Rabies Antibody, IgG (Vaccine Response)
0099132
Ordering Recommendation
 
Mnemonic
RABIES
Methodology
Semi-Quantitative Enzyme-Linked Immunosorbent Assay
Performed
Tue
Reported
1-8 days  
New York DOH Approval Status
Specimens from New York clients will be sent out to a New York DOH approved laboratory, if possible.
Submit With Order
Specimen Required
Patient Preparation
  
Collect
Serum separator tube.  Also acceptable: lavender (EDTA), green (sodium heparin), Yellow (ACD solution A), or lt. blue (sodium citrate).  
Specimen Preparation
Transfer 0.5 mL serum or plasma to an ARUP Standard Transport Tube. (Min: 0.1 mL)  
Storage/Transport Temperature
Refrigerated.  
Unacceptable Conditions
CSF. Hemolyzed, icteric, or lipemic specimens.  
Remarks
  
Stability
After separation from cells: Ambient: 48 hours; Refrigerated: 2 weeks; Frozen: 1 year  
Reference Interval
0.50 EU/mL or greater: Represents adequate protection against rabies virus following vaccination.  
Interpretive Data


See Compliance Statement B: www.aruplab.com/CS
Statement B: 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.
 
Note
This test is only intended for vaccine response, not for diagnosis of infection.
CPT Code(s)
86790
Components
Component Test Code*Component Chart NameLOINC
0099132Rabies Antibody, IgG (Vaccine Response)58023-3
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
  • Rabies Vaccine