pmr101A-cPr-mCherry (ErmR)
(Plasmid #177206)

• Purpose: Plasmid with p15A origin for constitutive mCherry expression in E. coli
• Depositing Lab: Alexey Merz
• Publication: Plasmids with p15A origin for constitutive fluorescent protein expression in E. coli (unpublished)

Backbone

• Vector backbone: pmr101A
• Total vector size (bp): 4225
• Vector type: Bacterial Expression

Growth in Bacteria

• Bacterial Resistance(s): Erythromycin, 200 μg/mL
• Growth Temperature: 37°C
• Growth Strain(s): DH5alpha
• Copy number: Low Copy

Gene/Insert

• Gene/Insert name: mCherry
• Species: Discosoma
• Insert Size (bp): 711
• GenBank ID: AY678264.1
• Promoter: Synthetic constitutive promoter

Cloning Information

• Cloning method: Gibson Cloning
• 5′ sequencing primer: pmr101A forward mapping primer
• 3′ sequencing primer: T7 Term

Resource Information

• A portion of this plasmid was derived from a plasmid made by: Shaner, N., Campbell, R., Steinbach, P. et al. Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein. Nat Biotechnol 22, 1567–1572 (2004). https://doi.org/10.1038/nbt1037

Terms and Licenses

• Academic/Nonprofit Terms:
  • UBMTA
  • Takara Bio Limited Use Label License (formerly Clontech)
• Industry Terms:
  • Not Available to Industry

Depositor Comments

Braatsch S, Helmark S, Kranz H, Koebmann B, Jensen PR. Escherichia coli strains with promoter libraries constructed by Red/ET recombination pave the way for transcriptional fine-tuning. Biotechniques. 2008 Sep;45(3):335-7. doi: 10.2144/000112907. PMID: 18778259.