格斯报告系统
报告基因
葡萄糖醛酸酶
β-葡萄糖醛酸酶
生物搬运器
拟南芥
基因
生物
发起人
内生
克隆(编程)
分子生物学
基因表达
细胞生物学
遗传学
生物化学
突变体
程序设计语言
计算机科学
作者
Zhe Liang,Hilde-Gunn Opsahl-Sorteberg
出处
期刊:Methods in molecular biology
日期:2019-01-01
卷期号:: 103-108
被引量:1
标识
DOI:10.1007/978-1-4939-8988-1_9
摘要
The DEFECTIVE KERNEL1 (DEK1) gene encodes the unique plant calpain protein, which is fundamental for cell specification, development, and growth of land plants. The β-glucuronidase (GUS) reporter gene system has been used to characterize and localize gene expression over several decades. When cloning a promoter upstream of the uidA/GUS reporter gene, you visualize when the promoter is activating expression by monitoring enzymatic activity of GUS, by detecting β-glucuronidase cleavage products. Here we describe a protocol for monitoring the DEK1 promoter activity in different tissues in Arabidopsis by GUS staining.
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