Claim · model-written summary
Three hours of PVS2 dehydration yielded 64% survival of encapsulated, vitrified and cryopreserved olive embryos.
Olea europaeaNot reportedMaterialGeneCompoundOrgan / stageInteractorInteractor roleSecond interactorSecond interactor roleComparatorSettingQualifier
Organisms pictured · Representative pictures of the matched species, not figures from the paper.
Verbatim
e0“Dehydration of beads for 3 h in PVS2 ensured higher survival (64%) of encapsulated-vitrified and cryopreserved (EVN) somatic embryos.”
t0“olive”
Title
R A Shibli; K H Al-Juboory PubMed
Other claims from this paper (7)
- Observation Olive somatic embryos were successfully cryopreserved by encapsulation-dehydration.
- Observation Olive somatic embryos were successfully cryopreserved by encapsulation-vitrification.
- Intervention effect Encapsulation-dehydration produced a maximum olive embryo survival of 48% at 21.1% bead moisture after four hours.
- Intervention effect Preculture in 0.75 M sucrose for four days produced 40% olive embryo regrowth after cryopreservation.
- Intervention effect One day of thermal treatment at 30 degrees C raised survival of encapsulated-dehydrated olive embryos to 58%.
- Intervention effect One day of thermal treatment at 30 degrees C raised survival of encapsulated-vitrified olive embryos to 68%.
- Observation Plantlets from cryopreserved and control olive embryos were phenotypically similar.