Sample Preparation

Below you will find guidelines and recommendations concerning sample preparation. Please contact the laboratory if you have supplementary questions.

 

Blood collection tubes

 
  • Serum tubes should be left horizontally for 15-20 minutes at room temperature after collection.

  • Centrifugation.

  • Remove the serum and place in an Eppendorf tube or other suitable container.

  • The patient should be fasting before collection to avoid postprandial lipemia.

  • When collecting samples on Fridays we recommend storing samples in a refrigerator and shipping Sunday/Monday.

 

 

 

 

 

 

Blood smear example

 
  • Please fill the tube correctly to avoid artifacts due to low sample volume. Be sure to mix the blood adequately with the anticoagulant by gentle inversion.

  • Make a fresh blood smear at the time of blood collection and enclose the unstained preparation with the sample tubes. This will ensure an optimal morphological evaluation. 

  • Test results will be most valid if samples are less than 24 hours old when arriving at the laboratory.

 

 

 

 

 

 

Requirements for sample collection and shipment for flow cytometry.

Please contact Vetlab (tel: +45 35 33 29 07) for information and planning of the procedure.

If possible, please include a brief medical history and relevant results from the patient.

The sample must be received by Vetlab within 24 hours of sample collection.
Therefor the sample must be sent the same day it is collected and received the following day at Vetlab. Please be aware of this in connection with the deadline for booking a courier.

It is also possible to use the physical mailbox at Vetlab's entrance (Dyrlægevej 46, 1870 Frederiksberg) after closing hours.

Flow cytometry on blood (if leukemia is suspected):
Submit EDTA tubes and fresh blood smears, preferably unstained and stained.
1-2 ml EDTA blood is often enough, please contact Vetlab if you have any questions. 

Flow cytometry on FNA from lymph nodes (if lymphoma is suspected):
Aspirates from lymph nodes should immediately be placed in a suitable liquid medium.
The liquid medium can either be prepared in the clinic by taking 0.5 ml of EDTA plasma or 0.5 ml of separated serum (preferably from the patient) and placing it in a new 1 ml EDTA tube and adding 0.5 ml of sterile saline (so a total of 1 ml of liquid will be in the new EDTA tube).
Alternatively, PBS (Phosphate buffered saline, pH 7.4) can be used as liquid medium.
Feel free to contact Vetlab if you which to have a few tubes of PBS sent to your clinic for storage.  If the PBS buffer solution is kept refrigerated and handled sterile, it has a long shelf life.
If possible, please also submit FNA on slides from the afflicted lymph node.

It is important to collect many cells, as a high number of cells is required for analysis. Tips for maximizing cellularity in the liquid medium:
The fluid can be withdrawn into the syringe that has been used for FNA and carefully re-injected into the tube to maximize cellularity.
As a guideline, sufficient aspirations should be performed until the fluid acquires a cloudy appearance. 

Feel free to contact Vetlab if you have questions about the collection or shipment.