pMLS236
(Plasmid
#73684)
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PurposeSapTrap 3-site Destination vector for internal GFP tagging with embedded Cbr-unc-119 selectable marker
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 73684 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepDONR221
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Backbone manufacturerThermo Fisher
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Vector typeWorm Expression, Cre/Lox, CRISPR
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Selectable markersCbr-unc-119
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 nameGFP + Cbr-unc-119
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SpeciesSynthetic
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Tag
/ Fusion Protein
- GFP
Cloning Information
- Cloning method Unknown
- 5′ sequencing primer M13 (-21) Forward
- 3′ sequencing primer M13 Reverse (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 PU6::sgRNA cassette was derived from the PU6::sgRNA cassette in Addgene plasmid #46169 from John Calarco.
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
Also encodes PU6::sgRNA cassette; The sgRNA targeting sequence can be sequenced with oMLS471: 5'-TCCAAGAACTCGTACAAAAATGCTC
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:
pMLS236 was a gift from Erik Jorgensen (Addgene plasmid # 73684 ; http://n2t.net/addgene:73684 ; RRID:Addgene_73684) -
For your References section:
SapTrap, a Toolkit for High-Throughput CRISPR/Cas9 Gene Modification in Caenorhabditis elegans. Schwartz ML, Jorgensen EM. Genetics. 2016 Feb 2. pii: genetics.115.184275. 10.1534/genetics.115.184275 PubMed 26837755