Bio-Rad MicroRotofor™ Cell User Manual

Page 4

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Vacuum source and vacuum trap. (Vacuum in 22–28 mm Hg range)

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Deionized water

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Pipettes (100 µl – 2.75 ml volumes)

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Beaker or equivalent to hold the 3 ml sample volume.

Section 4
Setup and Operation

Note: For a detailed description of the MicroRotofor™ components, the
setup, and analysis of the results, please refer to the MicroRotofor™
instruction manual.

4.1 Overview

•

Prepare the Focusing assembly: Electrode chambers and focusing
chamber with electrode membranes.

•

Prepare and load the starter kit protein sample and seal the loading
ports.

•

Add electrolyte solutions to the electrode chambers.

•

Position the focusing assembly in the chassis and start the IEF run.

•

Stop the run, remove the lid, and connect the system to a vacuum
source.

•

Remove the loading port sealing tape and position the focusing chamber
into the harvesting station.

•

Aspirate the fractions into the harvesting tray.

4.2 Prepare the Focusing Assembly

The focusing assembly consists of the electrode assemblies, the electrode
membranes and the focusing chamber.

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