pTGFP-T7-Hha10comp
(Plasmid
#65428)
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Purpose(Empty Backbone) Competitor vector for transcriptional mutagenesis assay
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 65428 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepTurboGFPN
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Backbone manufacturerEvroGen
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Copy numberUnknown
Resource Information
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A portion of this plasmid was derived from a plasmid made byProf. Timothy R. O'Connor (City of Hope) provided the original vector, i.e., pTGFP-Hha10, which were modified from pTurboGFPN plasmid (EvroGen, San Diego) . (Pubmed ID: 17507378).
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 pTGFP-Hha10 vector was used to generate the competitor vector, i.e., pTGFP-T7-Hha10comp.
Note: Addgene's quality control sequencing finds a T18N amino acid residue substitution in TurboGFP. This residue change is not thought to affect plasmid function for transcriptional mutagenesis assay.
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:
pTGFP-T7-Hha10comp was a gift from Yinsheng Wang (Addgene plasmid # 65428 ; http://n2t.net/addgene:65428 ; RRID:Addgene_65428) -
For your References section:
Quantitative measurement of transcriptional inhibition and mutagenesis induced by site-specifically incorporated DNA lesions in vitro and in vivo. You C, Wang Y. Nat Protoc. 2015 Sep;10(9):1389-406. doi: 10.1038/nprot.2015.094. Epub 2015 Aug 20. 10.1038/nprot.2015.094 PubMed 26292071