FVB/NIco-Tg(Pcp2/Jun)18Dcrl/Cnrm
| Status | Available to order |
| EMMA ID | EM:00120 |
| Citation information | RRID:IMSR_EM:00120 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
| International strain name | FVB/NIco-Tg(Pcp2/Jun)18Dcrl/Cnrm |
| Alternative name | L7-c-jun-Tg |
| Strain type | Transgenic Strains |
| Allele/Transgene symbol | Tg(Pcp2/Jun)18Dcrl |
| Gene/Transgene symbol | Tg(Pcp2/Jun)18Dcrl |
Information from provider
| Provider | Daniela Carulli |
| Provider affiliation | DIP. DI NEUROSCIENZE, Univ. di Torino |
| Phenotypic information | To generate the L7-c-Jun hybrid transgene the c-Jun cDNA was inserted into a vector named L7deltaAUG. This vector includes 1 kb of the Pcp2 (or L7) gene promoter, the L7 4 exons and 3 introns, and 200 bp downstream the TGA stop codon of the L7 gene, from which the normal and all potential ATGs were removed. The c-Jun cDNA was inserted into the unique BamHI site in the 4th exon of the L7 gene. No major defect so far detected. |
| References |
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Information from EMMA
| Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Literature references
- Regenerative and survival capabilities of Purkinje cells overexpressing c-Jun.;Carulli Daniela, Buffo Annalisa, Botta Cristina, Altruda Fiorella, Strata Piergiorgio, ;2002;The European journal of neuroscience;16;105-18; 12153535