Babesia duncani WA1 IgG IFA
The Babesia duncani WA1 IgG assay is used to detect antibodies due to infection of the tick-borne protozoa Babesia duncani in cases of diagnostic uncertainty or sThe Babesia duncani WA1 IgG assay is used to detect antibodies due to infection of the tick-borne protozoa Babesia duncani in cases of diagnostic uncertainty or suspected chronic infection. The assay is performed by indirect fluorescent antibody (IFA) method. Titer values above the reference intervals are considered evidence of current infection or past infection (e.g. within the last year). uspected chronic infection. The assay is performed by indirect fluorescent antibody (IFA) methods. Titer values above the reference intervals are considered evidence of current infection or past infection (e.g. within the last year).
Human IgG antibody to Babesia duncani (B. duncani) WA1 antigens are detected by an indirect fluorescent antibody (IFA) assay. Briefly, a slide coated with fixed, B. duncani infected red blood cells are incubated with the diluted human serum sample. If specific B. duncani antibodies are present, they remain bound, are then labeled by a fluorescein-labeled antibody conjugate, and then detected by fluorescence microscopy. This test was developed and its performance characteristics were determined by Viracor Eurofins.This test has not been cleared or approved by the U.S. Food and Drug Administration. Results should be used in conjunction with clinical findings, and should not form the sole basis for a diagnosis or treatment decision.
Sera from patients shown to have been infected by the tick-borne pathogens--Babesia microti, Rickettsia rickettsii and Borrelia burgdorferi--were tested and found to be negative by the B. duncani WA1 IgG IFA assay.
1-4 business days from receipt of specimen
|Specimen Type||Order Code||CPT Code||NY Approved||Volume||Assay Range||Special Instructions|
|serum||30290||86753||No||2 mL (min. 0.1mL)||1:256 - 1:1024 titer||
Ship Monday through Friday. Friday shipments must be labeled for Saturday delivery. All specimens must be labeled with patient's name and collection date. A Viracor Eurofins test requisition form must accompany each specimen. Ship specimens FedEx Priority Overnight to: Viracor Eurofins, 1001 NW Technology Dr, Lee's Summit, MO 64086.
Specimens beyond their acceptable length of time from collection as listed in the specimen handling, or specimen types other than those listed.
Specimens are approved for testing in New York only when indicated in the Specimen Information field above.
The CPT codes provided are based on Viracor Eurofins' interpretation of the American Medical Association's Current Procedural Terminology (CPT) codes and are provided for informational purposes only. CPT coding is the sole responsibility of the billing party. Questions regarding coding should be addressed to your local Medicare carrier. Viracor Eurofins assumes no responsibility for billing errors due to reliance on the CPT codes illustrated in this material.