• Attenuated glass pasteur pipettes
• Sterile PCR Tubes (0.2 ml)*
• Alkaline Lysis Buffer* (store at -20°C; single use aliquots)
• Sterile Rack*
• Mineral Oil*
• Parafilm
• Sterile Gloves
• Mask
• Bonnet

*These materials will be provided by our Centre.


1. Embryo biopsy should be performed in sterile conditions in IVF lab.
2. The fundamental criteria for the selection of the blastomeres should be the presence of a clear nucleus and the maintenance of cell integrity.
3. The biopsy of 2 blastomeres from each embryo is advisable. If the embryo ≤6 cells stage biopsy can be performed for one cell only.
4. Biopsied blastomeres should be manteined in drops of Ca++ Mg++ free biopsy medium, before transferring them into PCR tubes.
5. The biologist performing the transfer of the blastomeres into the PCR tubes must use bonnet, mask and sterile gloves.
6. Attenuated glass Pasteur pipettes with 60-100μm diameter can be used for blastomeres transfer. These pipettes should be prepared before biopsy with a flame source and stored under UV until their use. Commercial pipettes are also available for this purpose. Minimum one pipette for each embryo is necessary.
7. After removal, each blastomere should be washed twice in drops of Ca++ Mg++ free medium, then should be carefully aspirated by using the glass pipette under stereo microscope with 2-3 μl of medium. Afterwards, blastomeres should gently transferred into sterile 0.2 ml PCR tubes, containing 5 µl of alkaline lysis buffer (provided by our Centre), under stereo or phase contrast inverted microscope and overlaid with one drop of PCR mineral oil (provided by our Centre).
IMPORTANT: Blastomeres should be transferred into PCR tubes with as less as possible amount of medium (no more than 2-3μl). An exceeding quantity of medium could determine PCR inhibition.
8. All steps should be double-checked, with a second biologist witnessing the correct labelling of dishes and tubes.
9. The pipettes must be changed after the transfer of blastomeres of each embryo (one pipette for each embryo should be used).
10. Each biopsied blastomere should be transferred into separate PCR tubes. Each tube should be labelled with the number of the embryo and a letter indicating the blastomere (for example, 1A for blastomere A of embryo 1; 1B for blastomere B of embryo 1). Use an indelible pen to label the tubes.
11. Tubes containing 1-2 µl of medium, collected from wash drop of each blastomere and from cell-free wash drop, should added to PCR tubes containing 5 µl of alkaline lysis buffer (provided by our Centre), to be used as negative (blank) controls (one blank per blastomere, and one final medium blank for the whole set). Add to the tubes one drop of PCR mineral oil (provided by our Centre).
12. Spin down the tubes using a microcentrifuge for few seconds and place them in the sterile rack.
13. Seal the rack with parafilm and place it in a safety box or envelope for transportation.
14. Remember to fill the PGD acceptance form

Suggestions for contamination control
Stringent precaution should be taken in order to minimize contamination occurrences. Gloves and dedicated lab coats should be worn during preparation of single cells Preparation of media and reagents should be carried out within a laminar flow cabinet located in a “clean” room restricted to those activity. Mineral oil pipetting should be performed using aerosol-resistant pipette tips and a dedicated pipette for this purpose. 
Gloves should be changed very frequently. Hood surface, and pipetters should be cleaned with chlorine bleach or absolute ethanol and treated with UV light before uses.

• One specimen tube open at a time. 
• Avoid carry-over of lyses buffer to next cell. If cell lyses, change pipet tips and biopsy a second cell in a separate tube labeled accordingly. 
• Do not use oil. 
• No stage warmer. 
• Limit the number of embryos biopsied at one time to 5 to prevent evaporation of placement droplet and wash droplet. 
• Limit the transfer of media into wash droplet. 
• Keep the sample tubes in an upright orientation holds the DNA in a set position through shipping for accurate DNA isolation. 

• Check tube labels are readable before packing tubes. 
• Include original informed consent forms (yours and ours). 
• Include embryo biopsy worksheet. 
• Keep a supply of cold shipping packets and Styrofoam containers that come with reagents. 
• Avoid dry ice. 
• The day before biopsy, request courier pickup an hour after expected completion time. 
• Fax biopsy data worksheet ahead of shipment. 
• Attach airline security letter on your letterhead to outside of box. 

Download guidelines!