Table of Contents
Advertisement
TitraLab
®
Programming
sequence
1. Start by programming each method that will be used in the
sequence,
see "Programming method", page
2. If you are using a Sample Changer only:
In the Configuration menu, declare the model of sample changer
used (SAC80, SAC90, SAC850 or SAC950). Depending on the
model of sample changer used, enter the sample changer
configuration parameters.
3. In the Main window, select:
• Working mode = Sequence for manual sample handling.
• or Working mode = SAC Sequence, for automatic
sample handling using a sample changer
4. Press 2 in the Main window.
5. At the line ID, enter a name for the sequence.
6. In a SAC Sequence, for Skip empty position, select
whether you want or not the sample changer to skip to the next
beaker if an empty position is found. If you answer No, 3 options
are offered if an empty position is found: restart the analysis in the
same beaker, skip to the next beaker or end the analysis.
Refer to "Skip empty position", page
7. If you have defined a printer in the Setup > Configuration menu,
select for Print in table, if you want to print all the
sequence results in a table (one line per method) or to print the
results method by method (one frame per method).
8. Press 3 Edit sequence then edit the sequence.
see "Edit sequence menu", page
9. Press 1 Sample stack then edit the sample stack,
stack", page
225.
10. Note that you can start the sequence from a beaker number of
your choice pressing 4 Start from.
See also "Programming TIM sequences", page
See also "Programming SAC sequences", page
TitraLab 870 Reference Manual
180.
Refer to "Sample changer", page
231.
107.
33.
35.
221.
see "Sample
Page 181
Advertisement
Table of Contents
