Aid in the diagnosis of lymphocytic choriomeningitis (LCM) viral infection.
Semi-Quantitative Indirect Fluorescent Antibody
Serum separator tube.
Separate serum from cells ASAP or within 2 hours of collection. Transfer 1 mL serum to an ARUP Standard Transport Tube. (Min 0.2 mL) Parallel testing is preferred and convalescent specimens must be received within 30 days from receipt of the acute specimens. Mark specimens plainly as "acute" or "convalescent."
Contaminated, hemolyzed, or severely lipemic specimens.
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year (avoid repeated freeze/thaw cycles)
|2001633||Lymphocytic Choriomeningitis (LCM) Virus Antibody, IgG||< 1:10 Negative - No significant level of LCM virus IgG antibody detected.
≥ 1:10 Positive - Presence of IgG antibody to LCM virus detected, suggestive of current or past infection.
|2001634||Lymphocytic Choriomeningitis (LCM) Virus Antibody, IgM||< 1:10 Negative - No significant level of LCM virus IgM antibody detected.
≥ 1:10 Positive - Presence of IgM antibody to LCM virus detected, suggestive of current or past infection.
The best evidence for current infection is a significant change on two appropriately timed specimens, where both tests are done in the same laboratory at the same time.
Compliance Statement D: For laboratory tests using a manufactured RUO kit. This test was developed and its performance characteristics determined by ARUP Laboratories. The U. S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
|Component Test Code*||Component Chart Name||LOINC|
|2001636||LCM Virus Ab, IgG||9765-9|
|2001637||LCM Virus Ab, IgM||9767-5|
- LCM Antibodies, Serum