Measles IgM

Laboratory Fee Schedule
Procedure #: MCW0328A    
CPT:86765

Synonym(s):antibodies, capture enzyme immunoassay, rubeola, serum, serology
Requisition FormG-2A
Test DescriptionAn IgM capture enzyme-linked Immunosorbent assay (ELISA) to detect the presence of IgM antibodies to measles virus in patients suspected of being infected with the measles virus.
Pre-Approval NeededN/A
Supplemental Information RequiredN/A
Supplemental Form(s)N/A
Performed on Specimens from (sources)Human
Sample/Specimen Type for TestingSerum  
Minimum Volume/Size Required1.0 mL
Storage/Preservation Prior to Shipping
  • Store specimens at 2°C to 8°C for up to 4 days.
  • For storage longer than 4 days, store frozen at -20°C or colder
  • Never freeze serum in serum separator tubes.
Transport MediumN/A
Specimen Labeling
  • At least two patient-specific identifiers required on specimen (e.g., patient full name, date of birth, medical record number).
  • Three unique patient identifiers are preferred.
  • Patient identifiers on specimen label must exactly match identifiers on submission form. (e.g. abbreviated name on label and full name on form is not acceptable.)
  • Additional DSHS Laboratory specimen labeling guidelines available online here.
Shipping and Specimen Handling Requirements
  • Ship according to Dangerous Goods Regulations, IATA, and/or CFR 49.
  • Category B Biological Substance, UN3373 shipping requirements apply.
  • Submitters are responsible for packaging and shipping specimens according to regulatory requirements.
  • Additional DSHS Laboratory specimen shipping guidelines online here.
  • Ship overnight on cold packs if specimen will arrive at the Lab within 4 days of collection.
  • Ship overnight on dry ice if specimen will arrive at the Laboratory more than 4 days after time of collection
MethodIgM capture ELISA
Turn-around Time2 business days
Interferences/LimitationsThe absence of detectable IgM antibodies does not rule out the possibility of recent or current infection.
Common Causes for Rejection
  • insufficient specimen volume
  • unacceptable specimen type or source
  • improper storage or shipping conditions
  • expired media or collection container used
  • discrepancies between specimen label and submission form
  • Incomplete or missing submission form
Additional Information
  • Results must always be interpreted together with other clinical and diagnostic data