pCAG-i53-bpA-EF1BFP
(Plasmid
#111145)
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PurposeExpression of i53 and a BFP reporter in mammalian cells
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Depositing Lab
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Sequence Information
Ordering
Item | Catalog # | Description | Quantity | Price (USD) | |
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Plasmid | 111145 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $85 |
Backbone
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Vector backboneBluescript
- Total vector size (bp) 7175
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Vector typeMammalian 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 1
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Gene/Insert namei53
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SpeciesSynthetic
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Insert Size (bp)225
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Mutationhuman Ubiquitin, contains 8 point mutations
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GenBank IDAAA72608.1
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Entrez GenemutL (a.k.a. HLAC_RS03120, Hlac_0629)
- Promoter CAG promoter
Cloning Information for Gene/Insert 1
- Cloning method Restriction Enzyme
- 5′ cloning site PacI (not destroyed)
- 3′ cloning site MluI (not destroyed)
- 5′ sequencing primer M13 reverse
- 3′ sequencing primer M13 forward (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert nameBFP
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SpeciesSynthetic
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Insert Size (bp)720
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Entrez GeneBFP
- Promoter EF1
Cloning Information for Gene/Insert 2
- Cloning method Restriction Enzyme
- 5′ cloning site AsiSI (not destroyed)
- 3′ cloning site EcoRI (not destroyed)
- 5′ sequencing primer M13 reverse
- 3′ sequencing primer M13 forward (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 byAmplified from Addgene plasmid 74939 deposited by Daniel Durocher
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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.
Depositor Comments
Amplified from Addgene plasmid 74939 deposited by Daniel Durocher.
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:
pCAG-i53-bpA-EF1BFP was a gift from Ralf Kuehn (Addgene plasmid # 111145 ; http://n2t.net/addgene:111145 ; RRID:Addgene_111145) -
For your References section:
Efficient Gene Editing of Human Induced Pluripotent Stem Cells Using CRISPR/Cas9. Yumlu S, Bashir S, Stumm J, Kuhn R. Methods Mol Biol. 2019;1961:137-151. doi: 10.1007/978-1-4939-9170-9_10. 10.1007/978-1-4939-9170-9_10 PubMed 30912045