pDEST-APIC-LexAGAD
(Plasmid
#112807)
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Purpose(Empty Backbone) gateway cloning destination vector to express enhancer driven LexAGAD in Drosophila
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 112807 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepAPIC
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Vector typeBacterial Expression
Growth in Bacteria
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Bacterial Resistance(s)Chloramphenicol and Ampicillin, 25 & 100 μg/mL
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Growth Temperature37°C
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Growth Strain(s)ccdB Survival
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameNone
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
synthetic LexAGAD size is 2850 bp
For more information about the Han Lab Drosophila Transgenic Vectors, please visit: https://han.wicmb.cornell.edu/han-lab-drosophila-transgenic-vectors/.
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:
pDEST-APIC-LexAGAD was a gift from Chun Han (Addgene plasmid # 112807 ; http://n2t.net/addgene:112807 ; RRID:Addgene_112807) -
For your References section:
Dendritic space-filling requires a neuronal type-specific extracellular permissive signal in Drosophila. Poe AR, Tang L, Wang B, Li Y, Sapar ML, Han C. Proc Natl Acad Sci U S A. 2017 Sep 19;114(38):E8062-E8071. doi: 10.1073/pnas.1707467114. Epub 2017 Sep 5. 10.1073/pnas.1707467114 PubMed 28874572