摘要
【目的】 获得SPA Ⅰ基因克隆及亚克隆,并进行序列分析,为研究SPA 基因结构、表达调控、基因工程生产奠定基础。【方法】 以正常人血白细胞染色体DNA 为模板,采用PCR 及基因克隆技术,获得pBS/SPA Ⅰ克隆和pUC19/630bp 亚克隆,测序证实之。【结果】 测序结果显示,与已发表的SPA Ⅰ序列相比,未发现基因突变。【结论】 证实获得的基因为SPA Ⅰ。
Objective To get clone and subclone of Chinese pulmonary surfactent protein A and sequence it,which will be the base of the further study in SP A gene structure,expression control and genetic engineering. Methods pBS/SP A Ⅰ and pUC19/630bp clone was got from the normol Chinese chromosome DNA in WBC by PCR and gene cloning,and proven with measuring the sequence. Results Compared with SP A Ⅰ sequence that was published,there is no mutation. Conclusion :SP A clone was got.
出处
《中国儿童保健杂志》
CAS
2000年第1期37-39,共3页
Chinese Journal of Child Health Care
基金
广东省自然科学基金!项目
序号950558
关键词
克隆
亚克隆
SP-A
肺
Pulmonarg surfent Proteina, Clone, Sub clone.