1) thin-cross-section culture
薄片培养
1.
The high efficiency of shoot differentiation was obtained from the thin-cross-section cultured at 24 ℃ in light for 5 days after being cultured at 30 ℃ in darkness for 15 days.
采用横切薄片培养方法建立了香蕉基因转化的适宜受体系统。
2) Thin cell layer
薄层培养
5) scale culture
鳞片培养
6) slice culture
切片培养
1.
In this paper the detailed procedures for slice culture technique of brain tissue were introduced, including the equipments required, reagents, preparation of brain tissue slice and incubation.
本文对脑组织切片培养技术进行了详细的介绍，包括仪器设备、培养液的配制、脑组织切片制备及培养过程等。
