BIO RAD ZE5, Руководство пользователя

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Chapter 7 Creating Experiments and Workspaces
3. (Optional) To activate all detectors for a particular laser, click All for that laser.
4. (Optional) To clear the entire list of selected fluorophores and active detectors, click Clear All in
the upper right of the Available Detection pane.
5. If necessary, edit the parameter Name to include more descriptive information for each detector,
such as target (for example, CD19).
6. If needed, activate detectors manually.
a. Select the Active checkbox for the detector.
b. Type the name of the detector or fluorophore in the Name box.
7. Click the Next arrow to go to the Samples screen.
Setting Up the Run List
In the Samples screen, you define the run list by specifying how samples are processed. Settings
include media type, well/tube positions, sample names, compensation controls, volume, limit, target
flow rate or target event rate, sampling speed, wash, agitation, temperature, addition of reagent, and
pauses.
Selecting the Media Type
You can select from six predefined media (sample input device) types or create a custom media type.
For more information about media types, see Media Selector on page 69 .
To select the media type
u
In the Media list, do one of the following:
n
To use a standard rack or plate type, click the appropriate button.
n
To create a custom rack or plate type, click Custom, select an existing plate type and click
Select or create a new custom plate, and Click Next.
For more information about creating custom plates, see Creating a Custom Media Type on
page 173 .
170 | ZE5 Cell Analyzer and Everest Software