GE28-9909-44
Superdex® 200 Increase 10/300 GL
Cytiva 28-9909-44, column L × I.D. 30 cm × 10 mm, 8.6 μm particle size
Synonym(s):
Superdex Increase
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About This Item
material
glass column
polyethylene filter
product line
Superdex®
form
prepacked column
crosslinking
cross-linked
mol wt
protein Mr 1.3 MDa (exclusion limit)
protein Mr 10-600 kDa (fractionation range)
Mp 1-100 kDa (dextrans fractionation range)
packaging
pkg of 1 ea
manufacturer/tradename
Cytiva 28-9909-44
storage condition
(20% ethanol)
parameter
0.75 mL/min flow rate
1.8 mL/min max. flow rate
25-500 μL sample volume
3.0 Mpa pressure drop required
technique(s)
liquid chromatography (LC): suitable
bed volume
~24 mL
column L × I.D.
30 cm × 10 mm
matrix
cross-linked agarose-dextran composite
matrix active group
dextran-agarose
particle size
8.6 μm
cleaning
1-14
operating pH
3—12
separation technique
size exclusion (SEC)
shipped in
ambient
storage temp.
2-30°C
Related Categories
General description
Superdex™ 200 Increase is a next-generation, dextran-agarose composite matrix for SEC. With smaller and more rigid beads than their predecessors, Superdex™ Increase columns deliver higher resolution purification in shorter run times.
Superdex™ 200 Increase has a selectivity curve optimized for excellent resolution of antibodies and macromolecules within the range Mr ~ 100 000 to ~ 300 000. It is well suited for detection and separation of antibody monomers, dimers, and aggregates present in monoclonal antibody preparations. The outstanding resolving power of this resin facilitates protein characterization, including analysis of antibody size variants, assessment of membrane protein size homogeneity, and the study of protein-protein interactions.
Superdex™ 200 Increase is optimized to give high resolution separation for proteins with molecular weights in the range Mr ~ 100 000 to ~ 300 000. Superose™ 6 Increase provides a complementary fractionation range, resolving very large protein complexes and macromolecules that Superdex 200 Increase cannot separate.
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.
Application
Features and Benefits
- Enhanced performance: improved resolution and runtime compared to predecessor Superdex™ 200.
- Very high resolution: small bead size and narrow particle size distribution provide high resolution, for high protein purity.
- High flow rates: rigid beads give excellent pressure/flow properties.
Preparation Note
Legal Information
Signal Word
Warning
Hazard Statements
Precautionary Statements
Storage Class Code
3 - Flammable liquids
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Articles
This page shows how to perform a purification and homogeneity check of membrane proteins with products from Cytiva.
Understanding pressure drop in chromatography systems is crucial for optimal functionality across different parts of the system.
This page shows Hydrophobic Interaction Chromatography (HIC) in a purification strategy.
This page shows how to perform a purification of His-tagged membrane proteins.
Protocols
Superdex from Cytiva are SEC media consisting of a composite base matrix of dextran and agarose. This page shows how to perform a separation with a superdex column.
This page shows how to refold proteins using gel filtration and products from Cytiva.
Ensure chromatographic sample clarity to avoid column clogging, reduce washing needs, and prolong column life for purification.
This page discusses how to do a purification with SOURCE™ media from Cytiva.
Related Content
Superdex® from Cytiva are Size Exclusion Chromatography media consisting of a composite base matrix of dextran and agarose. This page shows how to perform a separation with a Superdex® column.
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