G-Sep™ is a gel filtration resin comprised of ultrapure cross-linked dextran for desalting and buffer exchange in industrial applications. It exhibits high selectivity, superb resolution, low non-specific adsorption and robust chemical stability.
- Quickly desalts, removes contaminants and transfers to a new buffer in a single step.
- Excellent recovery and minimum sample dilution
- Available in prepacked SpinOUT™ Desalting columns for fast and convenient desalting
Molecules purified with G-Sep™ are separated according to size. Smaller molecules pass significantly slower through the column than larger molecules.
Two different G-Sep™ resins are available, G-Sep™ 25 and G-Sep™ 50. They differ in their degree of cross-linking and hence in their degree of swelling and their molecular fractionation range. G-Sep™ 25 is better suited for smaller molecules and G-Sep™ 50 is better suited for larger molecules. G-Sep™ 25 and G-Sep™ 50 are both available in 3 different particle sizes (Superfine, Fine, and Medium).
The molecular weight cut-off (MWCO) for G-Sep™ 25 is 5 kD for proteins and 10 bases for nucleic acids. The molecular weight cut-off (MWCO) for G-Sep™ 50 is 25 kD for proteins and 20 bases for nucleic acids.
Buffer and pH effects on resolution are minimal and purified biomolecules are not significantly diluted (1.5-fold) when processed using G-Sep™.
G-Sep™ is autoclavable at 121°C, pH 7 for 30 minutes and is stable in all commonly used buffers, including: 0.2M NaOH; 0.2M HCl; 1M acetic acid; 8M urea; 6M guanidine HCI; 1% SOS, 24% Ethanol; 30% Propanol; and 30% Acetonitrile.
Features| G-Sep™ 50 | Superfine | Fine | Medium |
| BioProcess resin | Yes | Yes | Yes |
| Matrix | Cross-linked dextran | Cross-linked dextran | Cross-linked dextran |
| Wet bead size | 40–100 µm | 40-160 µm | 100-300 µm |
| Dry bead size | 20–50 µm | 20–80 µm | 50-150 µm |
| Water regain | 4.80-5.20 mL/g | 4.80-5.20 mL/g | 4.80-5.20 mL/g |
| Swelling | 9-11 mL/g | 9-11 mL/g | 9-11 mL/g |
| MWCO (size exclusion) | below 25,000 Da | below 25,000 Da | below 25,000 Da |
| Fractionation range Mr Globular proteins | 1,000-30,000 Da | 1,000-30,000 Da | 1,000-30,000 Da |
| Fractionantion Mp Dextrans | 500-10,000 Da | 500-10,000 Da | 500-10,000 Da |
| pH Stability | 2.0-13.0 | 2.0-13.0 | 2.0-13.0 |
| Pressure Flow Specification | min 60 cm/h, pressure drop cm H2O/bed height=15, bed height 10 cm, column 5 cm i.d. | min 150 cm/h, bed height 10 cm, column 5 cm i.d. | min 150 cm/h, bed height 10 cm, column 5 cm i.d. |
- 4 to 30°C, dry resins. Used resins 4 to 8 °C in 20% Ethanol or 0.1 M NaOH
- Commonly used buffers, 0.2 M NaOH, 0.2 M HCl, 1 M acetic acid, 8 M urea, 6 M guanidine HCl, 1 % SDS, 24 % ethanol, 30 % porpanol, 30 % acetonitrile
Applications- Protein purification and contamination removal from samples
- For the desalting and buffer exchange of protein and nucleic acid solutions
- Separate proteins from peptides
- Desalt peptides