CMV mRuby3-Synapsin1a
(Plasmid
#187896)
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PurposeFor labeling pre-synaptic terminals
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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 | 187896 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepEGFP-C1 vector
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Backbone manufacturerClontech, Palo Alto, California
- Backbone size w/o insert (bp) 3998
- Total vector size (bp) 6839
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Modifications to backboneA plasmid to express mRuby-synapsin was generated by removing GFP from GFP-synapsin (Chi et al., 2001) using restriction sites AgeI and BglII, and substituting it in frame with mRuby obtained from pKanCMV-mRuby3-18aa-actin, which was a gift from Michael Lin (Addgene plasmid # 74255).
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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 numberHigh Copy
Gene/Insert
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Gene/Insert nameSynapsin1a
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SpeciesR. norvegicus (rat)
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Insert Size (bp)2115
- Promoter CMV
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Tag
/ Fusion Protein
- mRuby3 (N terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site AgeI (not destroyed)
- 3′ cloning site BglII (not destroyed)
- 5′ sequencing primer CMV-F
- 3′ sequencing primer SV40pA-R (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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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
F255Y and S304A mutations in Synapsin1a insert do not affect plasmid function.
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:
CMV mRuby3-Synapsin1a was a gift from Timothy Ryan (Addgene plasmid # 187896 ; http://n2t.net/addgene:187896 ; RRID:Addgene_187896)