Vector Database
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Vector database is a digital-only collection of vector backbone information compiled by Addgene from third party sources.
This vector is NOT available from Addgene and the database is no longer actively maintained.
This vector is not available from Addgene.
Plasmid: pRB395
Information
- Source/Vendor
- ATCC
- Plasmid Type
- Unspecified
- Cloning Method
- Unknown
- Size
- 6600
- Notes
- Deposited by: Reinhold Bruckner Neo confers resistance to neomycin and kanamycin and ble confers resistance to bleomycin and phleomycin. [1] Terminator-cloning shuttle vector using the expression of chloramphenicol acetyltransferase as the reporter. [1] The cat gene was derived from pUB112 by deletion of the promoter and the regulatory inverted repeat, resulting in constitutive cat gene expression under control of the vegII promoter. [1] The Bacillus subtilis promoter vegII initiates transcription in both B. subtilis and E. coli. [1] Structural stability of the plasmid in B. subtilis can be affected by high levels of protein production. Under these conditions, cell growth and stability may be improved by reducing the antibiotic concentration in the media. [1] May not be suitable for cloning very strong expression signals. [1] The order of the major features in the plasmid is: To terminator - vegII promoter - HindIII/MCS/EcoRI - cat - rrnB terminator - ampR - pMB1 ori - pUB110 ori - neoR - bleR. [1] Restriction digests of the clone give the following sizes (kb): EcoRI--6.8; BamHI--6.8; BglI/BglII--3.5, 3.3. (ATCC staff) Medium is 1227 LB plus ampicillin. Hosts: E.coli, E.coli HB101, Bacillus subtilis, B.subtilis DB403. (Information source: VectorDB ( http://seq.yeastgenome.org/vectordb ).)
- Catalog Number
- 77376
- Stable
- Unspecified
- Constitutive
- Unspecified
- Viral/Non-Viral
- Unspecified