Special Instructions
Library of PDFs including pertinent information and forms related to the test
Method Name
A short description of the method used to perform the test
Indirect Immunofluorescence
NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.
No
Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test
Anti-Enterocyte Antibodies
Aliases
Lists additional common names for a test, as an aid in searching
Anti Goblet Cell Ab
Anti-Enterocyte
Specimen Type
Describes the specimen type validated for testing
Serum Red
Specimen Required
Defines the optimal specimen required to perform the test and the preferred volume to complete testing
REQUIRED Completed Anti-Enterocyte Antibody (AEA) Clinical form.
(Testing will not proceed without required form)
Specimen Type: Serum
Container/Tube: Red
Specimen volume: 1 mL
Collection Instructions: Collect blood in a red-top no additive tube and submit 1 mL of serum shipped frozen.
Special Instructions
Library of PDFs including pertinent information and forms related to the test
Forms
Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory
Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected
| Hemolysis | NA |
| Lipemia | NA |
| Icterus | NA |
| Other | NA |
| Specimen Type |
Temperature |
Time |
Special Container |
|
Serum Red |
Frozen |
|
PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information
No
Report Available
The interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.
28 to 56 days
Children's Hospital of Philadelphia
Fees
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.
- Authorized users can sign in to Test Prices for detailed fee information.
- Clients without access to Test Prices can contact Customer Service 24 hours a day, seven days a week.
- Prospective clients should contact their account representative. For assistance, contact Customer Service.
Test Classification
Provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.
These tests were developed and their performance characteristics determined by the Pathology Department at The Children’s Hospital of Philadelphia. They have not been cleared or approved by the U.S. Food And Drug Administration. The FDA has determined that such clearance or approval is not necessary. These tests are used for clinical purposes. It should not be regarded as investigational or for research. This Laboratory is certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA) as qualified to perform high complexity clinical laboratory testing.
| Test Id |
Test Order Name |
Order LOINC Value
|
| FAEAB |
Anti-Enterocyte Antibodies |
Not Provided |
| Result Id |
Test Result Name |
Result LOINC Value
Applies only to results expressed in units of measure originally reported by the performing laboratory. These values do not apply to results that are converted to other units of measure.
|
| Z1700 |
Anti-Enterocyte Antibodies |
Not Provided |
| Z1687 |
Dilution of Serum |
Not Provided |
| Z1688 |
IgG |
Not Provided |
| Z1689 |
IgA |
Not Provided |
| Z1690 |
IgM |
Not Provided |
| Z1691 |
Signed |
Not Provided |
Test Setup Resources
Setup Files
Test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.
Excel |
Pdf
SI Sample Reports
International System (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.
SI Normal Reports |
SI Abnormal Reports