Acetylcholinesterase and Fetal Hemoglobin, Amniotic Fluid
Use following an abnormal amniotic fluid alpha fetoprotein (AFP) result to evaluate possibility of a fetal open neural tube defect.
Qualitative Gel Electrophoresis/Radial Immunodiffusion
New York DOH Approval Status
Transfer 2 mL amniotic fluid to an ARUP Standard Transport Tube. (Min: 1 mL)
Include the Amniotic Fluid AFP and MoM results, if available.
Ambient: 2 months; Refrigerated: 4 months; Frozen: 3 years
Fetal Hemoglobin: Negative
Refer to report
This test was developed and its performance characteristics determined by ARUP Laboratories. It has not been cleared or approved by the US Food and Drug Administration. This test was performed in a CLIA certified laboratory and is intended for clinical purposes.
Laboratory Developed Test (LDT)
|Component Test Code*||Component Chart Name||LOINC|
|2006849||Acetylcholinesterase, Amniotic Fluid||30106-9|
|2006850||Fetal Hemoglobin, Amniotic Fluid||28067-7|
|2006853||Acetylcholinesterase/Fetal HGB Interp||48767-8|
- Acetylcholinesterase Amniotic Fluid AFP
- Acetylcholinesterase, AF
- Acetylcholinesterase, Amniotic Fluid
- Amniotic Fluid, Acetylcholinesterase
- Fetal Hemoglobin, Amniotic Fluid