TU#708
(Plasmid
#15277)
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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 | 15277 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbone95.77
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Backbone manufacturerAndy Fire (Stanford)
- Backbone size w/o insert (bp) 3500
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Vector typeWorm 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)DH5alpha
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Copy numberHigh Copy
Gene/Insert
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Gene/Insert nameczgfp
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Insert Size (bp)350
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Mutationleucine zipper fused to c-terminal half of gfp
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site BamHI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer n/a (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byleucine zipper sequences from Lynne Regan (Yale), vector sequences from Andy Fire (Stanford)
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.
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:
TU#708 was a gift from Martin Chalfie (Addgene plasmid # 15277 ; http://n2t.net/addgene:15277 ; RRID:Addgene_15277) -
For your References section:
Combinatorial marking of cells and organelles with reconstituted fluorescent proteins. Zhang S, Ma C, Chalfie M. Cell. 2004 Oct 1. 119(1):137-44. 10.1016/j.cell.2004.09.012 PubMed 15454087