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HelpTest ID BLOD0198 Prostatic Acid Phosphatase, Serum
Useful For
Aiding in predicting recurrence after radical prostatectomy for clinically localized prostate cancer
Following response to androgen ablation therapy, when used in conjunction with prostate-specific antigen
Specimen Type
SerumSpecimen Required
Patient Preparation: For 12 hours before specimen collection, patient should not take multivitamins or dietary supplements (eg, hair, skin, and nail supplements) containing biotin (vitamin B7).
Collection Container/Tube:
Preferred: Red top
Acceptable: Serum gel
Submission Container/Tube: Plastic vial
Specimen Volume: 1 mL
Collection Instructions: Centrifuge and aliquot serum into a plastic vial.
Specimen Minimum Volume
0.4 mL
Reject Due To
| Gross hemolysis | Reject |
| Gross lipemia | OK |
Specimen Stability Information
| Specimen Type | Temperature | Time |
|---|---|---|
| Serum | Refrigerated (preferred) | 7 days |
| Frozen | 180 days |
Day(s) Performed
Monday, Wednesday, Friday
Method Name
Automated Chemiluminescent Immunometric Assay
Performing Laboratory
Mayo Clinic Laboratories in Rochester
CPT Code Information
84066
Secondary ID
8019Reporting Name
Prostatic Acid Phosphatase, SReference Values
≤2.1 ng/mL
Test Classification
This test has been cleared, approved, or is exempt by the US Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.Report Available
1 to 3 days
Sanford Laboratories - Bismarck Additional Information:
SANFORD LABORATORY INTERFACE BUILD INFORMATION
| Result Code | Result Code Description |
|---|---|
| 3340 | Prostatic Acid Phosphatase |