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GE28-9180-06

PD MultiTrap G-25

Cytiva 28-9180-06

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About This Item

UNSPSC Code:
23151817
NACRES:
NA.56

material

polypropylene and polyethylene

shelf life

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.

feature

wetted part: no

packaging

pkg of 4 ea

manufacturer/tradename

Cytiva 28-9180-06

storage condition

dry media

size

127.8 mm × 85.5 mm × 30.6 mm

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

General description

PD MultiTrap G-25 is designed for high-throughput desalting and buffer exchange of multiple samples. Supplied in packs of 4 plates. Instructions included. Plates can be processed by vacuum or centrifugation. Suitable for manual use as well as for automation together with robotic systems. Sample preparation in the range of 70 to 130 μ without sample dilution. PD MultiTrap G-25 is prepacked with 500 μ Sephadex® G-25 Medium/well. The 96-well plates are manufactured from biocompatible polypropylene. Convenient and fast small-scale cleanup of proteins and other large biomolecules with high reproducibility well-to-well and plate-to-plate. High desalting capacity (>85%) and recovery (70-90%).

Application

Techniques & Applications: DNA and Protein sample preparation. Desalting/Buffer Exchange/Cleanup.

Storage and Stability

Store at 4 to 30 °C (20% Ethanol)
Store at 4 to 30 °C (4 to 8, Used Media 20% Ehtanol or 0.01 M NaOH)

Legal Information

MultiTrap is a trademark of Cytiva
Sephadex is a registered trademark of Cytiva

pictograms

Flame

signalword

Warning

hcodes

Storage Class

3 - Flammable liquids


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

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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.

Protocols

This page shows how to perform sample desalting, buffer exchange and concentration for affinity chromatography of tagged proteins.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service