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Browse > Connie Cepko > Matsuda et al > pCAG-Cre:GFP
Plasmid 13776: pCAG-Cre:GFP
Gene/insert name: Cre-GFP fusion protein
Alternative names: Cre recombinase
Insert size (bp): 1784
Species of gene(s): Bacteriophage P1
Fusion proteins or tags: GFP
Terminal: C terminal on insert
Vector backbone: pCAGEN  (Search Vector Database)
Type of vector: Mammalian expression
Backbone size (bp): 4779
Cloning site 5': EcoRI
Site destroyed during cloning: No
Cloning site 3': NotI
Site destroyed during cloning: No
5' Sequencing primer: pCAG-F  (List of Sequencing Primers)
Bacteria resistance: Ampicillin
High or low copy: High Copy
Grow in standard E. coli @ 37C: Yes
If you did not originally clone this gene, from whom and where did you receive the plasmid used to derive this plasmid: The coding sequence of Cre was amplified by PCR using pxCANCre (Kanegae et al. NAR 23, 3816-3821 (1995)) obtained from Dr. Saito I (Univ. of Tokyo) as a template. GFP was from pEGFP-N1 (Clontech).
Sequence:View sequence
Author's Map:View map
Plasmid Provided In:DH5a
Principal Investigator:Connie Cepko
Terms and Licenses:MTA

Comments: Kozak consensus sequence was added before the start ATG. GFP-tag was added at the C-terminus of Cre. Cre-GFP fusion protein is localized in the cell nucleus.

Addgene has sequenced a portion of this plasmid for verification. Click here for the sequencing result.

Click on map to enlarge

Selected features
CAG_enhancer 84 - 371
Orf frame 1 1533 - 802
pCAG_F_primer 1678 - 1697
CRE_NLS 1749 - 2744
Orf frame 3 1737 - 3500
EGFP_N_primer 2847 - 2826
EGFP 2781 - 3497
Orf frame 3 3638 - 2649
EGFP_C_primer 3434 - 3455
rb_glob_PA_terminator 3519 - 4020
M13_reverse_primer 4080 - 4062
M13_pUC_rev_primer 4101 - 4079
lac_promoter 4144 - 4115
SV40_origin 4285 - 4362
SV40_promoter 4250 - 4429
SV40pro_F_primer 4347 - 4366
SV40_PA_terminator 4443 - 4574
EBV_rev_primer 4531 - 4550
pBR322_origin 5417 - 4798
Orf frame 1 6432 - 5572
Ampicillin 6432 - 5572
AmpR_promoter 6502 - 6474
Unique restriction sites

SalI 1
SpeI 18
ApaI 863
SacII 1030
XbaI 1623
EcoRI 1719
NruI 1951
BstBI 2146
EcoRV 2288
ClaI 2543
NotI 3503
BglII 3584
PstI 4043
HindIII 4048
StuI 4418
FspI 5867

Article: Controlled expression of transgenes introduced by in vivo electroporation. Matsuda T et al. (Proc Natl Acad Sci U S A. 2007 Jan 5. ():. Pubmed)

Please acknowledge the principal investigator and cite this article if you use this plasmid in a publication.

Also, please include the text "Addgene plasmid 13776" in your Materials and Methods section. This information allows Addgene to create a link from the plasmid page to your publication.

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