Cation exchange columns
strong and weak cation exchange
Suitable for biomolecules like proteins, peptides, DNA, RNA
Product information
Ion exchange chromatography is an analytical method relying on the interaction of ion-charges between the surface of proteins and the surface of the packing material. Packing materials with a positive surface charge are called “anion exchangers” and those with a negative surface charge are called “cation exchangers”.
A strong cation exchange resin with a sulfopropyl functional group is packed into the IEC SP-825 and IEC SP-FT 4A column. This columns can be used at a wider pH range because the pKa of the ion exchange base is 2.3.
IEC SP-825
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Suitable for analyzing relatively high molecular weight compounds: proteins, peptides, DNA, and RNA
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Usable in a wide pH range from pH 2 to 12
IEC SP-FT 4A
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Non-porous base material
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Provides ultra-rapid analysis using conventional devices
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PEEK housing
IEC CM-825 and Asahipak ES-502C are packed with a weak cation exchange resin with Carboxymethyl as the functional group. These
columns are suitable for the separation of basic proteins because the pKa of the ion exchange base is 5.7.
IEC CM-825
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Suitable for analyzing relatively high molecular weight compounds: proteins, peptides, DNA, and RNA
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Usable in a wide pH range from pH 2 to 12
Asahipak ES-502C 7C
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Compared to IEC series columns, polyvinyl alcohol is used as base material offering different separation pattern
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Low hydrophobic interaction with proteins allows analysis under mild conditions
CXpak P-421 is a strong cation exchange column filled with spherical porous particles of styrene divinylbenzene copolymer. It is an ideal column for analyzing various amino acids. CXpak P-421 is used with an amino acid analyzer with post-column derivatization method.
CXpak P-421S
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Column for amino acids analysis by cation exchange mode
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Provides simultaneous analysis of different amino acids
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Fulfills USP L22 and L58 requirements
Obtaining some information about the isoelectric point (pI) of proteins is useful for selecting suitable analytical conditions. Proteins consist of amino acids, and are amphoteric compounds, so there is pH at which the total sum of electrical charges becomes zero in the solution. That pH is called isoelectric point (pI). Around the pI, the electrical charge on the surface of proteins is neutralized and such proteins cannot easily adsorb on the surface of the packing material. In some cases, proteins precipitate around the pI, a phenomenon known as “isoelectric precipitation”. In order to adsorb the target protein, the pH of the eluent must be adjusted at more than 1.0 pH unit from pI. When the pH is more acidic than the pI, a cation exchanger should be used, and when the pH is more alkaline than the pI, an anion exchanger should be selected.
Product overview
Product code | Product name | Separation | Functional group | Gel material | Plates per column | Particle size | Pore size | Size (ID x length) | Housing material |
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F6118250 | IEC SP-825 | Ion Exchange | Sulfopropyl | Polyhydroxy-methacrylate | ≥ 2,000 | 8 µm | 5,000 Å | 8.0 x 75 mm | steel |
F6113100 | IEC SP-FT 4A | Ion Exchange | Sulfopropyl | Polyhydroxy-methacrylate | ≥ 20,000 | 2.7 µm | - | 4.6 x 10 mm | PEEK |
F6110002 | IEC CM-825 | Ion Exchange | Carboxymethyl | Polyhydroxy-methacrylate | ≥ 2,000 | 8 µm | 5,000 Å | 8.0 x 75 mm | steel |
F7640001 | Asahipak ES-502C 7C | Ion Exchange | Carboxymethyl | Polyvinyl alcohol | ≥ 3,300 | 9 µm | 2,000 Å | 7.5 x 100 mm | steel |
F6354211 | CXpak P-421S | Ion Exchange | Sulfo (Na+) | Styrene divinylbenzene copolymer | ≥ 3,500 | 6 µm | - | 4.6 x 150 mm | steel |
F6700210 | CXpak P-G | Ion Exchange | Sulfo (Na+) | Styrene divinylbenzene copolymer | (guard) | 6 µm | - | 4.6 x 10 mm | steel |
Product details
Product name | Maximum pressure | Usual flow rate | Maximum flow rate | Temperature range | pH range | Salt concentration | Shipping solvent | USP | Info |
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IEC SP-825 | 2 MPa (20 bar) | 1.0 mL/min | 1.5 mL/min | 10 to 50°C | 2 to 12 | 20 mM to 1.0 M | 50 mM Na2SO4 aq. | - | 0.4 meq/g Ion-exchange capacity |
IEC SP-FT 4A | 20 MPa (200 bar) | 1.0 mL/min | 3.0 mL/min | 5 to 45°C | 2 to 12 | ≤ 1.5 M | 20 mM 2-(N-Morpholino)ethanesulfonic acid buffer (pH 5.6) | - | 0.2 meq/g Ion-exchange capacity |
IEC CM-825 | 2 MPa (20 bar) | 1.0 mL/min | 1.5 mL/min | 10 to 50°C | 2 to 12 | 20 mM to 1.0 M | 50 mM Na2SO4 aq. | - | 0.4 meq/g Ion-exchange capacity |
Asahipak ES-502C 7C | 1.2 MPa (20 bar) | 1.0 mL/min | 1.5 mL/min | 10 to 50°C | 2 to 12 | 20 mM to 0.6 M | 0.1 M Sodium phosphate buffer (pH 4.4) | - | 0.55 meq/g Ion-exchange capacity |
CXpak P-421S | 5 MPa (50 bar) | 0.5 mL/min | 0.7 mL/min | 15 to 63°C | ≥ 3 | - | H2O | L22, L58 | - |
CXpak P-G | - | - | - | 15 to 63°C | ≥ 3 | - | H2O | L22, L58 | - |
Applications
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IEC SP-825
Analysis of Thaumatin (SP-825)
Effects of pH on Elution Pattern (SP-825)
Effects of Sample Load on Peak Width (SP-825)
Recovery of Proteins and Enzyme Activity (SP-825)
Standard Proteins (7) (CM-825, SP-825)
IEC SP-FT 4A
Charge Variant Analysis of Cetuximab (SP-FT 4A)
Charge Variant Analysis of Cetuximab (2) (SP-FT 4A)
Charge Variant Analysis of Trastuzumab (SP-FT 4A)
Effects of Flow Rate for Protein Analysis (SP-FT 4A)
Ultra-rapid Analysis of Hemoglobin A, F, S and C (SP-FT 4A)
Ultra-rapid Analysis of Standard Proteins (SP-FT 4A)
IEC CM-825
Effects of Sample Load on Resolution (CM-825)
Recovery of Proteins and Enzyme Activity (CM-825)
Ribonuclease A from Equine Pancreas (CM-825)
Standard Proteins (7) (CM-825, SP-825)
Asahipak ES-502C 7C
Analysis of Pochonicine and Its Analogues in Filamentous Fungi Culture Extract
Analysis of Uric Acid and Creatinine using Column Switching Method
Carcinogenic Tryptophan Pyrolysis Products
Catecholamines (3) (ES-502C 7C)
Catecholamines in Urine (ES-502C 7C)
Cytochrome P450 in Rat Liver Microsome
Mild Hydrolysates of Allosamidin
Paraquat and Diquat (ES-502C 7C)
Standard Proteins (8) (ES-502C 7C)
CXpak P-421S