pDEST-APIGH
(Plasmid
#112804)
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Purpose(Empty Backbone) gateway cloning destination vector to express enhancer driven Gal4 in Drosophila
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Depositing Labs
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 112804 | 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)Ampicillin, 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
S. cerevisiae (budding yeast) Gal 4 size is 2646 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-APIGH was a gift from Chun Han & Yuh-Nung Jan (Addgene plasmid # 112804 ; http://n2t.net/addgene:112804 ; RRID:Addgene_112804) -
For your References section:
Integrins regulate repulsion-mediated dendritic patterning of drosophila sensory neurons by restricting dendrites in a 2D space. Han C, Wang D, Soba P, Zhu S, Lin X, Jan LY, Jan YN. Neuron. 2012 Jan 12;73(1):64-78. doi: 10.1016/j.neuron.2011.10.036. 10.1016/j.neuron.2011.10.036 PubMed 22243747