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DNase

DNase I,无RNase

Company: Thermo Fisher Scientific
Catalog#: EN0523
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Molecular and Phenotypic Characterization Following RNAi Mediated Knockdown in Drosophila
Author:
Date:
2021-02-20
[Abstract]  

Loss of function studies shed significant light on the involvement of a gene or gene product in different cellular processes. Short hairpin RNA (shRNA) mediated RNA interference (RNAi) is a classical yet straightforward technique frequently used to knock down a gene for assessing its function. Similar perturbations in gene expression can be achieved by siRNA, microRNA, or CRISPR-Cas9 methods also. In Drosophila genetics, the UAS-GAL4 system is utilized to express RNAi and make ubiquitous and tissue-specific knockdowns possible. The UAS-GAL4 system borrows genetic components of S. cerevisiae, hence rule out the possibility of accidental expression of the system. In particular, this technique uses a target-specific shRNA, and the expression of the same is governed by the upstream activating

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[摘要]  [摘要]功能丧失的研究为基因或基因产物在不同细胞过程中的参与提供了重要启示。短发夹RNA(shRNA)介导的RNA干扰(RNAi)是一种经典而直接的技术,经常用于敲低基因以评估其功能。也可以通过siRNA,microRNA或CRISPR-Cas9方法实现类似的基因表达扰动。在果蝇遗传学中,UAS-GAL4系统用于表达RNAi,并使遍在和组织特异性的基因敲除成为可能。UAS-GAL4系统借鉴了酿酒酵母的遗传成分,因此排除了系统意外表达的可能性。特别地,该技术使用靶标特异性shRNA,并且其表达受上游激活序列(UAS)支配。由特定启动子调节的GAL4受控表达可以普遍或以组织特异性方式驱动干扰RNA的表达。通过RNA分离和半定量RT-PCR反应,然后进行琼脂糖凝胶电泳来测量敲低效率。我们还采用了免疫染色程序来评估击倒效率。

RNAi为研究人员提供了降低基因产物水平(相当于亚同型条件)并研究结果的选择。基于UAS-GAL4的RNAi方法提供了基因表达的时空调节,还有助于推断早期发育阶段所需的基因功能。


[背景]果蝇果蝇(果蝇)是在研究实验室经常使用的一种通用模式生物。果蝇易于处理,繁殖和维护。而且,精心制作却寿命短,繁殖力高的果蝇具有更多的优势。果蝇遗传学工具的易用性有助于发展对基因功能的全面了解。由于果蝇基因中有60%与人类基因同源,并且具有前面提到的其他优点,因此果蝇是研究体内基因功能的显而易见的模型生物。 ...

Detection and Visualization of Specific Gene Transcripts by in situ RT-PCR in Nematode-Infected Arabidopsis Root Tissue
Author:
Date:
2015-09-20
[Abstract]  This protocol describes an effective method of in situ RT-PCR that was developed to localize specific gene expression directly in thin cross-sections of nematode feeding sites induced by the cyst nematode Heterodera schachtii (H. schachtii) or the root-knot nematode Meloidogyne incognita (M. incognita) in Arabidopsis roots using DIG (Digoxigenin-11dUTP) labeling coupled with AP (alkaline phosphatase) and nitro-blue tetrazolium/5-bromo-4-chloro-3'-indolylphosphate-based detection. This method is applicable to any other Arabidopsis root tissue. [摘要]  该方案描述了原位 RT-PCR的有效方法,其被开发用于直接在由胞囊线虫Heterodera schachtii诱导的线虫摄食位点的薄横截面中定位特异性基因表达。 在拟南芥根中( H。schachtii )或根结线虫 Meloidogyne incognita 使用与AP(碱性磷酸酶)和硝基蓝四唑/5-溴-4-氯-3'-吲哚磷酸盐基检测偶联的DIG(地高辛-11dUTP)标记。 该方法适用于任何其他拟南芥根组织。

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