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PURPOSE: To establish the mutant Myocilin gene plasmid in order to study the function of Myocilin. METHODS: The mutant site was induced by site-directed mutagenesis. This plasmid were transfected into human trabecular meshwork cells (HTM cells) by cationic liposomes and the expression of Myocilin was examined by RT-PCR and Western blot analysis. RESULTS: The mutant plasmid were correctly constructed. Myocilin was efficiently expressed in HTM cells transfected with this plasmid. CONCLUSION: The constructed eukaryote expression plasmid pcDNA-MYOC-P370L could express Myocilin in HTM cells in vitro. LA: Chinese
Dr. L. Wang, Key Laboratory of Ophthalmology of Ministry of Education and Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou 510060, China
2.5.1 Trabecular meshwork (Part of: 2 Anatomical structures in glaucoma > 2.5 Meshwork)
3.4.2 Gene studies (Part of: 3 Laboratory methods > 3.4 Molecular genetics)