Last data update: 04 July 2022 09:25 CEST
Plasmid name: pET-28a-MBP-TEV-Gadc1 (LMBP 11987)
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|Price category:||Cat. 3 (cf. price list)|
|Status:||GeneCorner core plasmid|
(View with Genome Compiler)
Gadus morhua callarias parvalbumin beta cDNA (Gad c 1, Gad c1)|
Escherichia coli maltose ABC transporter periplasmic binding protein cDNA (malE, GeneID 948538); mature sequence, N-terminal
Thrombin recognition site; N-terminal
Tobacco etch virus (TEV) protease recognition site; N-terminal
Histidine tag (His-tag); N-terminal
Escherichia coli DNA-binding transcriptional repressor LacI cDNA (lacI, GeneID 945007)
Histidine tag (His-tag); C-terminal
|Promoter:||Phage T7 gene 10 promoter (T7g10) with lac operator (T7lac)
Escherichia coli lac repressor promoter (lacI)
|Ribosome binding site (RBS) of the phage T7 gene 10 (T7g10)|
|Terminator:||Phage T7 gene 10 terminator (T7g10)|
|Selection marker:||Neomycin (neo; kanamycin (kan))|
|Replicon:||Escherichia coli plasmid pMB1 origin
Phage f1 origin
|Host range:||Escherichia coli|
|Further information:||The plasmid was constructed by cloning the G. morhua callarias (Baltic cod) Gad c 1 coding sequence, optimised for E. coli, into the BamHI/XhoI opened pET28a-MBP-TEV vector.
The plasmid was designed to express the malE-Gad c 1 fusion protein in E. coli BL21(DE3). The plasmid encodes for the mature form of the E. coli maltose binding protein, which does not contain a signal sequence, hence the protein will remain in the cytosol.
The N-terminal His-tag can be removed via a thrombin recognition site, while the maltose binding protein can be separated from the G. morhua callarias Gad c 1 allergen via the TEV protease recognition site. The His-tag at the C-terminal end of the allergen is not functional in this plasmid.
The amino acid sequence of the G. morhua callarias Gad c 1 allergen corresponds with GenBank accession number P02622.1.
|EMBL Accession number:||P02622.1, view at EMBL, GenBank, DDBJ|
|Latest sequence update:||06/11/2019|
|Authenticity test:||This plasmid has been fully sequenced.|
|History of deposit:||The plasmid was deposited by Dr G. Zvirblis(1). It was constructed by A. Imbrasaitė(1) and Dr G. Zvirblis(1).
(1) Institute of Biotechnology, Vilnius University, Vilnius, Lithuania
|Restricted distribution:||- BCCM MTA|
|Distributed as:||H/P active culture or plasmid DNA|
|Host for distribution:||Escherichia coli K12 DH5αT1R|
|Related host reference:||Killmann et al., J. Bacteriol. 178 (1996), 6913-6920 [PMID: 8955314] [DOI: 10.1128/jb.178.23.6913-6920.1996]
|Cultivation medium:||LB-Lennox + kanamycin (50 μg/ml)|
|Other culture collection numbers:||-|
Refer in your Materials and Methods:
|pET-28a-MBP-TEV-Gadc1 (LMBP 11987) is available at BCCM/GeneCorner. The plasmid was deposited by Dr G. Zvirblis.|
Note: Up-to-date, validated data are enclosed with the biological material. Nevertheless, these data are a snapshot at a given moment; further updates are always possible.