Please use this identifier to cite or link to this item: http://elib.usma.ru/handle/usma/1449
Title: Construction and validation of prestin overexpression adeno – associated virus vector in outer hair cells
Authors: Lin, Sh.
Wang, J.
Issue Date: 2019
Publisher: Федеральное государственное бюджетное образовательное учреждение высшего образования «Уральский государственный медицинский университет» Министерства здравоохранения Российской Федерации
Citation: Lin Sh., Wang J. Construction and validation of prestin overexpression adeno – associated virus vector in outer hair cells. Current issues of modern medicine and healthcare : collection of articles of the IV International (74 All-Russian) scientific-practical conference, 2019, no. 1, pp. 514-518.
Abstract: OBJECTIVE: By constructing cochlear hair cell recombinant Prestin adeno-associated virus-2 (AAV-2) vector, it provides a tool for the study of cochlear Prestin protein regulation. METHODS: The guinea pig Prestin gene was used as a template for PCR amplification and extraction. The AAV-2-Prestin vector was constructed by genetic engineering. The expression level of Prestin was detected by Western blot on the 1st, 3rd and 5th day after transfection of cultured cochlear hair cells. RESULTS: After transfecting HEK-293T cells with pAAV-EGFP-Prestin proviral plasmid, the expression of weak green fluorescent protein was observed on the 1st day, and the expression of green fluorescent protein was peaked on the 3rd day. Conclusion: The recombinant adeno-associated virus-2-Prestin vector was successfully constructed and has good transfection efficiency and persistence.
Keywords: OUTER HAIR CELLS
ADENO-ASSOCIATED VIRUS
PRESTIN
URI: http://elib.usma.ru/handle/usma/1449
Origin: Сборник статей "IV Международная (74 Всероссийская) научно-практическая конференция "Актуальные вопросы современной медицинской науки и здравоохранения". 2019. №1
Appears in Collections:Конференции, семинары, сборники

Files in This Item:
File Description SizeFormat 
USMU_Sbornik_statei_2019_1_120.pdf281,72 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.