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Catalog No. CYT29091596
Part No. 29091596
Supplier Cytiva
Superose™ 6 Increase 10/300 GL
Net Price
3012
Availability

4 weeks

PROPERTIES
  • Bed volume
    ~ 24 mL
  • Bed height
    300 to 310 mm
  • Bed support
    Filter
  • Material (bed support)
    Polyethylene (PE) filter
  • Material (column tube)
    Borosilicate glass
  • Column i.d.
    10
  • Chemical stability
    Conditions where the resin may be operated without significant change in function:
    • All commonly used aqueous buffers, pH 3 to 12
    • Urea, up to 8 M
    • Ionic and nonionic detergents, e.g., 1% SDS
    • Guanidine hydrochloride, up to 6 M
    • Isopropanol, up to 5%
    • Methanol, up to 10%
    • Sodium hydroxide, up to 0.5 M
    • Dithiothreitol, up to 5 mM
    Conditions where the resin can be subjected to cleaning- or sanitization-in-place without significant change in function:
    • Acetonitrile, up to 30%
    • Sodium hydroxide, up to 1 M
    • Ethanol, up to 70%
    • Methanol, up to 100%
    • Acetic acid, up to 1 M
    • Isopropanol, up to 30%
    • Hydrochloric acid, up to 0.1 M
    • Trifluoroacetic acid, up to 10%
    • Formic acid, up to 70%
    Avoid:
    • Oxidizing agents
    • Unfiltered solutions
  • Sample volume
    25 to 500 µL
  • Bed dimensions
    10 x 300
  • Matrix
    Composite of cross-linked agarose
  • pH stability, operational
    3 to 12
  • Theoretical plates
    > 48 000 m-1
DESCRIPTION
Superose™ 6 Increase SEC columns are designed for high-resolution, small-scale preparative purification, and analysis of large globular proteins, protein complexes, and other macromolecules in the molecular weight range Mr~ 5K to ~ 5M. Wide fractionation range: optimized to purify large biomolecules, including membrane proteins, protein complexes, and DNA fragments Very high resolution: small bead size and a narrow particle size distribution provide high resolution, for high protein purity High flow rates: rigid beads give excellent pressure/flow properties Enhanced performance: improved resolution and runtime compared to predecessor “Increase”: Cytiva's new generation of size exclusion chromatography columns Superose™ 6 Increase is a next-generation, agarose-based matrix for size exclusion chromatography. With smaller and more rigid beads than their predecessors, Superose™ 6 Increase columns deliver higher resolution protein purification in shorter runtimes. Fractionation of large proteins and protein complexes Suitable for both preparative and analytical applications, Superose™ 6 Increase SEC columns are the first choice for the characterization of large proteins and protein complexes. They can also be used the study of protein-protein interactions, and as a screening tool to explore the molecular weight distribution of an unknown sample. Superose™ 6 and Superdex™ 200 analysis ranges are complementary Superose™ 6 Increase is designed for separation of protein complexes and other very large molecules, including those with molecular weights exceeding Mr ~400 000. The optimal fractionation range of Superdex™ 200 Increase is complementary, providing higher resolution for proteins with molecular weights below Mr ~400 000. Cleaning-in-place (CIP) capabilities 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 proteins, with minimal risk of carry-over between samples. Regular cleaning can also increase column lifetime. Choose from 3 column sizes to suit varying application needs Column Recommended sample volume Recommended operating flow Efficiency (N/m) Applications Superose™ 6 Increase 3.2/300 4 to 50 µL 0.04 mL/min >48,000 Small-scale preparative purification and analysis of large proteins and other biomolecules, when small sample and buffer consumption is important Superose™ 6 Increase 10/300 GL 25 to 500 µL 0.5 mL/min > 48,000 Standard for small-scale preparative purification and analysis of large proteins and other biomolecules, especially protein complexes Superose™ 6 Increase 5/150 GL 4 to 50 µL 0.3 mL/min > 42,000 Rapid purity check and homogeneity analysis of large proteins and protein complexes Feedback on Superose™ 6 Increase SEC columns "Now I can work on more samples, resulting in higher throughput. I can now purify a protein in 30 minutes instead of an hour." Dr. Tomohiro Nishizawa (Nureki Laboratory). Department of Biological Sciences, Graduate School of Science, The University of Tokyo Successful use in published research Researchers use these pre-packed columns for a variety of applications, such as: Study of a magnetic sensing protein Evaluation of effects two proteins have on microtubule nucleation Production of virus-like particles in E. coli
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