Synonym(s):
|
Rubella IgG Immunoassay (BioPlex)
|
Requisition
Form
|
G-2A
|
Test
Description
|
The BioPlex is a multiplex system using
Enzyme Immunoassays (EIA) to detect the presence of antibodies associated
with infection or disease to T. gondii,
Rubella and CMV
|
Pre-Approval
Needed
|
N/A
|
Supplemental
Information Required
|
N/A
|
Supplemental
Form(s)
|
N/A
|
Performed on
Specimens from (sources)
|
Human
|
Sample/Specimen
Type for Testing
|
Serum
|
Minimum
Volume/Size Required
|
250 µL
|
Storage/Preservation
Prior to Shipping
|
Serum should be kept at 2°C to 8°C for up
to 7 days or at -20°C or colder for long term storage
|
Transport
Medium
|
N/A
|
Specimen
Labeling
|
-
Two patient-specific identifiers required (e.g., patient full name, date of birth, Medical record number)
- Identifiers on specimen must exactly match submission form.
|
Shipping and
Specimen Handling Requirements
|
- Ship according to Dangerous Goods Regulations,
IATA, and/or CFR 49.
- Handle
as infectious agent using universal precautions.
- Triple
contained in accordance with federal shipping regulations for infectious
agents.
Additional forms & resources
|
Method
|
Multiplex Flow Immunoassay
|
Turn-around
Time
|
4 working days
|
Interferences/Limitations
|
Contaminated,
icteric, lipemic, hemolyzed or heat inactivated sera may cause erroneous
results and should be avoided.
|
Common Causes for
Rejection
|
-
insufficient quantity
- unacceptable specimen type or source
- improper shipping conditions
- expired media or collection container
- discrepancies between specimen label and submission form
- incomplete or missing submission form.
|
Additional Information
|
The Rubella IgG should be considered in conjunction with other laboratory test results as well as the clinical presentation of the patient. Only a physician should interpret the results. |