Q Cross-linked Agarose High Performance
Q Cross-linked Agarose High Performance has well-deserved reputations as highly successful anion and cation ion exchange media for purifying a wide range of biomolecules.
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Description:
Glutathione S-transferase (GST) gene fusion systems have been widely used for obtaining large amounts of desirable protein in Escherichia coli. The fusion protein, which contains a GST tail can then be purified through affinity chromatography. MCLAB’s glutathione agarose is designed for the specific purification of GST recombinant proteins and other glutathione-binding proteins. Glutathione agarose is uniquely formulated for excellent binding capacity and purity of the protein of interest.
Specifications
|
Chromatography technique |
GST-tagged protein purification |
|
Matrix |
Highly cross-linked 6% beaded agarose |
|
Active group |
Glutathione |
|
Active group density |
>40 umol/ml drained medium |
|
Spacer |
1,4-bis(2,3-epoxypropoxy)butane (12 atom stable and uncharged ether hydrophilic linkage) |
|
Bead geometry & size |
Spherical 50 to 150 um |
|
Bead mean diameter d50v |
90 um |
|
Linear flow velocity |
<75 cm/h at 25 °C, HR 16/10 column, 5 cm bed height |
|
Recommended linear flow rate |
<30 cm/h |
|
Pressure/flow specification |
Base matrix 100-200 cm/h, pressure drop cm H2O/bed height = 15, bed height 10 cm, 5 cm i.d. |
|
1ml Cartridge bed dimensions |
7×25 mm |
|
1ml Cartridge bed height |
25 mm |
|
1ml Cartridge bed volume |
1 ml |
|
1ml Cartridge column I.D |
7 mm |
|
5ml Cartridge bed dimensions |
16×25 mm |
|
5ml Cartridge bed height |
25 mm |
|
5ml Cartridge bed volume |
5 ml |
|
5ml Cartridge column I.D |
16 mm |
|
Maximum cartridge flow rate |
5 ml/min (1 ml cartridge) or 20 ml/min (5ml cartridge) |
|
Recommended cartridge flow rate |
1 ml/min (1 ml cartridge) or 5 ml/min (5 ml cartridge) |
|
Maximum pressure during operation |
5 bar [0.5 MPa] (70 psi) |
|
pH Stability working range |
3 to 13 |
|
pH Stability cleaning in place (cip) |
2 to 14 |
|
Chemical stability |
Stable to commonly used aqueous solutions. Can be used with non-ionic detergents, denaturing solvents, e.g. 8 M urea and 6 M guanidine hydrochloride, Stable in organic solvents, e.g. 50% methylformamide and 50% dioxane. |
|
Storage |
2 to 8 °C |
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Q Cross-linked Agarose High Performance has well-deserved reputations as highly successful anion and cation ion exchange media for purifying a wide range of biomolecules.
Used in proteomics and protein chromatography, amino acid agarose is prepared by covalently coupling of amino acid through a 17 atom stable and uncharged ether hydrophilic linkage to highly cross-linked 6% agarose with bead mean diameter of 90 um.
Glutathione S-transferase (GST) gene fusion systems have been widely used for obtaining large amounts of desirable protein in Escherichia coli.
Epoxy-activated Agarose is a pre-activated affinity chromatography support for the immobilization of a variety of biomolecules that contain nucleophiles, such as hydroxyl, amino, or thiol groups. These groups couple to the epoxy groups on the support, which is then used for the purification of proteins, carbohydrates, or DNA.
Recombinant Protein A is an immunoglobulin-binding protein derived from the cell wall of the bacterium Staphylococcus aureus.
Ni2+, Co2+, Cu2+, or Zn2+ charged nitrilotriacetic acid (NTA) coupled to Agarose CL-6B via a stable and uncharged long ether hydrophilic spacer arm, and offers high binding capacity and minimal non-specific binding.
SP Cross-linked Agarose Big Beads are strong ion exchangers designed for industrial applications. The large particle sizes (100-300 µm) and excellent physical stability of the base matrix ensure maintained speed even with viscous samples.
Glutathione S-transferase (GST) gene fusion systems have been widely used for obtaining large amounts of desirable protein in Escherichia coli.
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