Bio-Rad MicroRotofor™ Cell User Manual

Page 4

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

Deionized water

Pipettes (100 µl – 2.75 ml volumes)

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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