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Browse > Chaoyang Zeng > Article > pGT2
Plasmid 13056: pGT2
Gene/insert name: none
Insert size (bp): Unknown
Vector backbone: pGT2
(Search Vector Database)
Type of vector: Bacterial expression
Backbone size (bp): 3267
Cloning site 5': XcmI, HindIII, StyI, BspEI, EcoRV
Site destroyed during cloning: No
Cloning site 3': XcmI, SacI, SpeI, NotI, EcoRI, AatII
Site destroyed during cloning: No
5' Sequencing primer: M13/pUC Reverse  (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: Modified from pGFPTA (Husimi et al, 2000)
Sequence:View sequence
Author's Map:View map
Principal Investigator:Chaoyang Zeng
Terms and Licenses:MTA

Comments: pGT2 is an XcmI generated T-vector bearing GFP marker optimized for direct cloning. Colonies with insert are selected by GFP inactivation.

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

Click on map to enlarge

Selected features
lac_promoter 88 - 117
M13_pUC_rev_primer 131 - 153
M13_reverse_primer 152 - 170
GFP_R_primer 292 - 264
GFPfusionREV_primer 327 - 308
ORF frame 3 162 - 956
GFP_cyc3(variant) 234 - 941
GFP_F_primer 887 - 907
AmpR_promoter 1111 - 1139
ORF frame 2 1181 - 2041
Ampicillin 1181 - 2041
pBR322_origin 2196 - 2815
pGEX_3_primer 3212 - 3234
Unique restriction sites

HindIII 179
XbaI 203
NcoI 399
MscI 404
EcoRV 526
XhoI 654
SacI 940
SpeI 952
NotI 963
EagI 963
EcoRI 970
AatII 1049
FspI 1745
PvuII 3267

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

Also, please include the text "Addgene plasmid 13056" 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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