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Browse > Keith Joung > pGP-FB-orig BA
Plasmid 13420: pGP-FB-orig BA
Gene/insert name: orig BA
Alternative names: original BCR-ABL three-finger array
Insert size (bp): 260
Species of gene(s): Other
Fusion proteins or tags: Gal11P
Terminal: N terminal on backbone
Vector backbone: pGP-FB  (Search Vector Database)
Type of vector: Bacterial expression
Backbone size (bp): 3483
Cloning site 5': XbaI
Site destroyed during cloning: No
Cloning site 3': BamHI
Site destroyed during cloning: No
5' Sequencing primer: GGG GGA TTT CTG TTC ATG GGG G  (List of Sequencing Primers)
Bacteria resistance: Ampicillin
High or low copy: Low Copy
Grow in standard E. coli @ 37C: No
Please specify bacterial strain for growth and growth condition: Needs strain with lacIq
Sequence:View sequence
Author's Map:View map
Plasmid Provided In:XL1 Blue
Principal Investigator:Keith Joung
Terms and Licenses:MTA

Comments: Positive control for B2H beta-galactosidase assay. Has coding sequence for �original� BCR-ABL three-finger array.

This plasmid requires a bacterial strain, such as XL1 Blue, that expresses the lacIq allele of lac repressor. This ensures repression of the strong lacUV5 promoter, which directs expression of the zinc finger-Gal11P hybrid protein.

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 12 - 35
M13_pUC_rev_primer 55 - 77
f1_origin 810 - 1116
AmpR_promoter 1309 - 1337
Orf frame 2 1379 - 2239
Ampicillin 1379 - 2239
pBR322_origin 2394 - 3013
pGEX_3_primer 3410 - 3432
ROP 3617 - 3426
Unique restriction sites

EcoRI 1
SalI 44
HindIII 351
NotI 360
EagI 360
XbaI 392
AgeI 482
PstI 630
BamHI 656
AseI 1991
NdeI 3233
PvuII 3465

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

Also, please include the text "Addgene plasmid 13420" 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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