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Managed by:
Michelle Stepp

Laboratory Customer Service Coordinator

Email:
michelle.stepp@bassett.org

Phone:
607-547-3866
607-547-6722
Fax:
607-547-5438

Created by:

Benjamin Bascomb & Jamie Govern (2015)

____________________________________

 

Informational Links

Lab Departments

Lab Specific Documents

Informational Links for Providers

 

Patient Information

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General Information

Top Reference Laboratory (In order to search)

  1. Mayo Clinical Labs
  2. ARUP Laboratories
  3. Quest Laboratories
  4. LabCorp

Mayo Clinic Laboratories

Epic Test Code LAB3821 5'Nucleotidase

Additional Codes

MML Code: F5NUL

 

Performing Laboratory

ARUP Laboratories

NY State Approved

Yes

Reporting Name

5' Nucleotidase

Method Name

Quantitative Enzymatic

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Refrigerated (preferred) 7 days
  Frozen  14 days
  Ambient  4 hours

Specimen Required


Specimen Required


Specimen Type: Serum

Container/Tube: SST or Red

Specimen Volume: 1 mL

Collection Instructions: Draw blood in a serum gel tube(s), plain red-top tube(s) is acceptable. Spin down and send 1 mL of serum refrigerate in a plastic vial.


Bassett Healthcare Network Clinical Laboratories Note:

Blood Tube Draw Volume
Min 50% draw volume  

  • 50% of the tube fill volume is required for proper blood to additive ratio.

Specimen Type

Serum

Specimen Minimum Volume

0.5 mL

Reference Values

0 - 15 U/L

 

Report Available

1 to 6 days

Day(s) Performed

Sunday through Saturday

Reject Due To

Hemolysis: Mild; reject, Gross; reject
Thawing: Warm reject; Cold OK
Lipemia: NA
Icterus: NA
Other: NA

CPT Code Information

83915

LOINC Code Information

Test ID Test Order Name Order LOINC Value
F5NUL 5' Nucleotidase 1690-7

 

Result ID Test Result Name Result LOINC Value
Z2607 5' Nucleotidase 1690-7

Secondary ID

57285

Test Classification

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.