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Purpose(Empty Backbone) Insect expression vector
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Depositing Lab
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Publication
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 17923 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 | |
Cloning Grade DNA | 17923-DNA.cg | 2 µg of cloning grade DNA in Tris buffer | 1 | $105 |
Backbone
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Vector backbonepMT-puro
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Vector typeInsect Expression ; Drosophila metallothionein gene promoter drives 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 numberUnknown
Gene/Insert
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Gene/Insert nameNone
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer MT forward (Common Sequencing Primers)
Resource Information
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Addgene Notes
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Articles Citing this Plasmid
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
Insect expression vector.
This was the empty vector used in http://www.addgene.org/pubmed/17589500
This is NOT the vector by the same name described in the Castellino lab's 2008 Cytotechnology paper.
Notes from the Sabatini lab on using this plasmid:
They did a puromycin kill curve and ended up using 2 ug/mL of puromycin for selection for S2R cells. They used 5 mM CuSO4 to induce expression of their gene 24 hours before performing the IF experiments. The metallothionein promoter is described in this link: https://www.ncbi.nlm.nih.gov/pubmed/3125519
Information for Cloning Grade DNA (Catalog # 17923-DNA.cg) ( Back to top)
Purpose
Cloning grade DNA is suitable for use in PCR, cloning reactions, or transformation into E. coli. The purity and amount is not suitable for direct transfections.
Delivery
- Amount 2 µg
- Guaranteed Concentration 100 ng/µl +/- 5 ng/µl
- Pricing $105 USD
- Storage DNA can be stored at 4℃ (short term) or -20℃ (long term).
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Quality Control
Addgene has verified this plasmid using Next Generation Sequencing. Results are available here
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:
pMT-puro was a gift from David Sabatini (Addgene plasmid # 17923 ; http://n2t.net/addgene:17923 ; RRID:Addgene_17923)