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This test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the U.S. Food and Drug Administration.
|Test ID||Test Order Name||Order LOINC Code|
|LPMAF||Lymphocyte Proliferation Panel for Mitogens and Antigens||In Process|
|Result ID||Test Result Name||Result LOINC Code|
|32326||Viab of Lymphs at Day 0||In Process|
|32318||Viab of Lymphs at Day 0||In Process|
|32327||Max Prolif of CA as % CD45||69014-9|
|32321||Max Prolif of PWM as % CD45||69019-8|
|32322||Max Prolif of PWM as % CD3||69020-6|
|32328||Max Prolif of CA as % CD3||69015-6|
|32329||Max Prolif of TT as % CD45||69016-4|
|32323||Max Prolif of PWM as % CD19||69037-0|
|32319||Max Prolif of PHA as % CD45||69038-8|
|32330||Max Prolif of TT as % CD3||69029-7|
|32320||Max Prolif of PHA as % CD3||57741-1|
LOINC and CPT codes are provided by the performing laboratory.