Beckman Coulter CytoFLEX Series Instructions For Use Manual page 281

Flow cytometers
Table of Contents

Advertisement

Table 9.1 Troubleshooting (Continued)
Problem
No data acquisition.
Data populations are
normal on one laser, but
too low on another laser.
B49006AH
Probable Cause
• The threshold setting is too
high.
• The gain setting is too low.
• Sheath fluid flow is
insufficient.
• Laser power is insufficient.
• The sample probe is clogged.
The laser delay setting is
incorrect.
Troubleshooting Table
Corrective Action
1. Decrease the threshold setting. Refer to
Adjusting the Threshold
Data Acquisition and Sample
2. Increase the gain setting. Refer to
Adjusting the Gain
in
CHAPTER 5, Data
Acquisition and Sample
3. Ensure that the sheath fluid harness and/
or waste harness is not kinked.
4. Ensure that the sheath fluid harness and/
or waste harness is securely connected.
5. Run Prime. Refer to
Priming the Flow Cell
in
CHAPTER 11, Replacement/
Adjustment
Procedures.
6. Reinitialize. Refer to
Initializing the
Instrument
in
CHAPTER 3, Daily
7. Restart the Cytometer.
8. Verify that your sample does not have
excessive debris. If it does:
a. Filter the sample using an
appropriately sized mesh aperture
filter.
b. Restain the sample.
9. Clean the sample probe. Refer to
Cleaning the Sample Probe
CHAPTER 10, Cleaning
Procedures.
10. Replace the sample probe and the
sample peristaltic pump tubing. Refer to
Replacing the Sample Probe and/or the
Sample Peristaltic Pump Tubing
CHAPTER 11, Replacement/Adjustment
Procedures.
11. If the problem persists,
1. Ensure that the laser delay is set
correctly. Refer to
Setting Laser Delay
CHAPTER 11, Replacement/Adjustment
Procedures.
2. If the problem persists,
Troubleshooting
9
in
CHAPTER 5,
Analysis.
Analysis.
Startup.
in
in
contact
us.
in
contact us
9-15

Advertisement

Table of Contents
loading

This manual is also suitable for:

CytoflexCytoflex sCytoflex lx

Table of Contents