Used to evaluate patients at risk for rheumatoid arthritis (RA) or those presenting with features of inflammatory arthritis. Rheumatoid factor (RF) IgM antibody may aid in diagnosis and offers higher sensitivity. The Rheumatoid Arthritis Panel is the preferred test for evaluating suspected RA or undifferentiated inflammatory arthritis, whereas the RF Panel is more appropriate for prognostic purposes
Specimen Type: Serum
Collection Tube: Serum separator tube (SST) or red top
Collection Instructions: Separate serum from cells ASAP or within 2 hours of collection. Then transfer available serum to a standard transport tube.
Volume Required: 1 mL with a minimum of 500 mcL
Storage/Transport Temperature: Refrigerated/Frozen
Stability: Ambient (up to 8 Hours), refrigerated (up to 2 weeks/14days), frozen (up to 30 days) and avoid freeze/thaw cycles with no more than 3 in total
Unacceptable Conditions: Contaminated, heat-inactivated, containing clots fibrin or gross red blood cells, or severely lipemic hemolyzed or icteric samples
Normal Human: </=6
This test has been cleared by the US Food and Drug Administration and is used per manufacturer's instructions and per Exsera's SOPs. Performance characteristics were verified by Exsera in a manner consistent with CAP/CLIA requirements.
ELISA or EIA
7 Business Days
Days Performed: M-F
RF IgA, Rheumatoid factor IgA antibodies
RF IgM & RF IgA, Epic Orderable as RF IgM & RF IgA Only