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用于受精的单细胞小鼠卵的培养基制备。

Preparation of culture media for fertilized one-cell mouse eggs.

作者信息

Carter D A

机构信息

Neuropeptide Laboratory, Institute of Molecular and Cell Biology, National University of Singapore, Republic of Singapore.

出版信息

Methods Mol Biol. 1993;18:141-3. doi: 10.1385/0-89603-245-0:141.

Abstract

Two types of culture media are required for the in vitro manipulations involved in the process of making transgenic mice. (1) M16: This is used for maintenance of eggs in microdrop cultures in a 37°C incubator gassed with 5% CO₂. Since this medium is buffered with bicarbonate alone and the eggs are extremely susceptible to pH changes, it is not suitable for maintaining eggs outside the incubator. (2) M2: This is used for maintaining eggs outside the incubator during prolonged manipulations, such as collection or microinjection. M2 has essentially the same components as M16, although the bicarbonate is partially replaced with HEPES buffer to facilitate survival outside the CO₂ incubator. However, the eggs should not be maintained in M2 for periods longer than 30 mins.

摘要

制作转基因小鼠的过程中涉及的体外操作需要两种培养基。(1)M16:用于在37°C、含5% CO₂的培养箱中微滴培养时保存卵子。由于这种培养基仅用碳酸氢盐缓冲,而卵子对pH变化极为敏感,所以它不适合在培养箱外保存卵子。(2)M2:用于在长时间操作(如采集或显微注射)期间在培养箱外保存卵子。M2的成分与M16基本相同,不过碳酸氢盐部分被HEPES缓冲液取代,以便于在CO₂培养箱外存活。然而,卵子在M2中保存的时间不应超过30分钟。

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