Last updated on 11-7-2023 by Lee Mbambu Maswaku
Result
- Quantitative (% relative avidity index (% RAI)) and qualitative (high or low avidity)
- This test is performed under accreditation from BELAC, ISO15189.
Purpose of the test
Determination of IgG antibody avidity against rubella virus in serum by ELISA.
Criteria for conducting this test under the reference activities
This test is performed only for samples that are IgM and IgG ELISA positive to rule out a recent infection (< 4-6 weeks ago).
ATTENTION: If you suspect a case of congenital Rubella, please send your sample to the NRC for Congenital Infections
Unacceptable demands
- No clinical indications of Rubella infection.
- Samples that are rubella IgG negative or equivocal.
Instructions for samples
- Type: Serum
- Sample collection: at least 7 days after the onset of the rash
- Storage conditions: Store samples at 4°C before shipment
- Minimum volume: 0.5 ml
Instructions for transportation
Ship in a triple-wrapped package at room temperature.
Turn around time
4 business days
Communication of test results
The result can be communicated via mail, fax, email and eHealth.
Pathogen info
Pathogen(s):
Rubella virus
Accreditation
Is the analysis accredited?
Associated certificate(s):
Materials and methods
Material(s):
Method reference:
SOP 13/3/91/N
Turnaround time and time slots
Turnaround time:
4 days
Request forms
Service in charge of the analysis
Contact person(s)
-
Inge Roukaerts, PhDScientist
Contact email
Analysis categories
Medical