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Hereditary Thrombotic Risk Panel B |
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The Hereditary Thrombosis Screen B was designed to detect congenital conditions that can cause venous thrombosis. (For patients stabilized on coumadin or not taking coumadin.)
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| Activated Protein C Resistance |
| Antithrombin III Activity |
| Prothrombin Mutation (G20210A) |
| Homocysteine |
Preferred # of Aliquots |
Volume per Aliquot |
Preferred Sample Type |
Processing |
Sample Source |
| 3 |
1mL
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Citrated Plasma |
Frozen |
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| 1 |
5mL
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EDTA Whole Blood |
None |
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