ALDP - Performance: Autoimmune Liver Disease Panel, Serum

Test Catalog

Test Name

Test ID: ALDP    
Autoimmune Liver Disease Panel, Serum

Method Description Describes how the test is performed and provides a method-specific reference

Smooth muscle antibodies (SMA):

The patient's serum in 1:20 and 1:40 dilutions is added to a tissue substrate of mouse stomach/kidney and incubated. Fluorescein-conjugated antiglobulin is then added. The slides are read with a fluorescence microscope.(Doniach D, Roitt IM, Walker JG, Sherlock S: Tissue antibodies in primary biliary cirrhosis, active chronic [lupoid] hepatitis, cryptogenic cirrhosis, and other liver diseases and their clinical implications. Clin Exp Immunol 1966 July;1[3]:237-262)


Anti-mitochondrial antibodies (AMA):

Enzyme immunosorbent assay with purified M2 antigens. This method detects both IgG and IgM antibodies to M2 antigens.(Package insert: Axis-Shield Diagnostics Limited, United Kingdom, August 2000)


Antinuclear antibodies (ANA2):

The method used to detect antinuclear antibody (ANA) is enzyme-linked immunosorbent assay (ELISA). A HEp-2 lysate supplemented with various purified antigens (double-stranded deoxyribonucleic acid (dsDNA), histone, SS-A (Ro), SS-B (La) Smith, RNP, Scl-70, Jo-1, plus centromere antigen) are coated onto microtiter plate wells. A dilution of patient serum is added to the well and incubated. After washing to remove unbound serum protein, an enzyme conjugated antihuman IgG antibody is added to detect human IgG bound to the microtiter plate well. After incubation and washing to remove unbound conjugate, a substrate to the enzyme is added to the well. After incubation, the enzyme substrate reaction is stopped. The complete assay is measured on a spectrophotometer plate reader. The optical density measured is proportional to the antibody present in the patient serum. Testing is performed on the Triturus instrument by Grifols.(Package insert: ELISA kits, Bio-Rad Laboratories, Hercules CA)

PDF Report Indicates whether the report includes an additional document with charts, images or other enriched information


Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.

Monday through Friday; 9 a.m. and 4 p.m., Saturday; 12 p.m.

Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.

2 days

Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result

3 days

Specimen Retention Time Outlines the length of time after testing that a specimen is kept in the laboratory before it is discarded

7 days

Performing Laboratory Location The location of the laboratory that performs the test