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Back to Test Catalogue
Test ID: NFLC SP

Neurofilament Light Chain (NfL), Serum/Plasma (Test Site St. Michael’s Hospital)

Test Overview

Method

Electrochemiluminescent immunoassay (ECLIA)

Analytical Platform

Roche

Result Included

Neurofilament Light Chain

Specimen

Specimen Type

Serum
Plasma (Li heparin)


Important Note: TEST ID NFLC SP
Non-interfaced clients should specify the Test ID TEST ID NFLC SP when ordering this test. Not doing so will cause processing delays while ICL ascertains which test you are requesting.
Similar testing is available for clinical use at The Ottawa Hospital: Neurofilament Light Chain (NfL), Serum/Plasma

Containers

Preferred Containers

Gold top (clot activator & gel)

Acceptable Containers

Green top (lithium heparin)

Volume

Sample Volume

1.0 mL

Minimum Volume

0.4 mL

Patient Preparation

High dose biotin supplementation may interfere with analysis – patients should stop biotin consumption at least 72 hours prior to the collection of a sample.

Collection & Handling

Handling Information

Store and send frozen.

Stability

Ambient Refrigerated Frozen
1 day 14 days 3 years

Stable up to 3 freeze-thaw cycles.

Performance & Interpretation

Turnaround Time

8 days

Results

Name
Units
Reference Range
Conversion
  1. Neurofilament Light Chain
    pg/mL

    Comment

    Serum NfL levels in healthy individuals are about 2.5% of the levels in CSF and correlate highly with the concentrations in CSF.

Referral Location

Canada

Interface & Setup

HL7 Interface Codes

Order Code Result Name Result Codes Units
NFLC SP Neurofilament Light Chain 65355 pg/mL

Test Version

Last Updated

2025-07-30