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- W78862461 abstract "Transgenic cotton has widely been employed both in commercial cultivation and basic research. It is essential to determine which plants contain the transgene and in how many copies after transgenic cotton plants are generated. A TaqMan quantitative real-time polymerase chain reaction (Tq RT-PCR) method is described here to examine transgene copy number in transgenic cotton plants. The estimation of two transgene elements, the target gene of green fluorescence protein (GFP) and the selective gene of neomycin phosphotransferase II (NPTII), is used as an example to detail each step in Tq RT-PCR procedure, including endogenous reference gene selection, reference plasmid construction, primer-probe design, DNA extraction, real-time PCR, and data analysis. Comparing with traditional approach-Southern hybridization analysis, this method can be used efficiently in screening large number of T0 transgenic cotton plants at early stage of transformation process as well as identifying transgene homozygotes in a segregation population." @default.
- W78862461 created "2016-06-24" @default.
- W78862461 creator A5056243974 @default.
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- W78862461 date "2012-10-16" @default.
- W78862461 modified "2023-10-05" @default.
- W78862461 title "Estimating the Copy Number of Transgenes in Transformed Cotton by Real-Time Quantitative PCR" @default.
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- W78862461 doi "https://doi.org/10.1007/978-1-62703-212-4_9" @default.
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