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The following protocols and tips are for the vitrification of embryos from 2PN (two-pronuclear zygote) to blastocyst using our Vitrification Freeze Kit, Cryolock or CryoTip or HSV Security Vitrification Straws.
ALL PROCEDURES MUST BE PERFORMED AT ROOM TEMPERATURE (22 - 27°C).
Note: Prior to vitrification of blastocysts, refer to Collapsing Protocol, Human Blastocysts.
Have all necessary materials, tools and equipment ready and easily accessible before starting procedure.
As an added precaution during the preparation procedure, carefully examine each CryoTip outside of the package. Prior to use, all CryoTips should be examined under a suitable magnification (40x power) for possible damage (such as tip breakages or cracks) that may have occurred during transport.
As an added precaution during the preparation procedure, carefully examine each CryoTip outside of the package. Prior to use, all CryoTips should be examined under a suitable magnification (40x power) for possible damage (such as tip breakages or cracks) that may have occurred during transport.
1. Aseptically dispense one (1) 50 μL drop of ES.
2. Transfer embryo(s) (2 maximum), to the ES drop and expose undisturbed for 6-10 minutes.
NOTE: The specimen(s) will shrink and then gradually return to original size, indicating that equilibration is complete.
3. During above equilibration in ES, aseptically dispense one (1) 50 μL drop of VS 2 minutes prior to complete equilibration.
4. Transfer embryo(s) with minimal volume of medium from ES to the VS drop for 30 seconds before loading.
5. Gently pipette embryo(s) once within VS drop to ensure complete rinse with VS.
NOTE: To minimize floating, after 10 seconds pipette the specimen(s) to the bottom center of the VS drop.
6. Load, seal and plunge CryoTip into LN2 within 80 seconds, not to exceed 110 seconds after initial exposure to VS.
7. Refer to CryoTip Loading Protocol diagram and product insert for detailed loading instructions.
1. Aseptically dispense one (1) 50 μL drop of ES.
2. Transfer embryo(s) (2 maximum), to theES drop and expose undisturbed for 6-10 minutes.
NOTE: The specimen(s) will shrink and then gradually return to original size, indicating that equilibration is complete.
3. During above equilibration in ES, aseptically dispense one (1) 50 μL drop of VS 2 minutes prior to complete equilibration.
4. Transfer embryo(s) with minimal volume of medium from ES drop to the VS drop for 30 seconds before loading.
5. Gently pipette embryo(s) at least once within VS drop to ensure complete rinse with VS.
NOTE: To minimize floating, after 10 seconds pipette the specimen(s) to the bottom center of the VS drop.
6. Load, seal and plunge HSV Device within 80 seconds, not to exceed 110 seconds after initial exposure to VS.
NOTE: Load after specimen is completely dehydrated and stable at the bottom of the drop.
7. Refer to HSV Device Loading Protocol diagram and product insert for detailed loading instructions.