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요약정보
人隔蛋白7的真核表达载体的构建及表达 / Construction and Expression of SEPT7 Expression Vector
Resource Type
Academic Journal
Authors
贾志凡
;
浦佩玉
;
康春生
;
王广秀
;
张志勇
;
裘明哲
;
黄强
;
JIA Zhifan
;
PU Peiyu
;
KANG Chunsheng
;
WANG Guangxiu
;
ZHANG Zhiyong
;
QIU Mingzhe
;
HUANG Qiang
Source
医学分子生物学杂志 / JOURNAL OF MEDICAL MOLECULAR BIOLOGY
. 4(5):401-405
Subject
人隔蛋白7
质粒构建
胶质瘤细胞
细胞周期
Language
Chinese
ISSN
1672-8009
Online Access
Find it @ DONGA
초록
目的 构建人隔蛋白7(SEPT7,hCDC10/SEPT7)的表达载体并对U251人脑恶性胶质瘤细胞系进行转染且检测其表达.方法 RT-PCR方法扩增SEPT7 cDNA片段,并将扩增的片段插入pCDNA3真核表达载体,构建成含SEPT7 cDNA的重组载体pCDNA3/SEPT7,以脂质体介导该质粒转染人脑恶性胶质瘤细胞系U251,应用RT-PCR和免疫荧光染色鉴定转染细胞中hCDC10/SEPT7的表达.用流式细胞术对转染前后的U251细胞进行细胞周期分析.结果 成功构建含SEPT7 cDNA的重组载体pCDNA3/SEPT7,并使其稳定转染U251细胞,在转染的细胞中,证实有SEPT7 mRNA表达上调.细胞周期检测结果G0/G1期细胞增多,SPF降低.结论 成功构建SEPT7表达载体,并在人脑恶性胶质瘤细胞系获得表达,延迟细胞周期进展.
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