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RAW-Lucia™ ISG-KO-IRF7 Cells

RAW-Lucia™ ISG-KO-IRF7 Cells Unit size Cat. code Docs Qty Price
Murine RAW 264.7 macrophages - IRF7 Knockout IRF-Lucia Luciferase Reporter Cells
3-7 x 10e6 cells
rawl-koirf7
+-
$1,421.00

You may also need : Normocin™ - Antimicrobial Reagent | View more associated products

IRF7 knockout reporter mouse macrophages

IRF signaling pathways in RAW-Lucia™ ISG-KO-IRF7 cells
IRF signaling pathways in RAW-Lucia™ ISG-KO-IRF7 cells

RAW-Lucia™ ISG-KO-IRF7 cells were generated from RAW-Lucia™ ISG cells through the stable gene knockout of the IRF7 gene. These cells feature an interferon regulatory factor (IRF)-inducible reporter gene. They derive from the murine RAW 264.7 macrophage cell line, which has been reported to express many pattern recognition receptors (PRRs) [1, 2]. RAW-Lucia™ ISG-KO-IRF7 and RAW-Lucia™ ISG cells can be used to study the role of IRF7 in a murine macrophage cell line by monitoring IRF-induced Lucia luciferase activity. Levels of secreted Lucia luciferase can be easily monitored using QUANTI-Luc™

Interferon regulatory receptor 7 (IRF7) is a transcription factor involved in the activation of the type I interferon (IFN) response upon pathogenic infection [3-4].  IRF7 has been implicated downstream of several pattern recognition receptors (PRRs), including TLRs, RLRs, and DNA sensors [2]. IRF7 is highly homologous to IRF3, and they can form either homo- or heterodimers, which ultimately lead to IFN production [2]. 

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Key Features:

  • Verified knockout of the IRF7 gene (PCR and DNA sequencing)
  • Functionally tested with a selection of PRR ligands and cytokines
  • Readily assessable Lucia luciferase

Applications:

  • Defining the role of IRF7 in PRR-induced signaling, or other cell signaling pathways
  • Highlighting the possible functional overlap between IRF7 and other transcriptional factors
  • Distinguishing the overlapping and differing roles of IRF7 and IRF3 in various signaling pathways

 

References

1. Lam E. et al., 2014. Adenovirus Detection by the cGAS/STING/TBK1 DNA Sensing Cascade. J Virol. 88:974-81.
2. Melchjorsen J. et al., 2005. Activation of innate defense against a paramyxovirus is mediated by RIG-I and TLR7 and TLR8 in a cell-type-specific manner. J Virol. 79:12944-51.
3. Ning, S. et al., 2011. IRF7: activation, regulation, modification and function. Genes Immun 12:399-414.
4. Perrotti, E. et al., 2013.IRF-7: an antiviral factor and beyond. Future Virol. 8(10):1007–20.

Figures

Validation of IRF7 knockout by PCR
Validation of IRF7 knockout by PCR

Figure 1. The targeted IRF7 region in RAW-Lucia™ ISG (WT) parental cells and RAW-Lucia™ KO ISG-KO-IRF7 (KO) cells was amplified by PCR. RAW-Lucia™ ISG-KO-IRF7 cells feature a frameshift deletion causing an early stop codon and inactivation of IRF7.

Functional validation of IRF7 knockout
Functional validation of IRF7 knockout

Figure 2: IRF response in RAW-Lucia™ ISG-derived cells. RAW-Lucia™ ISG and RAW‑Lucia™ ISG-KO-IRF7 cells were incubated with 1000 U/ml of murine interferon‑α (mIFN-α; IRF-Lucia positive control), mIFN-β (IRF-Lucia positive control), 1 μg/ml VACV‑70/LyoVec™ (CDS agonist), Poly(I:C)/LyoVec™ (RIG-I/MDA-5 agonist), 3p-hpRNA/LyoVec™ (RIG-I agonist), 10 μg/ml 2’3’-cGAMP (STING agonist), 1 μg/ml LPS-EB Ultrapure (TLR4 agonist). After overnight incubation, the IRF response was assessed by measuring the activity of Lucia luciferase in the supernatant using the QUANTI‑Luc™ detection reagent. Activity fold increase over non-induced cells is shown.

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Specifications

Growth Medium: DMEM, 4.5 g/l glucose, 2 mM L-glutamine, 10% (v/v) heat-inactivated fetal bovine serum, 100 U/ml penicillin, 100 μg/ml streptomycin, 100 μg/ml Normocin™

Antibiotic resistance: Zeocin®

Quality Control: 

  • Biallelic IRF7 knockout has been verified by PCR and DNA sequencing.
  • The stability for 20 passages, following thawing, has been verified. 
  • These cells are guaranteed mycoplasma-free. 
     

This product is covered by a Limited Use License (See Terms and Conditions).

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Contents

  • 3-7 x 106 RAW-Lucia™ ISG-KO-IRF7 cells in a cryovial or shipping flask
  • 1 ml of Normocin™ (50 mg/ml). Normocin™ is a formulation of three antibiotics active against mycoplasmas, bacteria, and fungi.
  • 1 ml of Zeocin® (100 mg/ml)
  • 1 pouch of QUANTI-Luc™ (Luciferase detection medium)

Shipped on dry ice (Europe, USA & Canada)

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Details

IRF7 background

Interferon regulatory factor 7 (IRF7) is a transcription factor involved in the activation of the type I interferon (IFN) response upon pathogenic infection [1, 2]. IRF7 is constitutively expressed by plasmacytoid dendritic cells (pDCs), which are known as ‘professional’ type I IFN producing cells [1]. However, in all other cell types IRF7, unlike its closest homolog IRF3, is only expressed upon pathogenic infection [1, 2]. IRF7 has been implicated downstream of several pattern recognition receptors (PRRs), such as TLRs, RLRs, and DNA sensors [2]. Upon PRR stimulation, IRF7 is phosphorylated through the action of the IKK-related kinases TBK1 and IKKε, and forms a homo- or heterodimer with IRF3, ultimately leading to IFN production [2]. Despite both IRF3 and IRF7 being required for IFN production in most immune cells, they have been shown to also have distinct and unique features. IRF7 is solely responsible for the production of IFN-α [1]. Importantly, IRF7 is part of a positive feedback regulatory loop essential for sustained IFN responses and full protective adaptive immunity [2]. Furthermore, it has been established that IRF7 is involved in other cellular functions, including the regulation of oncogenesis [1, 2].

 

1. Ning, S. et al. 2011. IRF7: activation, regulation, modification and function. Genes Immun 12:399-414.
2. Perrotti, E. et al. 2013. IRF-7: an antiviral factor and beyond. Future Virol. 8(10):1007–20.

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