pUC19mut_circIRES5_FLuc_3HA
(Plasmid #249688)

• Purpose: This plasmid is designed to evaluate the translation efficiency of IRES5, an internal ribosome entry site derived from the Turnip crinkle virus (TCV).
• Depositing Lab: Timo Schlemmer
• Publication: Schlemmer Lab Plasmids 2025 (unpublished)

Backbone

• Vector backbone: pUC19mut
• Backbone manufacturer: Selfmade
• Backbone size w/o insert (bp): 4642
• Vector type: Bacterial Expression, Synthetic Biology

Growth in Bacteria

• Bacterial Resistance(s): Ampicillin, 100 μg/mL
• Growth Temperature: 37°C
• Growth Strain(s): NEB Stable
• Copy number: High Copy

Gene/Insert

• Gene/Insert name: IRES of Turnip crinkle virus
• Alt name: IRES5
• Species: Turnip crinkle virus/ Betacarmovirus brassicae
• Insert Size (bp): 119
• Promoter: T7 Promoter
• Tag / Fusion Protein:
  • 3xHA (C terminal on insert)

Cloning Information

• Cloning method: Golden Gate

Terms and Licenses

• Academic/Nonprofit Terms:
  • UBMTA
  • Luciferase Limited Use Label License
• Industry Terms:
  • Not Available to Industry

Depositor Comments

This plasmid is designed to evaluate the translation efficiency of IRES5, an internal ribosome entry site derived from the Turnip crinkle virus (TCV). The IRES is located upstream of the open reading frame for the p9 movement protein and is characterized by A-rich regions, a feature that appears to be well-conserved among IRESs in the Carmovirus genus, indicating their functional importance (May et al., 2017). The firefly luciferase (Fluc) reporter gene is positioned downstream of the IRES to enable quantitative analysis of translation efficiency through luciferase assays. A C-terminal 3xHA tag allows for the detection of Fluc expression via western blotting. This construct is primarily intended for comparative luciferase assays to assess the relative efficiency of different IRES elements in driving translation. Firefly luciferase downstream of IRES to asses translation efficiency.