What type of specimen is required for a Serum Protein Electrophoresis (SPEP)?

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Last updated: August 23, 2025View editorial policy

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Specimen Requirements for Serum Protein Electrophoresis (SPEP)

Serum Protein Electrophoresis (SPEP) requires a blood sample collected in a serum-separator tube or red-top tube, with 3 mL being the recommended volume for testing. 1

Collection and Handling Requirements

  • Specimen type: Serum (not plasma or whole blood)
  • Collection container: Serum-separator tube or red-top tube
  • Minimum volume: 0.5 mL (though this may be insufficient for repeat testing)
  • Recommended volume: 3 mL
  • Processing: The specimen should be centrifuged with only serum sent for analysis
  • Storage conditions:
    • Up to 1 week when stored refrigerated
    • Indefinite when stored frozen

Shipping and Transport

  • Shipping temperature: Cold pack or frozen preferred; room temperature (20-25°C) is acceptable
  • Delivery timeframe: Overnight delivery recommended
  • Labeling: Patient's name and collection date must appear on specimen label 2

Quality Considerations

  • Grossly hemolyzed, icteric, lipemic, or bacterially contaminated specimens cannot be tested properly and may yield inaccurate results
  • Specimens with less than the recommended volume may be insufficient for repeat testing if needed 2

Clinical Context

SPEP is a critical test in the diagnostic workup of plasma cell disorders, particularly multiple myeloma. The National Comprehensive Cancer Network recommends SPEP as a first-line test for detecting monoclonal proteins (M-proteins) with a sensitivity of approximately 71% 1, 3.

Complementary Testing

For comprehensive evaluation, SPEP should be ordered alongside:

  • Serum immunofixation electrophoresis (SIFE) to characterize any detected protein
  • Serum free light chain (FLC) assay
  • 24-hour urine collection for urine protein electrophoresis (UPEP) and immunofixation (UIFE) 1

Important Considerations

  • Using consistent testing methods for serial monitoring is essential to ensure accurate relative quantification of M-proteins
  • Approximately 3% of multiple myeloma patients have no detectable M-proteins on SPEP (nonsecretory disease), highlighting the importance of complementary testing 2, 1
  • The accuracy and precision of SPEP decrease at lower M-protein concentrations, which may affect monitoring of minimal residual disease 4

By following these specimen collection and handling requirements, clinicians can ensure optimal results from SPEP testing for the diagnosis and monitoring of plasma cell disorders.

References

Guideline

Plasma Cell Disorders Diagnosis and Monitoring

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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