Construction of eukaryotic expression vector encoding ATP synthase lipid-binding protein-like protein gene of Sj and its expression in HeLa cells
|Updated:2026-03-12
|
Construction of eukaryotic expression vector encoding ATP synthase lipid-binding protein-like protein gene of Sj and its expression in HeLa cells
Construction of eukaryotic expression vector encoding ATP synthase lipid-binding protein-like protein gene of Sj and its expression in HeLa cells
解放军医学杂志(英文版)2008年第2期 页码:94-97
Affiliations:
Author bio:
Funds:
the Scientific Research Foundation of Education Committee of Hunan (07C713 and 07C708)
DOI:
中图分类号:Q78
纸质出版:2008
Accepted:
Scan QR Code
Construction of eukaryotic expression vector encoding ATP synthase lipid-binding protein-like protein gene of Sj and its expression in HeLa cells[J]. 解放军医学杂志(英文版), 2008,(2):94-97.
[1].Construction of eukaryotic expression vector encoding ATP synthase lipid-binding protein-like protein gene of Sj and its expression in HeLa cells[J].Journal of Medical Colleges of PLA,2008(02):94-97.
Construction of eukaryotic expression vector encoding ATP synthase lipid-binding protein-like protein gene of Sj and its expression in HeLa cells[J]. 解放军医学杂志(英文版), 2008,(2):94-97.DOI:
[1].Construction of eukaryotic expression vector encoding ATP synthase lipid-binding protein-like protein gene of Sj and its expression in HeLa cells[J].Journal of Medical Colleges of PLA,2008(02):94-97.DOI:
Construction of eukaryotic expression vector encoding ATP synthase lipid-binding protein-like protein gene of Sj and its expression in HeLa cells
摘要
Abstract
<
正
>
Objective:To clone and construct the recombinant plasmid containing ATP synthase lipid-binding protein-like protein gene of Schistosoma japonicum
(SjAslp) and transfer it into mammalian cells to express the objective protein. Methods:By polymerase chain reaction (PCR) technique
SjAslp was amplified from the constructed recombinant plasmid pBCSK
+
/SjAslp
and inserted into cloning vector pUCm-T.Then
SjAslp was subcloned into an eukaryotic expression vector pcDNA3.1(+).After identifying it by PCR
restrictive enzymes digestion and DNA sequencing
the recombinant plasmid was transfected into HeLa cells using electroporation
and the expression of the recombinant protein was analyzed by immunocytochemical assay.Results:The specific gene fragment of 558 bp was successfully amplified.The DNA vaccine of SjAslp was successfully constructed.Immunocytochemical assay showed that SjAslp was expressed in the cytoplasm of HeLa cells.Conclusion:SjAslp gene can be expressed in eukaryotic system
which lays the foundation for development of the SjAslp DNA vaccine against schitosomiasis.
关键词
Keywords
references
The trial reading is over, you can activate your VIP account to continue reading.