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Browse > Geoff Wahl > Wong et al > pL3-TRE-MCS-polyA-2L
Price: $65.00
 

 

This is commonly
requested with
RV-L3-HyTK-2L
pL3-TRE-LucGFP- 2L
Plasmid 11719: pL3-TRE-MCS-polyA-2L
Gene/insert name: None
Insert size (bp): Unknown
Vector backbone: None
(Search Vector Database)
Type of vector: Mammalian expression,Cre/Lox
Backbone size (bp): 4706
5' Sequencing primer: See map  (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: TetO sites, MCS, and polyA was cloned from pTRE2 (BD Bioscience) into the backbone.
Sequence:View sequence
Plasmid Provided In:DH5a
Principal Investigator:Geoff Wahl
Terms and Licenses:MTA, Tet Systems LULL

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

Click on map to enlarge

Selected features
pGEX_3_primer 51 - 29
lacZ_a 398 - 250
M13_pUC_fwd_primer 364 - 386
M13_forward20_primer 379 - 395
M13_forward20_primer 428 - 444
loxP 510 - 477
loxP 477 - 510
TRE 527 - 844
pCEP_fwd_primer 877 - 896
LNCX_primer 879 - 903
CMV2_promoter 846 - 965
bGlob_int 1080 - 1652
rb_glob_PA_terminator 1704 - 2217
loxP 2418 - 2451
M13_reverse_primer 2499 - 2481
M13_pUC_rev_primer 2520 - 2498
lac_promoter 2563 - 2534
pBR322_origin 3491 - 2872
ORF frame 1 4506 - 3646
Ampicillin 4506 - 3646
AmpR_promoter 4576 - 4548
Unique restriction sites

NarI 236
XhoI 527
StuI 865
SacII 969
BamHI 997
NheI 1021
NotI 1028
EcoRV 1055
NcoI 1196
ApaI 1611
MscI 1752
BglII 1781
PstI 2459
AatII 4641

Article: Reproducible doxycycline-inducible transgene expression at specific loci generated by Cre-recombinase mediated cassette exchange. Wong ET et al. (Nucleic Acids Res. 2005 . 33(17):e147. 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 11719" 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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