YIplac211-SEC7-mCherry2Bx6
(Plasmid
#105267)
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PurposePlasmid for pop-in/pop-out replacement of Sec7 with Sec7-mCherry2Bx6.
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 105267 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneYIplac211
- Backbone size w/o insert (bp) 3797
- Total vector size (bp) 10410
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Vector typeYeast Expression
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Selectable markersURA3
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 nameSec7 portion
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SpeciesS. cerevisiae (budding yeast)
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Entrez GeneSEC7 (a.k.a. YDR170C)
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Tag
/ Fusion Protein
- mCherry2Bx6 (C terminal on insert)
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site EcoRI (not destroyed)
- 3′ cloning site SphI (not destroyed)
- 5′ sequencing primer M13 FORWARD
- 3′ sequencing primer M13 REVERSE (Common Sequencing Primers)
Resource Information
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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
Addgene's quality control identified a frameshift at Q266 of URA3. The depositing lab states that this mutation should not affect selection.
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:
YIplac211-SEC7-mCherry2Bx6 was a gift from Benjamin Glick (Addgene plasmid # 105267 ; http://n2t.net/addgene:105267 ; RRID:Addgene_105267) -
For your References section:
Budding Yeast Has a Minimal Endomembrane System. Day KJ, Casler JC, Glick BS. Dev Cell. 2018 Jan 8;44(1):56-72.e4. doi: 10.1016/j.devcel.2017.12.014. Epub 2018 Jan 8. 10.1016/j.devcel.2017.12.014 PubMed 29316441