Murine brain tissues with human cytomegalovirus infection: a proteomic study
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Murine brain tissues with human cytomegalovirus infection: a proteomic study
Murine brain tissues with human cytomegalovirus infection: a proteomic study
解放军医学杂志(英文版)2010年25卷第2期 页码:65-74
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Author bio:
Funds:
Supported by the Program of Science and Technology from Shenzhen City, Guangdong Province (200802051)
DOI:
中图分类号:R742.9
纸质出版:2010
Accepted:
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Murine brain tissues with human cytomegalovirus infection: a proteomic study[J]. 解放军医学杂志(英文版), 2010,25(2):65-74.
[1].Murine brain tissues with human cytomegalovirus infection: a proteomic study[J].Journal of Medical Colleges of PLA,2010,25(02):65-74.
Murine brain tissues with human cytomegalovirus infection: a proteomic study[J]. 解放军医学杂志(英文版), 2010,25(2):65-74.DOI:
[1].Murine brain tissues with human cytomegalovirus infection: a proteomic study[J].Journal of Medical Colleges of PLA,2010,25(02):65-74.DOI:
Murine brain tissues with human cytomegalovirus infection: a proteomic study
摘要
Abstract
Objective: To establish two-dimensional electrophoresis profiles with high resolution and reproducibility from murine brain tissues by human cytomegalovirus(HCMV) infection and paired murine brain tissues and to identify the differential expression proteins. Methods: Forty Kunming mice were randomly divided into infection group (20) injected with HCMVAD169 and control group (20) injected with saline into their brain. After 30 days
the murine brain tissues by HCMV infection and paired murine brain tissues were separated by two-dimensional gel electrophoresis(2-DE)
analyzed by Image Master 2D software
and identified by peptide mass fingerprint(PMF) and database searching
and make Western blotting analyses the differential expression of individual proteins. Results: Well resolved
reproducible 2-D maps of the above tissues were obtained.Some of the different proteins identified by mass spectrometry(MS) were matched in the SWISS-2D PAGE database
Western blotting analyses were further carried out to verify the differential expression of individual proteins. Conclusion: These data will be valuable for studying the diagnosis of disease at an early stage
mechanisms of pathogenic and the key to the development of anti-HCMV medicine.
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