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Updated: Jul 9, 2026

In Situ Hybridization for the Precise Localization of Transcripts in Plants
Published on: November 23, 2011
[Application of enzyme-labeled probe in testing of transgenic plant]
Zhi-Ming Tu1, Lin Chen, Guang-Xiao Yang
1Key Laboratory of Molecular Biophysics of the Ministry of Education, China-UK Joint Lab, College of life Science & Technology, Huazhong University of Science & Technology Wuhan, 430074, China.
Abstract:
Used alkaline-phosphatase-labeled DNA as a probe to examine the expression of foreign UidA gene in transgenic plants. Alkaline phosphatase coupled with polyethyleneimine (PEI) using P-benzoquine as the cross-linking reagent was covalently linked to single-stranded DNA via glutraldehyde. Such DNA-enzyme complexes were used as a probe for dot hybridization and Southern blot. After hybridization and incubation with a substrate solution, results can be observed directly in three to six hours and the results showed that it was a sensitive, specific, rapid, safe and economical probe. Dot hybridization analysis showed that the UidA gene was transformed into the target plants and southern blot showed that there were at least 5 copies of UidA gene in transgenic plants.
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