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 信息
信息 
		| 启动子 | PH | 
| 复制子 | pBR322 | 
| 终止子 | polyhedrin 3 | 
| 质粒分类 | 昆虫细胞杆状病毒组成型表达质粒 | 
| 质粒大小 | 9032bp | 
| 原核抗性 | Amp | 
| 克隆菌株 | DH5α | 
| 培养条件 | 37℃ | 
| 表达宿主 | 昆虫细胞 | 
| 诱导方式 | 组成性表达,无需诱导 | 
| 5'测序引物 | Polyhedrin-F:AAATGATAACCATCTCGC | 
| 3'测序引物 | Polyhedrin-R:GTCCAAGTTTCCCTG | 
| 质粒宿主 | 昆虫细胞 | 
| 质粒用途 | 蛋白表达 | 
| 原核抗性 | 氨苄青霉素 | 
 简介
简介
		
					    pVL1392
and pVL1393 are 9.8 kb vectors designed for use as baculovirus transfer
vectors. These transfer vectors contain recombination sequences which are
homologous to sequences in the baculovirus genome.Upon cotransfection, these
sequences undergo homologous recombination resulting in a recombinant viral
genome packaged in infectious viral particles.
    These vectors are nonfusion vectors,
which provide the AcMNPV polyhedrin enhancer-promoter sequences to drive high
expression, and a multiple cloning site, conveniently constructed in opposite
orientations, for simple subcloning. Translation initiation sequences must be
provided by the inserted cDNA.
    • Multiple cloning site polylinker,
positioned in opposite orientations
    •  Recombination sequences for
insertion into the baculovirus genome
    • Polyhedrin enhancer-promoter sequences for
high expression of recombinant protein Features for growth and maintenance in
E. coli:
    • Ampicillin gene for selection
    • pMB1 origin of replication from
pUC19 for high copy number growth
				


 
 
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