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拟南芥下胚轴原生质体的简单培养方法。

A simple culture method for Brassica hypototyl protoplasts.

机构信息

Department of Crop Science, University of Guelph, Guelph, Ontario, Canada.

出版信息

Plant Cell Rep. 1985 Feb;4(1):4-6. doi: 10.1007/BF00285492.

Abstract

Hypocotyl protoplasts from oil rape, Brassica napus L. cv. Isuzu were cultured in the dark at 25°C in a modified Nitsch and Nitsch medium containing 13% sucrose, 5 g/l Ficoll, 0.5 mg/l BAP, 1 mg/l NAA and 0.5 mg/l 2-4 D. Protoplasts floated on the surface of the medium and developed into microcolonies 0.5 mm in diameter in 4-6 weeks. The microcolonies also remained on the surface of the medium. Transfer to MS medium supplemented with 200 mg/l casein hydrolysate, 5mg/l BAP, 0.5 mg/l NAA and solidified with 0.6% agarose induced shoot regeneration in 3-4 weeks.

摘要

甘蓝型油菜胚性愈伤组织原生质体在黑暗条件下于 25°C 培养,使用改良的 Nitsch 和 Nitsch 培养基,内含 13%蔗糖、5g/L 菲可、0.5mg/L BAP、1mg/L NAA 和 0.5mg/L 2,4-D。原生质体漂浮在培养基表面,4-6 周后形成直径为 0.5 毫米的小菌落。小菌落也留在培养基表面。转移到添加 200mg/L 水解酪蛋白、5mg/L BAP、0.5mg/L NAA 的 MS 培养基,并以 0.6%琼脂糖固化,3-4 周后诱导芽再生。

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