pKSB-618 U6-sgRNA2/3 GGAA AACA
(Plasmid
#173674)
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Purpose(Empty Backbone) To clone and express a gRNA in Anopheles
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 173674 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backbonepBluescript II KS +
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Backbone manufacturerStratagene
- Backbone size (bp) 3000
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Modifications to backboneBsaI restriction site was mutated. U6 promoter from Anopheles gambiae AGAP013557 drives expression of a classical gRNA template (Jinek et al., 2012) in which a specific gRNA protospacer sequence can be cloned using two BbsI restrictions sites.
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Vector typeInsect Expression, CRISPR
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
Cloning Information
- Cloning method Restriction Enzyme
- 5′ sequencing primer M13R
- 3′ sequencing primer M13F (Common Sequencing Primers)
Resource Information
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Supplemental Documents
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
U6 promoter from Anopheles gambiae AGAP013557 drives expression of a classical gRNA template (Jinek et al., 2012) in which a specific gRNA protospacer sequence can be cloned using two BbsI restrictions sites.
This plasmid is part of a kit to assemble a multiple-gRNA expression vector by Golden Gate Cloning for mutagenesis in Anopheles mosquitoes.
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:
pKSB-618 U6-sgRNA2/3 GGAA AACA was a gift from Eric Marois (Addgene plasmid # 173674 ; http://n2t.net/addgene:173674 ; RRID:Addgene_173674)