50 0-0.8 x 0 0755 50 075 500 68,000 08059 5,000 980 F 50 0-60.8 x 0 075 500 685,000 08060 5,000 98 HW-55S 50 0-0.5 x 0 5 0759 50 0756 500 686,000 0806 5,000 98 HW-55F 50 0-60.5 x 0 5 0757 500 687,000 0806 5,000 985 HW-65S 50 0-0 x 0 6 0767 50 076 500 688,000 08068 5,000 98 HW-65F 50 0-60 x 0 6 0765 500 689,000 08069 5,000 986 F 50 0-60 5 x 0 7 0769 500 69,000 0807 5,000 077 S 50 0-0 x 0 6 0768 500 0807 5,000 Conditions: Exclusion limits are +/- 0% and are determined using polyethylene glycol, polyethylene oxide, or dextran standards, as appropriate. TOSOH BIOSCIENCE -800-66-875