A method for
cryopreservation and
recovery of
larch olgensis embryogenic
callus relates to the
biotechnology field of forest breeding, and comprises the following steps: selecting an embryogenic
cell line induced by immature seeds of
larch olgensis, and subculturing the embryogenic
cell line for 3-5 days to obtain embryogenic
callus as a standby material; carrying out gradient pre-culture at the
molar concentrations of 0.2 mol / L and 0.4 mol / L in sequence, wherein the culture is carried out at each concentration for 20-48 hours; after pre-culture, putting the embryogenic
callus into a freezing tube, and adding a sterile freezing protection solution; and putting the freezing
pipe into a programmed cooling box for programmed cooling, and immediately putting the freezing
pipe into a
liquid nitrogen biological container for storage. The method disclosed by the invention is simple and convenient in operation steps and obvious in effect, the subculture
age limit of the larix olgensis embryonic callus is slowed down, and relatively good
cell viability and development potential in the initial stage of induction are maintained, so that the occurrence of variation is effectively reduced, manpower and
material resources consumed by long-term subculture materials can be saved, and the production cost is reduced. The method is of great significance to theoretical and practical application research of larix olgensis.