pEGFP-C1 RPEL1-EGFP-3XNLS
(Plasmid #58469)

• Purpose: Expresses a nuclear-targeted monomeric actin reporter, consisting of the RPEL1 domain from MAL/MRTF, on a CMV promoter
• Depositing Lab: Dyche Mullins
• Publication: Belin et al Mol Biol Cell. 2013 Apr;24(7):982-94. doi: 10.1091/mbc.E12-09-0685. Epub 2013 Feb 27.

Backbone

• Vector backbone: pEGFP-C1
• Backbone manufacturer: Clontech
• Backbone size w/o insert (bp): 4686
• Total vector size (bp): 4797
• Vector type: Mammalian Expression
• Selectable markers: Neomycin (select with G418)

Growth in Bacteria

• Bacterial Resistance(s): Kanamycin, 50 μg/mL
• Growth Temperature: 37°C
• Growth Strain(s): Top10
• Copy number: High Copy

Gene/Insert 1

• Gene/Insert name: MRTF-A RPEL1
• Species: M. musculus (mouse), Synthetic
• Insert Size (bp): 99
• GenBank ID: AF532597
• Entrez Gene: Mrtfa (a.k.a. AMKL, Bsac, Mal, Mkl1, Mrtf-A)
• Promoter: CMV
• Tag / Fusion Protein:
  • EGFP (C terminal on insert)

Cloning Information for Gene/Insert 1

• Cloning method: Restriction Enzyme
• 5′ cloning site: NheI (not destroyed)
• 3′ cloning site: AgeI (not destroyed)
• 5′ sequencing primer: CMV Forward
• 3′ sequencing primer: EGFP Reverse

Gene/Insert 2

• Gene/Insert name: 3X NLS with 3X stop codons
• Species: SV40 virus
• Insert Size (bp): 72
• Promoter: CMV
• Tag / Fusion Protein:
  • EGFP (N terminal on insert)

Cloning Information for Gene/Insert 2

• Cloning method: Restriction Enzyme
• 5′ cloning site: HindIII (not destroyed)
• 3′ cloning site: KpnI (not destroyed)
• 5′ sequencing primer: EGFP Forward
• 3′ sequencing primer: SV40 polyA Reverse

Resource Information

• A portion of this plasmid was derived from a plasmid made by: 3X NLS (with stop codons) was cloned by insertion of annealed primers with flanking restriction sites.
• Article Citing this Plasmid:
  • 1 Reference

Terms and Licenses

• Academic/Nonprofit Terms:
  • UBMTA
• Industry Terms:
  • Not Available to Industry