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改良的电穿孔缓冲液提高了花生原生质体的瞬时基因表达。

Improved electroporation buffer enhances transient gene expression in Arachis hypogaea protoplasts.

出版信息

Genome. 1995 Oct;38(5):858-63. doi: 10.1139/g95-113.

Abstract

An electroporation medium containing 50 mM glycine or 10 mM glycylglycine (glygly), 70 mM potassium glutamate, and 0.4 M mannitol was evaluated for its ability to improve transient β-glucuronidase (GUS) expression in immature cotyledonary protoplasts of Arachis hypogaea L. GUS activity in electroporated protoplasts was 8- to 430-fold greater than that obtained using any of other four commonly employed poration media. Analysis of viability and histochemical staining of protoplasts indicated that electroporation using the glycine- or glygly-based poration medium resulted in increased protoplast viability and GUS expression when compared with other poration media. Replacement of glygly with MES or HEPES buffers significantly reduced the level of GUS expression in electroporated protoplasts.

摘要

含有 50mM 甘氨酸或 10mM 甘氨酰甘氨酸(glygly)、70mM 谷氨酸钾和 0.4M 甘露醇的电穿孔缓冲液,用于评价其提高花生不成熟子叶原生质体瞬时β-葡萄糖醛酸酶(GUS)表达的能力。电穿孔原生质体中的 GUS 活性比使用其他四种常用的穿孔介质获得的活性高 8 至 430 倍。对原生质体活力和组织化学染色的分析表明,与其他穿孔介质相比,使用甘氨酸或 glygly 基穿孔缓冲液进行电穿孔可提高原生质体活力和 GUS 表达。用 MES 或 HEPES 缓冲液替代 glygly 显著降低了电穿孔原生质体中 GUS 表达的水平。

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