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PurposeExpresses nuclear-targeted human actin, with an mCherry expression reporter after a P2A protease cleavage site, on a CMV promoter
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Depositing Lab
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Depositing OrganizationUniversity of California, San Francisco (UCSF)
Located in United States of America -
Citations
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Sequence Information
Ordering
| Item | Catalog # | Description | Quantity | Price (USD) | |
|---|---|---|---|---|---|
| Plasmid | 58475 | Standard format: Plasmid sent in bacteria as agar stab | 1 | $94 | |
| DNA | 58475-D50 | 50 μg of DNA in Tris buffer | $495 | ||
| DNA | 58475-D100 | 100 μg of DNA in Tris buffer | $585 | ||
Backbone
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Vector backbonemCherry-C1
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Backbone manufacturerClontech
- Backbone size w/o insert (bp) 4700
- Total vector size (bp) 5994
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Vector typeMammalian Expression
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Selectable markersNeomycin (select with G418)
Growth in Bacteria
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Bacterial Resistance(s)Kanamycin, 50 μg/mL
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Growth Temperature37°C
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Growth Strain(s)Top10
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Copy numberHigh Copy
Gene/Insert 1
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Gene/Insert namebeta actin
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SpeciesH. sapiens (human)
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Insert Size (bp)1125
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GenBank IDNM_001101.3
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Entrez GeneACTB (a.k.a. BKRNS, BNS, BRWS1, CSMH, DDS1, PS1TP5BP1, THC8)
- Promoter CMV
Cloning Information for Gene/Insert 1
- Cloning method Ligation Independent Cloning
- 5′ sequencing primer CMV Forward
- 3′ sequencing primer mCherry Reverse
- (Common Sequencing Primers)
Gene/Insert 2
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Gene/Insert name3XNLS
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Alt namenuclear localization signal
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SpeciesSV40 virus
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Insert Size (bp)72
- Promoter CMV
Cloning Information for Gene/Insert 2
- Cloning method Ligation Independent Cloning
- 5′ sequencing primer actin Forward
- 3′ sequencing primer mCherry Reverse
- (Common Sequencing Primers)
Gene/Insert 3
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Gene/Insert nameP2A cleavage site
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Alt name2A Peptide Derived from Porcine Teschovirus-1
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SpeciesPorcine Teschovirus-1
- Promoter CMV
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Tag
/ Fusion Protein
- mCherry (C terminal on insert)
Cloning Information for Gene/Insert 3
- Cloning method Ligation Independent Cloning
- 5′ sequencing primer actin Forward
- 3′ sequencing primer mCherry Reverse
- (Common Sequencing Primers)
Resource Information
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A portion of this plasmid was derived from a plasmid made byP2A peptide and 3X NLS (with stop codons) were inserted into the pmCherry-C1 backbone via GenScript's custom cloning services. Human actin was cloned from cDNA using Gibson cloning into an NLS-P2A-mCherry backbone.
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.
DNA (Catalog # 58475-D50)
Purpose
Ready-to-use, high-purity DNA prep. DNA aliquots are suitable for use in mammalian cell transfections and other molecular biology applications.
Delivery
- Amount 50 μg
- Concentration 1 μg/μL
- Pricing $495 USD
- Storage 4 ℃ (short-term) or -20 ℃ (long-term)
Terms and Licenses
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Academic/Nonprofit Terms
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Industry Terms
- Not Available to Industry
Quality Control
Every DNA prep is verified by next-generation sequencing, confirming plasmid identity, sequence integrity, and absence of DNA contaminants. Concentration is confirmed to be within ±2.5% of the stated concentration.
Our production process has been validated to consistently yield endotoxin levels below 1.0 EU/μg. Individual lots are not tested for endotoxin.
DNA (Catalog # 58475-D100)
Purpose
Ready-to-use, high-purity DNA prep. DNA aliquots are suitable for use in mammalian cell transfections and other molecular biology applications.
Delivery
- Amount 100 μg
- Concentration 1 μg/μL
- Pricing $585 USD
- Storage 4 ℃ (short-term) or -20 ℃ (long-term)
Terms and Licenses
-
Academic/Nonprofit Terms
-
Industry Terms
- Not Available to Industry
Quality Control
Every DNA prep is verified by next-generation sequencing, confirming plasmid identity, sequence integrity, and absence of DNA contaminants. Concentration is confirmed to be within ±2.5% of the stated concentration.
Our production process has been validated to consistently yield endotoxin levels below 1.0 EU/μg. Individual lots are not tested for endotoxin.
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:
pmCherry-C1 actin-3XNLS P2A mCherry was a gift from Dyche Mullins (Addgene plasmid # 58475 ; http://n2t.net/addgene:58475 ; RRID:Addgene_58475) -
For your References section:
DNA damage induces nuclear actin filament assembly by formin-2 and Spire-1/2 that promotes efficient DNA repair. Belin BJ, Lee T, Mullins RD. Elife. 2015 Aug 19;4. doi: 10.7554/eLife.07735. 10.7554/eLife.07735 PubMed 26287480