Test Code 8NKCL Flow Cytometry - NK-CLPD Panel
Laboratory Code
LAB5234
Specimen Requirements
Submit one of the following:
Fresh specimen required
(a) Specimen Type: Bone Marrow
Container/Tube: Lavender Top (EDTA), Green Top (Sodium Heparin)
Preferred Volume: 2.0 mL
(b) Specimen Type: Peripheral Blood
Container/Tube: Lavender Top (EDTA), Green Top (Sodium Heparin)
Preferred Volume: 3.0 mL
Collection Instructions: Collect 5.0 - 6.0 mL blood if WBC < 5 x 109/L.
(c) Specimen Type: Lymph Node / Solid Tumour
Container/Tube: Sterile container with 5.0 mL RPMI 1640 media
Preferred Volume: 5 mm(3) or larger biopsy
Collection Instructions: Place tissue directly into 5.0 mL RPMI 1640 media after biopsy.
Do not leave tissue to air-dry or fix tissue in formalin.
(Prearrange with Flow Cytometry Laboratory for transport media prior sample collection)
(d) Specimen Type: Body Fluid
Container/Tube: Sterile tube with 0.6 mL transfix media
Preferred Volume: 3.0 - 6.0 mL
(Prearrange with Flow Cytometry Laboratory for transport media prior sample collection)
Additional Collection Instructions: All specimens should be shipped to the lab in ambient temperature (18 - 25oC) within 24 - 48 hrs of collection. Specimen received after 48 hrs of collection will nonetheless be processed but results may be compromised. For overseas specimens, avoid shipping on Friday or eve of public holidays.
Specimen Stability
Fresh specimen required
Ambient | 24 hours (preferred) |
---|---|
Refrigerate | 48 hours |
Methodology
Flow Cytometry
Days and Times Performed
Monday through Friday. TAT 14 - 16 days (STAT 7 - 9 days)
Reference Interval
See laboratory report
Testing Laboratory
National University Hospital
Flow Cytometry, 67724016
Useful For
The extended NK-cell panel is to characterize neoplastic NK-cell populations. The specific immunophenotype can be used for subsequent MRD monitoring. Clinical indication: to diagnose NK-cell neoplasms
Service Code
12660
Update
Last updated 08/01/2025
Test Info
Pre-arrange with Haematology before ordering the test.
This laboratory test has undergone in-house evaluation with appropriate quality assurance and control measures in line with laboratory best practice and accreditation requirements.
Reagent(s) used in this test is/are ordered through HSA’s Special Access Route, which provides interim access without full registration.
Unacceptable Condition
Specimen Type | |
---|---|
Bone Marrow/Peripheral Blood/Body Fluid | Frozen |
Lymph Node/Solid Tumour/Other Tissues | Frozen or air-dry or formalin fixed tissues |