Last data update: 24 January 2024 16:39 CET
Plasmid name: pBS-hTIRAP (LMBP 6809)
| New search | Print data sheet |
| Price category: | Cat. 1 (cf. price list) |
| Status: | GeneCorner non-core plasmid |
| Depositor's sequence: | p6809.gb |
| Sequence analysis results Genecorner: |
- |
| Cloned DNA: |
Human toll-interleukin 1 receptor (TIR) domain containing adaptor protein (TIRAP, Mal) isoform 1 Escherichia coli lac Z gene (lacZ); α part |
| Promoter: | Phage T3 promoter Phage T7 gene 10 promoter (T7g10) Escherichia coli lac operon promoter |
| Ribosome binding site: |
- |
| Terminator: | - |
| Selection marker: | Ampicillin (amp) |
| Replicon: | Phage f1 origin Escherichia coli plasmid pMB1 origin |
| Host range: | Escherichia coli |
| Further information: | - |
| EMBL Accession number: | - |
| Latest sequence update: | 06/11/2010 |
| Authenticity test: | The plasmid still needs to be subjected to the authenticity test. |
| Class: | Recombinant plasmid |
| Type: | Plasmid |
| History of deposit: | This plasmid was deposited by Prof. Dr R. Beyaert(1) (2). It was constructed by Dr H. Braun(1) (2). (1) Department for Molecular Biomedical Research, VIB, Ghent, Belgium (2) Department of Biomedical Molecular Biology, Ghent University, Ghent, Belgium |
| Plasmid reference: | - |
| Restricted distribution: | - BCCM MTA |
| Distributed as: | H/P active culture or plasmid DNA |
| Host for distribution: | Escherichia coli K12 DH10B |
| Host reference: | Grant et al., Proc. Natl. Acad. Sci. U.S.A. 87 (1990), 4645-4649 [PMID: 2162051] |
| Related host reference: | Durfee et al., J. Bacteriol. 190 (2008), 2597-2606 [PMID: 18245285] [DOI: 10.1128/JB.01695-07] |
| Cultivation medium: | LB-Lennox + ampicillin (100 μg/ml) |
| Cultivation temperature: | 37°C |
| Biosafety level: | L1 |
| Cultivation remark: | - |
| Other culture collection numbers: | - |
Refer in your Materials and Methods: |
pBS-hTIRAP (LMBP 6809) is available at BCCM/GeneCorner. This plasmid was deposited by Prof. Dr R. Beyaert . |
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.