■ 基本信息
别名: | Plasmid #16405 |
启动子: | CMV |
复制子: | pUC |
终止子: | SV40 poly(A) signal |
质粒大小: | 9237bp |
原核抗性: | Kan |
真核抗性: | EGFP |
克隆菌株: | Stbl3 |
培养条件: | 37度 |
诱导方式: | 无须诱导,瞬时表达 |
■ 质粒属性
质粒宿主: | 哺乳细胞,腺病毒 |
质粒用途: | 蛋白表达 |
片段类型: |
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片段物种: |
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原核抗性: | Kan |
真核抗性: |
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荧光标记: | 绿色
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■ 质粒简介
PAdTrack-CMV transgenic adenovirus vector to cell expression vector with CMV promoter and EGFP gene expression of green fluorescent protein tracking results, and use common pAdeasy1 vector maximum can be inserted into the 5.9kb, the use of common pAdeasy2 carrier can insert the 8.6kb. The specific use of the method can refer to the pAdeasy carrier system.
Recombinant adenoviruses provide a versatile system for gene expression studies and therapeutic applications. We here report a strategy which simplifies the generation and production of such viruses. A recombinant adenoviral plasmid is generated with a minimum of enzymatic manipulations, employing homologous recombination in bacteria rather than in eucaryotic cells. Following transfections of such plasmids into a mammalian packaging cell line, viral production is conveniently followed with the aid of green fluorescent protein, encoded by a gene incorporated into the viral backbone. Homogeneous viruses can be obtained from this procedure without plaque purification.This system should expedite the process of generating and testing recombinant adenoviruses for a variety of purposes.
pAdTrack-CMVprotocol.pdf(点击下载)
■ 质粒图谱
■ 质粒序列
质粒序列请下载:ZK722pAdTrack-CMV腺病毒质粒.txt