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Permits
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These permits may be required for shipping this product:
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Customers located in the state of Hawaii will need to contact the Hawaii Department of Agriculture to determine if an Import Permit is required. A copy of the permit or documentation that a permit is not required must be sent to ATCC in advance of shipment.
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Vector Information
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Size (kb): 5.8000001907348630 Vector: pEX11 (plasmid) Promoters: Promoter lambda PR Construction: pEX1, oligonucleotide Marker(s):ampR Construct size (kb): 5.800000190734863 Features: marker(s): ampR
promoter: lambda PR
replicon: pMB1
terminator: phage fd
enhancer: none
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Applications
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expression vector vector for constructing cDNA libraries
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Comments
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Restriction digests of the clone give the following sizes (kb): EcoRI--5.8; BamHI--5.8; PstI--5.8; EcoRI/EcoRV--4.3, 1.9; SalI--5.8. This strain is resistant to 100 ug/ml ampicillin. The recombinant fusion protein generated using this vector is not solubilized in Triton X-100 lysis procedures and is thus easily purified, resistant to proteolysis, and easily detected by direct immunoscreening. This is one of three bacterial expression vectors (pEX11, ATCC 37708; pEX12, ATCC 37709; and pEX13, ATCC 37710) which differ by translational reading frames and which express cro-lacZ fusion proteins regulated by the PR promoter of bacteriophage lambda. This was constructed from pEX1 by the ligating a synthetic oligonucleotide into pEX1 cut with XmaI and BamHI. The oligonucleotide added several unique restriction sites.
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References
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Kusters JG, et al. Improvement of the cloning linker of the bacterial expression vector pEX. Nucleic Acids Res. 17: 8007, 1989. PubMed: 2678010
Stanley KK, Luzio JP. Construction of a new family of high efficiency bacterial expression vectors: identification of cDNA clones coding for human liver proteins. EMBO J. 3: 1429-1434, 1984. PubMed: 6086324
Bernard A Van Der Zeijst, personal communication
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