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通过实时定量PCR测定转基因拷贝数。

Determination of transgene copy number by real-time quantitative PCR.

作者信息

Shepherd Colin T, Moran Lauter Adrienne N, Scott M Paul

机构信息

AimsBio, Inc., USA.

出版信息

Methods Mol Biol. 2009;526:129-34. doi: 10.1007/978-1-59745-494-0_11.

Abstract

Efficient methods to characterize transgenic plants are important to quickly understand the state of the transformant. Determining transgene copy number is an important step in transformant characterization and can differentiate between complex and simple transformation events. This knowledge can be extremely useful when determining what future experiments and uses the transgenic lines can be utilized for. The method described here uses real-time quantitative PCR to determine the transgene copy number present in the genome of the transformant. Specifically, this method measures the relative transgene copy number by comparing it with an endogenous gene with a known copy number. This method is a quick alternative to the Southern blot, a method that is commonly used to determine gene copy number, and is effective when screening large numbers of transformants.

摘要

表征转基因植物的有效方法对于快速了解转化体状态非常重要。确定转基因拷贝数是转化体表征的重要一步,并且可以区分复杂和简单的转化事件。在确定转基因品系可用于哪些未来实验和用途时,这些信息可能会非常有用。这里描述的方法使用实时定量PCR来确定转化体基因组中存在的转基因拷贝数。具体而言,该方法通过将其与具有已知拷贝数的内源基因进行比较来测量相对转基因拷贝数。该方法是常用于确定基因拷贝数的Southern印迹法的一种快速替代方法,在筛选大量转化体时非常有效。

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