- Leica trinocular S8 Apo Microscope
- Motic Trinocular Stereo zoom Microscope
- Inverted microscope
- Nikon TMD inverted Microscope
- Olympus IX51 Inverted microscope
- Olympus IX71 Inverted microscope
- Olympus IX53 Inverted microscope
- Centrifuge Machines
- Select c5 centrifuge
- Sperm Counting Chambers
- Mackler Sperm Counting Chambers
Searching Box
Products
Embryo Culture
- MINC Benchtop Incubator
- Gamete Buffer
- Sperm Medium
- Sperm Gradient Kits
- Spermient®
- Sperm Cryopreservation Buffer
- Follicle Flush Buffer
- Oocyte Freeze Kit
- Oocyte Thaw Kit
- Fertilization Medium
- Culture Oil
- Hyaluronidase
- PVP
- Cleavage Medium
- Cryopreservation Kit
- Embryo Biopsy Medium
- Thawing Kit
- Blastocyst Medium
- Blastocyst Cryopreservation Kit
- Blastocyst Thawing Kit
- Blastocyst Vitrification Kit
- Blastocyst Warming Kit
Ovum Collection
Intrauterine Insemination (IUI)
Gamete/Zygote Intra-Fallopian Transfer (G.I.F.T) (Z.I.F.T)
Embryo Transfer
Follicular Volume & Aspiration
It is important to consider the volume of follicular fluid in relation to the dead space in the ovum aspiration needle and aspiration line. To minimize trauma to the oocyte-cumulus complex, it is suggested that a continuous column of fluid within the aspiration needle be maintained. This helps prevent the oocyte-cumulus complex from sticking to the wall of the needle or aspiration line. In addition, air will travel faster than fluid through the aspiration lumen, and if air is introduced when oocytes are present within the needle, it is possible that the oocyte may be damaged. As a consequence, ovum aspiration technique should aim to minimize the introduction of air into the needle during aspiration.