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26644 Ladybeetle Multicolored Asian (Harmonia axyridis) IgE (FLBAE)

Ladybeetle Multicolored Asian (Harmonia axyridis) IgE (FLBAE)
Test Code: FLBAESO
Synonyms/Keywords

​​Harmonia axyridis, Ladybeetle Multicolored Asian, Lady Asian Beetle ​

Test Components

​Measurement of Ladybeetle Asian IgE along with class and interpretation.

Useful For

​This assay is used to detect allergen specific-IgE using an enzyme immunoassay (EIA). In vitro allergy testing is the primary testing mode for allergy diagnosis.

Specimen Requirements
Specimen TypePreferred Container/TubeAcceptable Container/TubeSpecimen VolumeSpecimen Minimum Volume
(allows for 1 repeat)		Pediatric Minimum Volume
(no repeat)
​Serum
​Red Top Tube(RTT)
​Serum Separator Tube (SST)
​​0.5 mL
​0.5 mL
​
Collection Processing Instructions

​Draw blood in a plain red-top tube(s), serum separator gel tube(s) (SST) is acceptable. Centrifuge and send 0.5 mL of serum refrigerated in a plastic vial.

Send to Mayo who refers testing to Eurofins Viracor.​​

Specimen Stability Information
Specimen TypeTemperatureTime



​​Serum​
​
​

​Refrigerated (preferred)
​28 days
​Frozen
​365 days
​Ambient
​28 days
Rejection Criteria

Gross Lipemia

Performing Laboratory Information
Performing LocationDay(s) Test PerformedAnalytical TimeMethodology/Instrumentation

Mayo Clinic Laboratories
forwards testing to Eurofins Viracor​
​​Monday through Friday
​2 to 7 days
​Enzyme Immunoassay (EIA)
Reference Lab
Mayo Clinic Laboratories
Test Information

​The conventional EIA uses allergen-coated discs from several suppliers and an enzyme-labeled anti-IgE.

​This test was developed and its performance characteristics determined by Eurofins Viracor.  It has not been cleared or approved by the US Food and Drug Administration.  

Reference Range Information

< 0.35 kU/L

Interpretation

​

ClassIgE (kU/L)Comment
0
<0.35Below Detection
10.35-0.69Low Positive
20.70-3.49Moderate Positive
33.50-17.49Positive
417.50-49.99Strong Positive
5>=50Very Strong Positive


Outreach CPTs
CPTModifier
(if needed)		QuantityDescriptionComments

​86003
​​​1
​​
Classification
This test was developed and its performance characteristics determined by Eurofins Viracor.  It has not been cleared or approved by the US Food and Drug Administration.  This test is used for clinical purposes.  It should not be regarded as investigational or for research.
Synonyms/Keywords

​​Harmonia axyridis, Ladybeetle Multicolored Asian, Lady Asian Beetle ​

Test Components

​Measurement of Ladybeetle Asian IgE along with class and interpretation.

Ordering Applications
Ordering ApplicationDescription

​Cerner
​Ladybeetle Multicolored Asian (Harmonia axyridis) IgE (FLBAE)
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Specimen TypePreferred Container/TubeAcceptable Container/TubeSpecimen VolumeSpecimen Minimum Volume
(allows for 1 repeat)		Pediatric Minimum Volume
(no repeat)
​Serum
​Red Top Tube(RTT)
​Serum Separator Tube (SST)
​​0.5 mL
​0.5 mL
​
Collection Processing

​Draw blood in a plain red-top tube(s), serum separator gel tube(s) (SST) is acceptable. Centrifuge and send 0.5 mL of serum refrigerated in a plastic vial.

Send to Mayo who refers testing to Eurofins Viracor.​​

Specimen Stability Information
Specimen TypeTemperatureTime



​​Serum​
​
​

​Refrigerated (preferred)
​28 days
​Frozen
​365 days
​Ambient
​28 days
Rejection Criteria

Gross Lipemia

Useful For

​This assay is used to detect allergen specific-IgE using an enzyme immunoassay (EIA). In vitro allergy testing is the primary testing mode for allergy diagnosis.

Test Components

​Measurement of Ladybeetle Asian IgE along with class and interpretation.

Reference Range Information

< 0.35 kU/L

Interpretation

​

ClassIgE (kU/L)Comment
0
<0.35Below Detection
10.35-0.69Low Positive
20.70-3.49Moderate Positive
33.50-17.49Positive
417.50-49.99Strong Positive
5>=50Very Strong Positive


For more information visit:
Performing Laboratory Information
Performing LocationDay(s) Test PerformedAnalytical TimeMethodology/Instrumentation

Mayo Clinic Laboratories
forwards testing to Eurofins Viracor​
​​Monday through Friday
​2 to 7 days
​Enzyme Immunoassay (EIA)
Reference Lab
Mayo Clinic Laboratories
For billing questions, see Contacts
Outreach CPTs
CPTModifier
(if needed)		QuantityDescriptionComments

​86003
​​​1
​​
Classification
This test was developed and its performance characteristics determined by Eurofins Viracor.  It has not been cleared or approved by the US Food and Drug Administration.  This test is used for clinical purposes.  It should not be regarded as investigational or for research.
For most current information refer to the Marshfield Laboratory online reference manual.