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25675 Allergen, Mushroom, IgE (MUSH)

Allergen, Mushroom, IgE (MUSH)
Test Code: ALMSHSO
Synonyms/Keywords
​Agaricus bisporus, Agaricus hortensis, Buttom Mushroom, Champignon, Common Mushroom, Cultivated Mushroom, Table Mushroom, White Mushroom,
Useful For
​Testing for IgE antibodies may be useful to establish the diagnosis of an allergic disease and to define the allergens responsible for eliciting signs and symptoms.
 
Testing also may be useful to identify allergens which may be responsible for allergic disease and/or anaphylactic episode, to confirm sensitization to particular allergens prior to beginning immunotherapy, and to investigate the specificity of allergic reactions to insect venom allergens, drugs, or chemical allergens.
Specimen Requirements
Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​Serum ​Red Top Tube (RTT) ​Serum Separator Tube (SST) ​0.5 mL for each 5 allergens requested ​For more than 1 allergen: (0.05 mL x number of allergens) + 0.25 mL dead space
Collection Processing Instructions
​Designate specific allergens from the list in Allergens-IgE Antibodies in Special Instructions.
 
Forms: If not ordering electronically, complete, print, and send an Allergen Test Request Form (T236) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/allergen-test-request-form.pdf).
Specimen Stability Information
Specimen Type Temperature Time
​Serum ​ ​Refrigerated (preferred) ​14 days
​Frozen ​90 days
Interference

​Some individuals with clinically insignificant sensitivity to allergens may have measureable levels of IgE antibodies in serum, and results must be interpreted in the clinical context.

False-positive resuts for IgE antibodies may occur in patients with markedly elevated serum IgE (.2,500 kU/L) due to nonspecific binding to allergen solid phases.

Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Mayo Medical Laboratories ​Monday through Friday ​Same day/1 day ​Fluorescence Enzyme Immunoassay (FEIA)
Reference Lab
Test Information
This test was developed and its performance characteristics determined by Marshfield Labs. This laboratory is certified under the Clinical Laboratory Improvement Amendments (CLIA) to perform high complexity testing.
Reference Range Information
Performing Location Reference Range
​Mayo Medical Laboratories
Class
IgE kU/L
Interpretation
0
<0.35
Negative
1
0.35-0.69
Equivocal
2
0.70-3.49
Positive
3
3.50-17.4
Positive
4
17.5-49.9
Strongly positive
5
50.0-99.9
Strongly positive
6
> or =100
Strongly positive
Reference values apply to all ages
Interpretation
​Detection of IgE antibodies in serum (Class 1 or greater) indicates an increased likelihood of allergic disease as opposed to other etiologies and defines the allergens that may be responsible for eliciting signs and symptoms.
 
The level of IgE antibodies in serum varies directly with the concentration of IgE antibodies expressed as a class score or kU/L.
Outreach CPTs
CPT Modifier
(if needed)
Quantity Description Comments
​86003 ​1 ​Allergen specific IgE quan/semiquan each allergen
Classification
This test was developed and its performance characteristics determined by Marshfield Labs. This laboratory is certified under the Clinical Laboratory Improvement Amendments (CLIA) to perform high complexity testing.
Synonyms/Keywords
​Agaricus bisporus, Agaricus hortensis, Buttom Mushroom, Champignon, Common Mushroom, Cultivated Mushroom, Table Mushroom, White Mushroom,
Ordering Applications
Ordering Application Description
If the ordering application you are looking for is not listed, contact your local laboratory for assistance.
Specimen Requirements
Specimen Type Preferred Container/Tube Acceptable Container/Tube Specimen Volume Specimen Minimum Volume
(allows for 1 repeat)
Pediatric Minimum Volume
(no repeat)
​Serum ​Red Top Tube (RTT) ​Serum Separator Tube (SST) ​0.5 mL for each 5 allergens requested ​For more than 1 allergen: (0.05 mL x number of allergens) + 0.25 mL dead space
Collection Processing
​Designate specific allergens from the list in Allergens-IgE Antibodies in Special Instructions.
 
Forms: If not ordering electronically, complete, print, and send an Allergen Test Request Form (T236) with the specimen (http://www.mayomedicallaboratories.com/it-mmfiles/allergen-test-request-form.pdf).
Specimen Stability Information
Specimen Type Temperature Time
​Serum ​ ​Refrigerated (preferred) ​14 days
​Frozen ​90 days
Interference

​Some individuals with clinically insignificant sensitivity to allergens may have measureable levels of IgE antibodies in serum, and results must be interpreted in the clinical context.

False-positive resuts for IgE antibodies may occur in patients with markedly elevated serum IgE (.2,500 kU/L) due to nonspecific binding to allergen solid phases.

Useful For
​Testing for IgE antibodies may be useful to establish the diagnosis of an allergic disease and to define the allergens responsible for eliciting signs and symptoms.
 
Testing also may be useful to identify allergens which may be responsible for allergic disease and/or anaphylactic episode, to confirm sensitization to particular allergens prior to beginning immunotherapy, and to investigate the specificity of allergic reactions to insect venom allergens, drugs, or chemical allergens.
Reference Range Information
Performing Location Reference Range
​Mayo Medical Laboratories
Class
IgE kU/L
Interpretation
0
<0.35
Negative
1
0.35-0.69
Equivocal
2
0.70-3.49
Positive
3
3.50-17.4
Positive
4
17.5-49.9
Strongly positive
5
50.0-99.9
Strongly positive
6
> or =100
Strongly positive
Reference values apply to all ages
Interpretation
​Detection of IgE antibodies in serum (Class 1 or greater) indicates an increased likelihood of allergic disease as opposed to other etiologies and defines the allergens that may be responsible for eliciting signs and symptoms.
 
The level of IgE antibodies in serum varies directly with the concentration of IgE antibodies expressed as a class score or kU/L.
For more information visit:
Performing Laboratory Information
Performing Location Day(s) Test Performed Analytical Time Methodology/Instrumentation
​Mayo Medical Laboratories ​Monday through Friday ​Same day/1 day ​Fluorescence Enzyme Immunoassay (FEIA)
Reference Lab
For billing questions, see Contacts
Outreach CPTs
CPT Modifier
(if needed)
Quantity Description Comments
​86003 ​1 ​Allergen specific IgE quan/semiquan each allergen
Classification
This test was developed and its performance characteristics determined by Marshfield Labs. This laboratory is certified under the Clinical Laboratory Improvement Amendments (CLIA) to perform high complexity testing.
For most current information refer to the Marshfield Laboratory online reference manual.