
The conditional expression of hairpin constructs in Drosophila melanogaster has emerged in recent years as a method of choice in functional genomic studies. To date, upstream activating site-driven RNA interference constructs have been inserted into the genome randomly using P-element-mediated transformation, which can result in false negatives due to variable expression. To avoid this problem, we have developed a transgenic RNA interference vector based on the phiC31 site-specific integration method.
Research Subject Categories::NATURAL SCIENCES::Chemistry::Biochemistry::Functional genomics, 570, Tools: Genetic Engineering, Genetic Vectors, 500, Gypsy Insulator, UAS-Luciferase, Notch RNAi, Drosophila melanogaster, Gene Targeting, Animals, Drosophila Proteins, RNA Interference, AttP sites, Biology, Biotechnology
Research Subject Categories::NATURAL SCIENCES::Chemistry::Biochemistry::Functional genomics, 570, Tools: Genetic Engineering, Genetic Vectors, 500, Gypsy Insulator, UAS-Luciferase, Notch RNAi, Drosophila melanogaster, Gene Targeting, Animals, Drosophila Proteins, RNA Interference, AttP sites, Biology, Biotechnology
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