Acetylcholinesterase and Fetal Hemoglobin, Amniotic Fluid
2006848
Ordering Recommendation
 
Mnemonic
ACETYL AF
Methodology
Qualitative Gel Electrophoresis/Radial Immunodiffusion
Performed
Mon, Wed
Reported
3-11 days  
New York DOH Approval Status
This test is New York DOH approved.
Specimen Required
Patient Preparation
  
Collect
Amniotic Fluid  
Specimen Preparation
Transfer 2 mL amniotic fluid to an ARUP Standard Transport Tube. (Min: 1 mL)  
Storage/Transport Temperature
Ambient.  
Unacceptable Conditions
  
Remarks
Include the Amniotic Fluid AFP and MoM results, if available.  
Stability
Ambient; 2 weeks; Refrigerated: 4 months; Frozen: 3 years  
Reference Interval
Acetylcholinesterase: Negative
Fetal Hemoglobin: Negative  
Interpretive Data
Refer to report

See Compliance Statement B: www.aruplab.com/CS
Statement B: This test was developed and its performance characteristics determined by ARUP Laboratories. The U.S. Food and Drug Administration has not approved or cleared this test; however, FDA clearance or approval is not currently required for clinical use. The results are not intended to be used as the sole means for clinical diagnosis or patient management decisions.
 
Note
 
CPT Code(s)
82013; 83033
Components
Component Test Code*Component Chart Name
2006849Acetylcholinesterase, Amniotic Fluid
2006850Fetal Hemoglobin, Amniotic Fluid
2006853Acetylcholinesterase/Fetal HGB Interp
* Component test codes cannot be used to order tests. The information provided here is not sufficient for interface builds; for a complete test mix, please click the sidebar link to access the Interface Map.
Aliases
  • Acetylcholinesterase Amniotic Fluid AFP
  • Acetylcholinesterase, AF
  • Acetylcholinesterase, Amniotic Fluid
  • AChE-AF
  • Amniotic Fluid, Acetylcholinesterase
  • Fetal Hemoglobin, Amniotic Fluid