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Maternal Cell Contamination Study, STR Analysis
Test Code15896
CPT Codes
81265
Preferred Specimen
5 mL whole blood collected in an EDTA (lavender-top) tube
Minimum Volume
3 mL
Instructions
This code is only to be used when ordering code 15816, Sickle Cell Anemia, DNA Probe Analysis, Fetus, referred to Quest Diagnostics Nichols Institute, San Juan Capistrano. This test must be performed in order to rule out maternal contamination of the fetal sample.
This test is run in conjunction with a fetal specimen (Amniotic fluid or CVS). The assay cannot be run until fetal cultures are ready. The TAT is therefore dependent on the TAT of the fetal DNA test on the same patient.
This test is run in conjunction with a fetal specimen (Amniotic fluid or CVS). The assay cannot be run until fetal cultures are ready. The TAT is therefore dependent on the TAT of the fetal DNA test on the same patient.
Transport Temperature
Room temperature
Specimen Stability
Room temperature: 8 days
Refrigerated: 8 days
Frozen: unacceptable
Refrigerated: 8 days
Frozen: unacceptable
Methodology
Multiplex Polymerase Chain Reaction • Fragment Analysis by Capillary Electrophoresis
FDA Status
This test was performed using a kit that has not been cleared or approved by the FDA. The analytical performance characteristics of this test have been determined by Quest Diagnostics. This test should not be used for diagnosis without confirmation by other medically established means.
Setup Schedule
See instructions
Reference Range
See Laboratory Report
Clinical Significance
Maternal Cell Contamination Study, STR Analysis, provides assurance that test results from fetal specimens are not influenced by contaminating maternal material. This test also allows for establishing the proper maternal-fetal relationship between specimens by using sophisticated analysis of 15 highly polymorphic STR loci.