pBR322 (OG589) pBR322 Low Copy Cloning Vector

Product Code: OG589R1
Product Code: OG589C1
Product Code: OG589G1

Product Description

Standard pBR322 cloning plasmid. It contians both Ampicillin and Tetracycline resistance. Copy number is typically between 10-100 per cell.

Plasmid Information

Product Name: pBR322

Product Code: OG589

Size (bp): 4361 bp

Bacterial Antibiotic Selection:

Origin and Compatibility:

Bacterial Copy Number:


Plasmid Purpose:

This plasmid contains the BR322 (low copy number) origin of replication and provides approximately 20 plasmid copies per bacterial cell. Low copy number plasmids are useful for very large transgenes or for transgenes that can be toxic to bacterial cells.

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Transcription Termination:

This plasmid contains three alternative transcription terminators for mammalian bacterial and bacteriophage (T7) expression. This means that only the promoter needs to be changed to alter the expression system you are using. We sell multiple promoters that can be used in each of these systems. The presence of each terminator does not reduce expression in the alternative systems.

BR322 Information:

BR322 is a wild type plasmid isolated from E.coli. It contains a low copy origin that allows for plasmid maintenance at a frequency of approximately 10-100 plasmid copies per cell. Typically this number is closer to 30-40 copies per cell. Most common cloning plasmids contain a derivative of the origin of replication in this plasmid called pUC. The pUC origin was created by removing the Rep repressor protein that normally regulates plasmid copy number in E.coli and also making a single point mutation in the origin of replication itself. The point mutation is the most important difference between the origin of replication.

This plasmid can be used as a general purpose low copy cloning vector.

Intellectual Property Status

This product is part of our SnapFastâ„¢ plasmid range, for more information on the intellectual property status of this plasmid please click here. For more information on the terms of our licences please click here.