pNM3649
(Plasmid
#154110)
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PurposeminiMos dual component RMCE landing site vector
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 154110 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepCFJ1272
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Backbone manufacturerAddgene #44486
- Backbone size w/o insert (bp) 3173
- Total vector size (bp) 11235
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Vector typeminiMos
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Selectable markersHygromycin
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 nameloxP::SEC::loxP::rpl-28p::FRT::GFP::his-58::unc-54 3'::FRT3
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SpeciesC. elegans (nematode), S. cerevisiae (budding yeast), Synthetic
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Insert Size (bp)8086
- Promoter not applicable
Cloning Information
- Cloning method Restriction Enzyme
- 5′ cloning site SpeI (destroyed during cloning)
- 3′ cloning site PstI (not destroyed)
- 5′ sequencing primer not applicable (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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A portion of this plasmid was derived from a plasmid made byThe insert was assembled using a multi-fragment Golden Gate reaction into an intermediate clone then moved into pCFJ1272 using standard restriction enzyme cloning. The insert was assembled from loxP::SEC::lopP from Addgene# 91829, rpl-28p from genomic sequences, FRT as a synthetic DNA, GFP::His-58::unc-54 from Addgene #86718, and FRT3 as a synthetic DNA. See Nonet (2020) Genetics for precise details.
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:
pNM3649 was a gift from Michael Nonet (Addgene plasmid # 154110 ; http://n2t.net/addgene:154110 ; RRID:Addgene_154110) -
For your References section:
Efficient Transgenesis in Caenorhabditis elegans Using Flp Recombinase-Mediated Cassette Exchange. Nonet ML. Genetics. 2020 Jun 8. pii: genetics.120.303388. doi: 10.1534/genetics.120.303388. 10.1534/genetics.120.303388 PubMed 32513816