Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Size (kb): 4.5500001907348630
Vector: pGCAT-C (plasmid)
Promoters: Promoter T7
Construction: pSB1, pGEM4
Construct size (kb): 4.550000190734863
Features: insert detection: CAT
promoter: SP6, T7
vector permitting RNA synthesis in vitro
Restriction digests of the clone give the following sizes (kb): PvuII--3.0, 1.5; HincII--3.0, 1.5; EcoRI--4.25, 0.3.
A plasmid shuttle vector for investigating promoter and/or enhancer elements. Has a polylinker upstream of reporter CAT gene, SP6 and T7 promoters for in vitro RNA synthesis and low basal CAT expression in eukaryotic cells.
The sequence at the junction of the multiple cloning site and CAT is GAATTCGAGC and at the junction of SV40 and SP6 is GGATCAGCTT.
The polylinker is in opposite orientation in pGCAT-A (ATCC 37640)
and pGCAT-C (ATCC 37641)
BamHI/HindIII fragment of pSB1 (CAT) was cloned into the HindIII site of pGEM-4. 2 hrs after ligation began the remaining BamHI and HindIII sites were filled in. Contains SV40 polyadenylation site and donor and acceptor sites of SV40 small-t intron.
Frebourg T, Brison O. Plasmid vectors with multiple cloning sites and cat-reporter gene for promoter cloning and analysis in animal cells. Gene 65: 315-318, 1988. PubMed: 2842234
Thierry Frebourg, personal communication