pJCC_075 AsCas12a D908A
(Plasmid
#171668)
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PurposeFor bacterial expression of AsCas12a D908A (RuvC-inactivating mutation) with an N-terminal His-MBP tag
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 171668 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonep2CT
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Backbone manufacturerUC Berkeley MacroLab
- Backbone size w/o insert (bp) 5969
- Total vector size (bp) 9890
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Vector typeBacterial Expression
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 nameAsCas12a D908A
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Alt nameAsCpf1 D908A
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SpeciesAcidaminococcus sp.
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Insert Size (bp)3921
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Mutationchanged aspartate 908 to alanine
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Tags
/ Fusion Proteins
- 10X His (N terminal on backbone)
- maltose-binding protein (N terminal on backbone)
- TEV protease cleavage site (N terminal on backbone)
Resource Information
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Supplemental Documents
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A portion of this plasmid was derived from a plasmid made byAddgene plasmid 113430 (pMBP-AsCas12a)
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Article 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:
pJCC_075 AsCas12a D908A was a gift from Jennifer Doudna (Addgene plasmid # 171668 ; http://n2t.net/addgene:171668 ; RRID:Addgene_171668) -
For your References section:
CRISPR-Cas12a exploits R-loop asymmetry to form double-strand breaks. Cofsky JC, Karandur D, Huang CJ, Witte IP, Kuriyan J, Doudna JA. Elife. 2020 Jun 10;9. pii: 55143. doi: 10.7554/eLife.55143. 10.7554/eLife.55143 PubMed 32519675