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PurposeCRISPR-dCas9-Mxi1 vector for Yarrowia lipolytica, expressing dCas9-Mxi1 and AvrII site for sgRNA insertion
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 91248 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepUC19
- Backbone size w/o insert (bp) 2623
- Total vector size (bp) 11975
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Vector typeYeast Expression, CRISPR, Synthetic Biology
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Selectable markersLEU2
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 1
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Gene/Insert nameCodon optimized dCas9-Mxi1
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SpeciesSynthetic
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Insert Size (bp)4311
- Promoter UAS1B8-TEF(136)
Cloning Information for Gene/Insert 1
- Cloning method Restriction Enzyme
- 5′ cloning site BssHII (not destroyed)
- 3′ cloning site NheI (not destroyed)
- 5′ sequencing primer GTAAAACGACGGCCAGT
- 3′ sequencing primer CAGGAAACAGCTATGAC (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert namesgRNA expression cassette
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SpeciesSynthetic
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Insert Size (bp)525
- Promoter SCR1'-tRNA
Cloning Information for Gene/Insert 2
- Cloning method Gibson Cloning
- 5′ sequencing primer GCATTTATCAGGGTTATTGTCTCATGAG
- 3′ sequencing primer CACGAGCAGCTTGCCTATG (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byAddgene material #44380 (UAS1B8-TEF promoter) is used to express Cas9
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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.
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:
pCRISPRi_Mxi1_yl was a gift from Ian Wheeldon (Addgene plasmid # 91248 ; http://n2t.net/addgene:91248 ; RRID:Addgene_91248) -
For your References section:
CRISPRi repression of nonhomologous end-joining for enhanced genome engineering via homologous recombination in Yarrowia lipolytica. Schwartz C, Frogue K, Ramesh A, Misa J, Wheeldon I. Biotechnol Bioeng. 2017 Aug 19. doi: 10.1002/bit.26404. 10.1002/bit.26404 PubMed 28832943