pCAMBIA1391植物表达质粒   货号:P0625
	
	
		
	来源:
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	作者:shhebio
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	发布时间: 2018-04-24
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	193 次浏览
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			 信息
信息 
		
	 
	
		
			
				
					
						| 启动子 | 无 | 
					
						| 复制子 | pVS1 oriV,pUC ori | 
					
						| 终止子 | NOS terminator | 
					
						| 质粒大小 | 10658bp | 
					
						| 原核抗性 | Kan | 
					
						| 真核抗性 | Hyg | 
					
						| 克隆菌株 | Stbl3 | 
					
						| 培养条件 | 37℃ | 
					
						| 质粒宿主 | 植物 | 
					
						| 质粒用途 | 蛋白表达 | 
					
						| 原核抗性 | 卡那霉素 | 
					
						| 真核抗性 | 潮霉素 | 
				
			
			
			
		 
	 
 
	
		
			 简介
简介 
		
	 
	
		
			
				        pCAMBIA1391是一个植物启动子检测报告载体,可通过MCS克隆进需要研究的启动子。    
			
			
				       The pCambia vector backbone is derived from the pPZP vectors. The pCambia1391 vector offers:
              High copy number in E.coli for high DNA yields  pVS1 replicon for high stability in Agrobacterium
              Small size  Restriction sites designed for modular plasmid modifications and small but adequate poly-linkers for introducing your DNA of interest 
              Bacterial selection with kanamycin 
              Plant selection with hygromycin B 
              Simple means to construct translational fusions to gusA reporter genes 
       Plant selection genes in the pCambia vectors are driven by a double-enhancer version of the CaMV35S promoter and terminated by the CaMV35S polyA signal. Reporter genes feature a hexa-Histidine tag at the C-terminus to enable simple purification on immobilized metal affinity chromatography resins. Designed to utilize gusA as a true reporter of gene expression by fusion construction this vector contains a promoterless, non-intron gusA gene that retains the initiation codon of the NcoI site. This permits simple construction of carboxy-terminus protein fusions to gusA.
				
				 
			
		 
	 
 
	
		
			 图谱
图谱