毕赤酵母
基因
分子生物学
生物
重组DNA
质粒
标准曲线
基因组DNA
实时聚合酶链反应
基因剂量
遗传学
生物化学
基因表达
作者
Lan Hai-ying,Na Li,Qiao Mei Shi,Le Kang,Hongchao Chen
出处
期刊:Int J Biologicals
日期:2018-04-10
卷期号:41 (2): 63-67
标识
DOI:10.3760/cma.j.issn.1673-4211.2018.02.003
摘要
Objective
To detect the copy number of plasmin inhibitor gene Textilinin-1 in Pichia pastoris by fluorescence quantitative PCR.
Methods
The standard curves of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and Textilinin-1 genes were generated with the plasmids containing GAPDH and Textilinin-1 genes, respectively, and the genomic DNA of Pichia pastoris transformants containing Textilinin-1 gene was analyzed by fluorescence quantitative PCR. The copy number of Textilinin-1 gene in each transformant was calculated according to the double standard curves.
Results
The reaction efficiencies of GAPDH and Textilinin-1 genes were 95.04% and 96.36%, respectively. The coefficients of determination for standard curves of two genes were both 0.999, and both curves showed good reproducibility. Of the 10 transformants tested, the copy number of Textilinin-1 gene was 2.
Conclusion
A fluorescence quantitative PCR method is successfully developed and it is useful for detecting the copy number of Textilinin-1 gene in recombinant Pichia pastoris.
Key words:
Fluorescence quantitative PCR; Pichia pastoris; Gene copy number
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