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GE28-9909-44

Sigma-Aldrich

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

UNSPSC Code:
41115700
NACRES:
SB.52
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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 size exclusion chromatography columns are well suited for high-resolution analysis and small-scale purification of monoclonal antibodies (mAb) and other biomolecules with Mr~ 10 000 to ~ 600 000.

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

For both preparative and analytical purposes
Gel filtration for small-scale (25-500 mL) preparative purification.
Long term use: all commonly used aqueous buffers, up to 8 M urea, ionic and non-ionic detergents, up to 6M guanidine hydrochloride

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

Storage Temp.: 4°C to 30°C
Please be aware this product may be shipped 90 days before the expiration date. For more information on the batch specific expiration date, please contact technical service.
Store at 4 to 30 °C (20% Ethanol)

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

Superdex is a registered trademark of Cytiva

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Storage Class Code

3 - Flammable liquids


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Articles

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Protocols

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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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