PBDGTV
(Plasmid
#100859)
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Purpose(Empty Backbone) A piggyBac transposon based dual directional gene trap vector, in which, the mutagens are two non-selectable gene-trap cassettes in opposite orientations.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 100859 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepBR322
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Vector typeMammalian Expression
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Selectable markersPuromycin
Growth in Bacteria
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Bacterial Resistance(s)Ampicillin, 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberLow Copy
Cloning Information
- Cloning method Restriction Enzyme
Resource Information
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Supplemental Documents
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Trademarks:
- Zeocin® is an InvivoGen trademark.
Depositor Comments
The plasmid PBDGTV is a piggyBac transposon based dual directional gene trap vector, in which, the mutagens are two non-selectable gene-trap cassettes in opposite orientations. This vector can be used for selection of mutant clones independent of expression of the target gene. In this vector, a selection marker gene, puroTK, driven by the mouse phosphoglyceratekinase promoter (PGK), allows selection for PB integration into the chromosome using puromycin.
These plasmids were created by your colleagues. Please acknowledge the Principal Investigator, cite the article in which the plasmids were described, and include Addgene in the Materials and Methods of your future publications.
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For your Materials & Methods section:
PBDGTV was a gift from Yue Huang (Addgene plasmid # 100859 ; http://n2t.net/addgene:100859 ; RRID:Addgene_100859) -
For your References section:
Arrayed mutant haploid embryonic stem cell libraries facilitate phenotype-driven genetic screens. Liu G, Wang X, Liu Y, Zhang M, Cai T, Shen Z, Jia Y, Huang Y. Nucleic Acids Res. 2017 Sep 28. doi: 10.1093/nar/gkx857. 10.1093/nar/gkx857 PubMed 29036617