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凝胶过滤预装柱Superdex 30 Increase
Superdex 30 Increase SEC columns are for high resolution, small-scale purification and analysis of small biomolecules with Mr ~ 100 to ~ 7000, such as peptides
Superdex Peptide 10/300 GL will be discontinued end of 2017 and replaced by Superdex 30 Increase 10/300 GL during 2017. Superdex Peptide 10/300 GL is a prepacked column for high-resolution size exclusion chromatography for small-scale preparative purification and analysis of peptides and other small biomolecules with molecular weights between 100 and 7000.
Superdex 30 Increase SEC columns are for high resolution, small-scale purification and analysis of small biomolecules with Mr ~ 100 to ~ 7000, such as peptides
Superdex 30 Increase is part of Cytiva's new generation of agarose-based SEC columns called “Increase”, which offer higher resolution purification in shorter runtimes compared with their predecessors.
Superdex 30 Increase is suitable for both preparative and analytical purposes.
The fractionation range allows preparative separation of peptides, oligosaccharides and other small biomolecules (Mr ~ 100 to ~ 7000) with sample volumes up to 500 µL.
These columns also enable protein characterization, including aggregate analysis, size homogeneity analysis, and interaction studies, where high-quality data can be achieved
This agarose-based resin is alkali resistant and supports cleaning-in-place (CIP) procedures. This capability allows the same column to be used for different biomolecules, with minimal risk of carry-over between samples.
Regular cleaning can also increase column lifetime.
Two size exclusion chromatography (SEC) column sizes are designed to serve different purposes:
Parameter
Superdex 30 Increase 10/300 GL
Bed dimensions 10 × 300 mm
Bed height 300 to 310 mm
Bed support Filter
Bed volume ~ 24 mL
Chemical stability Conditions where the resin may be operated without significant change in function:
• Trifluoroacetic acid, up to 0.2%
• Isopropanol, up to 5%
• Dithiothreitol (DTT), up to 5 mM
• Acetonitrile, up to 70%
• Formic acid, up to 1%
• All commonly used aqueous buffers, pH 3 to 12
• Urea, up to 8 M
• Guanidine hydrochloride, up to 6 M
• Ionic and nonionic detergents, e.g., 1% SDS
• Methanol, up to 70%
Conditions where the resin can be subjected to cleaning- or sanitization-in-place without significant change in function:
• Sodium hydroxide, up to 1 M
• Ethanol, up to 70%
• Isopropanol, up to 30%
• Hydrochloric acid, up to 0.1 M
• Trifluoroacetic acid, up to 1%
• Dimethyl sulfoxide (DMSO), up to 10%
Avoid:
• Oxidizing agents
• Unfiltered samples and eluents
Chemical stability (column hardware) Resistant to most solutions used in liquid chromatography except hydrocarbons, aromatic solvents and chlorinated hydrocarbons.
Column i.d. 10 mm
Fractionation range (Mr) (globular proteins) 100 to 7000
Material (column hardware) Borosilicate glass, polyetheretherketone (PEEK), polypropylene (PP), ethylene propylene diene monomer (EPDM), and perfluoro-rubber (PFR)
Material (bed support) Polyethylene (PE) filter
Material (column tube) Borosilicate glass
Matrix Composite of cross-linked agarose and dextran
Operating flow rate, max. 1.2 mL/min, water at room temperature;
0.60 mL/min, 20% ethanol or 10% glycerol at room temperature;
0.60 mL/min water at low temperature;
0.30 mL/min 20% ethanol or 10% glycerol at low temperature
Operating flow rate, recommended1 0.80 mL/min
Particle size, d50V2 ~ 9 µm
Sample volume 25 to 500 µL
Storage conditions 4˚C to 30˚C, 20% ethanol
Theoretical plates > 43 000 m-1
Typical pressure drop over the packed bed3 ~ 3 MPa
pH stability, cleaning-in-place (CIP) 1 to 14
pH stability, operational 3 to 12
1、Water at 20˚C to 25˚C.
2、Median particle size of the cumulative volume distribution.
3、At 25˚C in water. Determine the individual column limit according to product instructions for use.

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