Please observe that the flowchart below is followed by explanatory text

Step 1
Important: Do not to use EDTA tubes.
Step 2
No obvious handling errors.
Step 3
Step 7 in Instructions for use.
| Potential problem: | Low yield of endothelial precursor cells. |
| Potential cause: | Cells are adhering to the tube. |
| Solution: | Use siliconized tubes according to the instructions. |
Step 8 in Instructions for use.
| Potential problem: | Low yield of endothelial precursor cells. |
| Potential cause: | Poor mixing during incubation with magnetic beads or too intense mixing. |
| Solution: | Ensure that mixing is sufficient to avoid sedimentation but not so intense that the beads fail to bind to the cells. |
Step 4
Step 10 in Instructions to use.
| Potential problem: | False-positive XM-One. |
| Potential cause: | PBS not properly discarded before serum added. |
| Solution: | Make sure that all PBS is discarded according to the Instructions for use. |
Step 5
No obvious handling errors.
Step 6
| Potential problem: | 1. Incorrect setting in flow cytometry, often of the forward-scatter (FSC) and side-scatter (SSC). It is important to adjust the settings so that distinct cell populations can be detected. 2. Wrong cell population obtained. |
| Potential cause: | Poor mixing during incubation with magnetic beads or too intense mixing. |
| Solution: | Experience and handling-knowledge of flow cytometry. Different equipment types require different settings. Settings used for lymphocyte crossmatches can often be used with only minor adjustments. |