Fig. 5. Run control screen.
3. Insure that the 50 µl sample loop is connected to ports 3 and 6 of the
inject valve. Completely fill the loop with sample protein standard
via port 5 and a syringe and needle.
Do not
remove the syringe from
the injection port after filling the loop or the sample will siphon to
waste.
4. To launch the Run, click on the green
Start
toolbar button. The sample
will be loaded automatically.
5. Clicking the
Hold
toolbar button will hold the gradient pumps at the
current %B value and will not advance the programmed method until
the
Continue
toolbar button is pressed. Clicking the
Pause
toolbar
button will stop the pumps completely. Clicking the
Continue
toolbar
button will re-start the pumps at exactly the point where the program
was paused.
6. When this run is finished, the pumps automatically stop and a run
finished message appears in the bottom right of the status bar.
7. Figure 5 shows a typical run screen and chromatogram for this
separation.
Advance
Frac. Collector
Divert Valve
0.090
0.100
50.0
100% Buffer B
Run Time
Run Volume
0.0 ml
0:24.9
0:00.0
0.00ml/min
0 %B
Gradient Pump: F-10
UV
Conductivity
UV Detector
Set
UV Range
Zero
Baseline
Event
mark
Cond Range
500
Protocol: > 1 0:00.0 Isocratic Flow with 100% Buffer B at 1.00 ml/min for 25.0 min
00:00:00
00:02:00
00:04:00
00:06:00
StepTime Left
Valve Info
0 psi
0.00003 AU
-0.014 mS/cm
Hr:Min:Sec
AU
mS/cm
Collect
Waste
View
Utilities
Options
Edit
Method
New
Method
New
Run
Manual
Setup Protocol
wash
load
1
2
Run
Notes
FullView
Report
PostRun
Log
Help
Grad. Pump
Chart Recorder
1000
High psi
0
Low psi
0.01
0.080
0.070
0.060
0.050
0.040
0.030
0.020
0.010
0.000
-0.010
50.0
0.0
45.0
40.0
35.0
30.0
25.0
20.0
15.0
10.0
5.0
-5.0
Fractions
1
2
3
4
5
6
7
8
9
10
11
12
13
Fraction Vol. Left
SIM1/pH
SIM1/SIG
File
Browser
Conductivity
UV
Window
BioLogic Duo-Flow - Carole Smith - Uno Q1 data - Uno Q1 - Standards
14
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