User`s guide

User’s Guide 95
the row number, then press the Delete key on your
keyboard. You can also delete the event using the
Edit/Cut command. Using this command, you could
re-insert the event using the Edit/Paste command if
you wished. To temporarily view the effect of
removing an event without actually removing it from
the table, click the check box adjacent to the event to
de-select it. To re-select the event, click the check box
once again.
6. When you are finished with the Integration Events
table, click the X box to close it and return to your
chromatogram.
Create a Calibration
If you are interested in peak quantitation (calculation of
results based on the running of standards, you must set up
your method for calibration. Further details on how to set up
multiple level calibrations are given in the Method
Development section of this manual. For this tutorial,
however, you will set up a single level of calibration.
Setting up any type of calibration involves the following steps.
• Identify the Calibrated Peaks and enter standard
amounts in the method
• Run the standard sample(s)
• Review the calibration curve
The easiest way to enter calibration peak data is to actually
run the standard sample first, then use the stored data file to
graphically define your calibration peaks. If you have been
following the Tutorial, you should already have a standard
sample saved on your disk. If you do not, you can either run a
standard sample using the steps shown above in the Run a
Preliminary Sample section of this Tutorial, or you may
select one of the data files provided with the data system.
1. Open your stored data file by clicking the Open File
button and select Open Data… Select your standard
data file from the list, or select one of the data files.
Once the file is displayed in your current data
chromatogram window, click the Analyze button to