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feature
wetted part: no
packaging
pkg of 1 ea
manufacturer/tradename
Cytiva 28-9180-04
storage condition
dry media
matrix
cross-linked dextran
particle size
>50 μm (dry), 85-260 μm
cleaning
2-13
working range
2-13
suitability
suitable for bioprocess medium
Related Categories
1 of 4
This Item | GE28-9180-07 | GE28-9180-08 | GE27-5325-01 |
|---|---|---|---|
| matrix cross-linked dextran | matrix cross-linked dextran | matrix cross-linked dextran | matrix - |
| particle size >50 μm (dry), 85-260 μm | particle size >50 μm (dry), 85-260 μm | particle size >50 μm (dry), 85-260 μm | particle size 20-80 μm (dry) |
| feature wetted part: no | feature wetted part: no | feature wetted part: no | feature - |
| packaging pkg of 1 ea | packaging pkg of 50 ea (columns) | packaging pkg of 50 ea (columns) | packaging pkg of 50 columns |
| manufacturer/tradename Cytiva 28-9180-04 | manufacturer/tradename Cytiva 28-9180-07 | manufacturer/tradename Cytiva 28-9180-08 | manufacturer/tradename Cytiva 27-5325-01 |
| storage condition dry media | storage condition dry media | storage condition dry media | storage condition - |
General description
Application
Features and Benefits
- Convenient and fast small-scale cleanup of proteins and other large biomolecules (>5000 Mr) with the possibility to run multiple samples in parallel.
- Range of applications such as desalting, buffer exchange, and removal of low-molecular weight compounds.
- High desalting capacity.
- Reproducible, high throughput, parallel cleanup of protein samples.
- Sample preparation in the range of 100 to 180 μl without sample dilution.
Preparation Note
Legal Information
Storage Class
12 - Non Combustible Liquids
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Articles
Desalting at laboratory scale is a well-proven, simple, and fast method that will rapidly remove low molecular weight contaminants at the same time as transferring the sample into the desired buffer in a single step.
This page shows how to purify GST-tagged proteins using GST SpinTrap™ from Cytiva.
Protocols
This page shows how to perform sample desalting, buffer exchange and concentration for affinity chromatography of tagged proteins.
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