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Purpose(Empty Backbone) Bacterial expression of Cas9 nuclease and RecAb recombination system in Acinetobacter baumannii
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 121998 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepMMB67EH
- Backbone size (bp) 16599
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Vector typeBacterial Expression, CRISPR
Growth in Bacteria
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Bacterial Resistance(s)Apramycin, 25 μg/mL
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Growth Temperature37°C
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Growth Strain(s)DH5alpha
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Growth instructionsSelectable Marker: 100 μg/mL apramycin in both E.coli DH5alpha and Acinetobacter baumannii. Plasmid is prone to recombination, test 2-3 colonies.
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Copy numberLow Copy
Cloning Information
- Cloning method Gibson Cloning
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
Please note that the plasmid is prone to recombination between the duplicate tac promoter-lac operator. Addgene recommends that you test 2-3 colonies via digest or sequencing to confirm that the full 16.6kb plasmid was selected.
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:
pCasAb-apr was a gift from Quanjiang Ji (Addgene plasmid # 121998 ; http://n2t.net/addgene:121998 ; RRID:Addgene_121998) -
For your References section:
A Highly Efficient CRISPR-Cas9-Based Genome Engineering Platform in Acinetobacter baumannii to Understand the H2O2-Sensing Mechanism of OxyR. Wang Y, Wang Z, Chen Y, Hua X, Yu Y, Ji Q. Cell Chem Biol. 2019 Sep 17. pii: S2451-9456(19)30277-6. doi: 10.1016/j.chembiol.2019.09.003. 10.1016/j.chembiol.2019.09.003 PubMed 31548010