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Browse > Connie Cepko > Matsuda et al > pCAG-GFP
Plasmid 11150: pCAG-GFP
Gene/insert name: EGFP from Aequorea victoria
Alternative names: GFP
green fluorescent protein
Insert size (bp): 772
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)
3' Sequencing primer: EGFP-N
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: EGFP 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

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
EGFP_N_primer 1835 - 1814
EGFP 1769 - 2485
ORF frame 2 1769 - 2488
ORF frame 1 1642 - 2622
ORF frame 2 2626 - 1706
EGFP_C_primer 2422 - 2443
rb_glob_PA_terminator 2507 - 3008
M13_reverse_primer 3068 - 3050
M13_pUC_rev_primer 3089 - 3067
lac_promoter 3132 - 3103
SV40_origin 3273 - 3350
SV40_promoter 3238 - 3417
SV40pro_F_primer 3335 - 3354
SV40_PA_terminator 3431 - 3562
EBV_rev_primer 3519 - 3538
pBR322_origin 4405 - 3786
ORF frame 3 5420 - 4560
Ampicillin 5420 - 4560
AmpR_promoter 5490 - 5462
Unique restriction sites

SpeI 18
XbaI 1623
EcoRI 1719
KpnI 1739
SmaI 1748
AgeI 1756
NotI 2491
MscI 2543
BglII 2572
HindIII 3036
StuI 3406
FspI 4855

Article: Electroporation and RNA interference in the rodent retina in vivo and in vitro. Matsuda T et al. (Proc Natl Acad Sci U S A. 2004 Jan 6. 101(1):16-22. 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 11150" 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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