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Boric Acid

硼酸

公司名称: Sigma-Aldrich
产品编号: B0394
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Identification of Natural Hybrids by SSR Markers in Mussaenda
Author:
Date:
2016-07-05
[Abstract]  Detection of natural hybrids is of great significance for plant taxonomy, reproductive biology, and population genetic studies. Compared with methods depending on morphological characters, molecular markers provide reliable and much more accurate results. This protocol describes approaches employing microsatellite (SSR) markers to identify inter-specific hybrids in Mussaenda (Rubiaceae). [摘要]  自然杂交的检测对植物分类学,生殖生物学和群体遗传学研究具有重要意义。 与依赖于形态特征的方法相比,分子标记提供可靠和更准确的结果。 该协议描述了采用微卫星(SSR)标记来鉴定Mussaenda(茜草科)中的特异性杂交体的方法。

Primer Extension Analysis of HBV DNA with Strand-Specific Primers
Author:
Date:
2015-08-05
[Abstract]  We performed primer extension assay to determine which steps of HBV DNA synthesis (i.e., minus- and plus-strand DNA synthesis and circularization of RC DNA) are affected by phosphoacceptor site mutations in C protein. In these experiments, we used several specific oligonucleotide primers. For quantitation, the level of extended DNA (ED) was normalized to the level of a single internal standard (IS) DNA. [摘要]  我们进行引物延伸测定以确定HBV DNA合成的哪些步骤(即,负链和正链DNA合成和RC DNA的环化)受C蛋白中的磷酸受体位点突变的影响。 在这些实验中,我们使用几种特异性寡核苷酸引物。 为了定量,将延伸DNA(ED)的水平标准化为单个内标(IS)DNA的水平。

Biotinylation of Cell Surface Proteins
Author:
Date:
2012-05-05
[Abstract]  Membrane proteins are major sensors of extracellular stimuli and initiators of intracellular signal transduction, and their abundance on the cell surface in particular is often dynamically regulated even when there are no significant changes of their total abundance in a cell. This protocol is designed to biochemically label and separate membrane proteins on the plasma membrane from those in the intracellular compartments. In conjunction with co-immunoprecipitation and western blot analysis, functional analysis of dynamic interaction of membrane proteins with other membrane proteins or ... [摘要]  膜蛋白是细胞外的刺激和细胞内信号转导发起的主要传感器,他们大量并特定的存在细胞表面上。它们虽然受到动态调节,但是在细胞中的总量没有显著变化。该方法的目的是给浆膜的膜蛋白打上生化标签,并且在细胞内将它们分离出来。与免疫共沉淀和免疫印迹分析相结合,膜蛋白和其他膜蛋白或者细胞内接头和效应蛋白的动态交互功能分析,都可以实现。

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