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Irf4 control irf4fl fl

Manufactured by Jackson ImmunoResearch

The IRF4 control (Irf4fl/fl) is a laboratory reagent used for genetic research. It is a mouse strain with a floxed (flanked by loxP sites) Irf4 gene, which allows for conditional gene knockout studies. The core function of this product is to serve as a control for experiments involving the Irf4 gene in mouse models.

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2 protocols using irf4 control irf4fl fl

1

Influenza Infection and Immune Response

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WT C57/BL6 mice were purchased from the Jackson Laboratory; Blimp‐1 control (Prdm1fl/fl, where Prdm is PR domain 1), CD4‐Cre transgenic, CD8‐cre transgenic, IRF4 control (Irf4fl/fl), and CD45.1 congenic mice were originally from the Jackson Laboratory and bred inhouse. T‐cell‐specific Blimp‐1 cKO mice were generated through breeding CD4‐cre to Prdm1fl/fl mice. CD8 T‐cell‐specific IRF4 cKO mice were generated through breeding CD8‐cre to Irf4fl/fl mice. IFNAR1‐deficient (Ifnar1−/−) mice were originally from Dr. U. Deshmukh at the University of Virginia; Vert‐X mice were originally from Dr. C. Karp from Cincinnati Children's Hospital; STAT2‐deficient (Stat2−/−) mice were originally from Dr. C. Schindler at the Columbia University. All mice were housed in a specific pathogen‐free environment and all animal experiments were performed in accordance with protocols approved by the University of Virginia Animal Care and Use Committee (ACUC) or Indiana University Institutional Animal Care and Use Committee (IACUC). For influenza virus infection, mice were anesthetized first and then intranasally infected with Influenza A/PR8/34 strain (∼150 pfu/mouse in serum‐free IMDM media (Gibco) or PBS) as previously reported 8.
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2

Mouse Models for Influenza Research

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WT C57/BL6 mice were purchased from the Jackson Laboratory, Blimp-1 control (Prdm1fl/fl), CD4-Cre transgenic, CD8-cre transgenic, IRF4 control (Irf4fl/fl) and CD45.1 congenic mice were originally from the Jackson Laboratory and bred in house. T cell-specific Blimp-1 conditional knockout (cKO) mice were generated through breeding CD4-cre to Prdm1fl/fl mice. CD8 T cell-specific IRF4 cKO mice were generated through breeding CD8-cre to Irf4fl/fl mice. IFNAR1-deficient (Ifnar1−/−) mice were originally from Dr. U. Deshmukh at the University of Virginia; Vert-X mice were originally from Dr. C. Karp from Cincinnati Children’s Hospital; STAT2-deficient (Stat2−/−) mice were originally from Dr. C. Schindler at the Columbia University. All mice were housed in a specific pathogen-free environment and all animal experiments were performed in accordance with protocols approved by the University of Virginia Animal Care and Use Committee (ACUC) or Indiana University Institutional Animal Care and Use Committee (IACUC). For influenza virus infection, mice were anesthetized first and then intranasally infected with Influenza A/PR8/34 strain (~150 pfu/mouse in serum-free IMDM media (Gibco) or PBS) as previously reported (8 (link)).
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