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R26r eyfp

Manufactured by Jackson ImmunoResearch
Sourced in United States, Sweden, Montenegro

The R26R-EYFP is a reporter mouse line that expresses the enhanced yellow fluorescent protein (EYFP) upon Cre-mediated recombination. This line allows for the visualization of Cre-expressing cells and their progeny through the expression of EYFP.

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22 protocols using r26r eyfp

1

Krt5-CreERT2:R26R-EYFP Lineage Tracing

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All the experiments were approved by the ethical committee from the university and conform with regulatory standards (LA1230406, project 666N). Mice were bred and maintained under pathogen-free conditions in a certified animal facility in accordance with the European guidelines. Adult (8-week-old) wild-type CD1 mice or Krt8-YFP knock-in mice (18 (link)) were used for sequencing and histology. Krt5-CreERT2 knock-in mice (the Jackson Laboratory, stock no. 029155; RRID:IMSR_JAX:029155) were crossed with R26R-EYFP (the Jackson Laboratory, stock no. 006148; RRID:IMSR_JAX:006148) to generate Krt5-CreERT2:R26R-EYFP (K5:RYFP) mice. For lineage tracing experiments, 10 or 0.25 mg of TAM resuspended in sunflower oil was injected intraperitoneally to 8-week-old K5:RYFP mice, and the expression of the YFP was analyzed in esophagi up to 4 weeks after TAM administration. In all the experiments, littermates of the same sex were randomly assigned to experimental groups.
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2

Genotyping and Mouse Lines for Lung Research

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Development and genotyping information for mouse lines SftpcCreERT2, Fgfr2fl/fl (Jackson Laboratory stock # 007569), R26REYFP (Jackson Laboratory stock # 007903), Ai14(RCL-tdT)-D (R26RtdTomato) (Jackson Laboratory stock # 007914), and Ect2fl/fl have been previously described (Chapman et al., 2011 (link); Madisen et al., 2010 (link); Windmueller et al., 2020 (link); Yu et al., 2003 (link)). Fgfr2fl/fl, R26RtdTomato, and R26REYFP mouse lines were purchased from the Jackson Laboratory. All mice were maintained on a mixed background (C57BL/6 and CD1). No obvious defects were observed in heterozygous mice, so SftpcCreERT2;Fgfr2fl/+;R26REYFP and SftpcCreERT2;Ect2fl/+;R26REYFP littermates were used as controls for all experiments except for the organoid experiments in Figure 4 where SftpcCreERT2;R26RtdTomato mice were used and the adult one month or longer influenza experiments in Figures 5C5I,6B, and 6D6I where SftpcCreERT2;R26REYFP mice, including littermates, were used. Experiments were all performed with a minimum of n = 3 mice per condition of mixed gender, and unless otherwise stated each dot on a graph represents one mouse. All procedures for animal experiments were performed under the guidance of the University of Pennsylvania Institutional Animal Care and Use Committee.
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3

Genotyping and Mouse Lines for Lung Research

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Development and genotyping information for mouse lines SftpcCreERT2, Fgfr2fl/fl (Jackson Laboratory stock # 007569), R26REYFP (Jackson Laboratory stock # 007903), Ai14(RCL-tdT)-D (R26RtdTomato) (Jackson Laboratory stock # 007914), and Ect2fl/fl have been previously described (Chapman et al., 2011 (link); Madisen et al., 2010 (link); Windmueller et al., 2020 (link); Yu et al., 2003 (link)). Fgfr2fl/fl, R26RtdTomato, and R26REYFP mouse lines were purchased from the Jackson Laboratory. All mice were maintained on a mixed background (C57BL/6 and CD1). No obvious defects were observed in heterozygous mice, so SftpcCreERT2;Fgfr2fl/+;R26REYFP and SftpcCreERT2;Ect2fl/+;R26REYFP littermates were used as controls for all experiments except for the organoid experiments in Figure 4 where SftpcCreERT2;R26RtdTomato mice were used and the adult one month or longer influenza experiments in Figures 5C5I,6B, and 6D6I where SftpcCreERT2;R26REYFP mice, including littermates, were used. Experiments were all performed with a minimum of n = 3 mice per condition of mixed gender, and unless otherwise stated each dot on a graph represents one mouse. All procedures for animal experiments were performed under the guidance of the University of Pennsylvania Institutional Animal Care and Use Committee.
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4

Genetic Fate Mapping of Sox9 Cells

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All animal procedures were conducted according to the National Institutes of Health Guide for the Care and Use of Laboratory Animals and were approved by the Institutional Animal Care and Use Committee at the University of Wisconsin-Milwaukee. Sox9-cre mice, in which an IRES-Cre-pA cassette was inserted within the 3′UTR of the endogenous Sox9 gene, were a kind gift from Dr Benoit de Crombrugghe (Akiyama et al., 2005 (link)). B6.129X1-Gt(ROSA)26Sortm1(EYFP)Cos/J mice (Srinivas et al., 2001 (link)), henceforth designated as R26R-EYFP, were obtained from The Jackson Laboratory (Bar Harbor, ME, USA). Timed matings between homozygous mice from each strain were conducted to produce Sox9cre; R26R-EYFP embryos. The presence of a vaginal plug on the following morning was counted as E0.5.
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5

Mouse Genetic Models for B Cell Immunology

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CD21-Cre (Cr2-Cre, 006368), AID-Cre (Aicda-Cre, 007770), Cγ1-Cre (Ighg1-Cre, 010612), Blimp1-Cre (Prdm1-Cre, 008827), R26R-EYFP (006148), B6 (C57BL/6J, 000664), and B6 CD45.1 (002014) mice were originally purchased from Jackson Laboratory and bred/maintained in specific pathogen–free facility at Seattle Children’s Research Institute. Pik3cdE1020K/+ mice were generated in our laboratory as previously described (Wray-Dutra et al., 2018 (link)). All mice were maintained on C57BL/6 background. Male and female 10- to 14-wk-old mice were used in the experiments. Animal experiments were conducted according to the protocols approved by Institutional Animal Care and Use Committee at Seattle Children’s Research Institute.
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6

Targeting Chx10-Expressing Neurons

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All animal experiments and procedures were performed in laboratory mice (Mus musculus), carried according to the EU Directive 2010/63/EU, and approved by the Danish Animal Experiments Inspectorate (Dyreforsøgstilsynet, license no. 2017-15-0201-01172) and the local ethics committee at the University of Copenhagen.
For all behavioral experiments targeting the PPN, we used hemizygous Chx10Cre mice (same strain as previously reported7 (link),35 (link)). For targeting the vlPAG, we crossed hemizygous Chx10Cre mice with the homozygous conditional R26RChR2−EYFP line (stock no. 012569, Jackson Laboratories). For anatomical studies, we crossed hemizygous Chx10Cre mice with the homozygous conditional reporter lines R26REYFP or R26RtdTomato (stock no. 006148 and 007905, respectively, Jackson Laboratories). All experiments were performed in adult (>8 weeks) male or female mice (randomly selected, approximately 1:1) kept on a 12-h light–dark cycle with access to food and water ad libitum (housing temperature 23–24 °C, 45–65% humidity).
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7

Genotyping Fbln5 Knockout Mice

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The Fbln5+/− mice [6 (link)] were maintained on a C57BL/6J background. Mice from Fbln5+/− × Fbln5+/− crosses were genotyped by PCR using the forward primers pgk-s1 (5’-CTGCTAAAGCGCATGCTCCAGACTG-3’) and A55Gs1 (5’-CGCTTTGGGTATCAGATGGATGAAGG-3’), specific for the mutated and wild-type allele, respectively. The common reverse primer A55Ga2 (5’- AATGAGGTTGGTCACCAATGAGATCC-3’) was also used for genotyping. R26R-EYFP [15 (link)] and Wnt1-Cre [16 (link)] mice were obtained from The Jackson Laboratory. All mice were maintained in the Animal Facility of The University of Texas Medical School at Houston. The experimental protocol was reviewed and approved by the Animal Welfare Committee, the Institutional Animal Care and Use Committee of the University of Texas Health Science Center at Houston.
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8

Transgenic Mice for Fate Mapping

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The transgenic mouse line Glast-CreERT (JAX#012586), and reporter mouse lines Rosa-CAG-LSL-Sun1-GFP (JAX#021039), Rosa-CAG-LSL-tdTomato (Ai9, JAX#007909) and R26R-EYFP (JAX#006148) were purchased from The Jackson Laboratory. Hemizygous Glast-CreERT mice and homozygous reporter mice were used for breeding. Glast-CreERT;Rosa-CAG-LSL-Sun1-GFP, Glast-CreERT;Rosa-CAG-LSL-tdTomato and Glast-CreERT;R26R-EYFP fate mapping mice were PCR genotyped and confirmed by using published protocols on Jackson Laboratory. All mice were housed under controlled room temperature and a 12-h light/dark cycle with free access to water and food. Mice at postnatal five weeks of either sex were randomly assigned to different groups for all experiments. All procedures were consistent with animal protocols approved by the Institutional Animal Care and Use Committee at the Icahn School of Medicine at Mount Sinai.
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9

Genetic Mouse Models for Vascular Research

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The genetic mouse models used in this study were: Ccr2−/− (stock 004999), Nur77−/− (stock 006187), R26R-EYFP (stock 006148), Cx3cr1CreERT2 (stock 020940), and Csf1rCreEsr1 (stock 019098), purchased from Jackson Laboratories, and Plvaptm1Salm (Plvap−/−) mice (42 (link), 43 (link)). Wild type (WT) mice, C57BL/6J and C57BL/6N, were acquired from Janvier labs. All mice were kept under 22°C and 12 hours of light and 12 hours dark cycles at the animal facilities of the University of Turku (Turku, Finland). Unless stated otherwise, the animals were fed with standard pellet chow and reverse osmosis water. Only males were used in all experiments, and age-matched WT mice were used as controls in each experiment. Embryonic development was estimated considering the day of a vaginal plug as embryonic day 0.5 (E0.5). Animal experiments were conducted under the revision and approval of the Regional Animal Experiment Board in Finland, according to the 3R-principle and under Animal license numbers 6211/04.10.07/2017 and 14685/2020. All experiments were regulated according to the Finnish Act on Animal Experimentation (497/2013).
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10

Mice Strains for Immunology Research

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All animals were housed at the National Cancer Institute (NCI) animal facility under specific pathogen free (SPF) conditions and used between 8 – 10 weeks of age. All studies were performed under animal protocols approved by the NCI Animal Care and Use Committee. C57BL/6J (Stock No. 000664), 2D2 TCR transgenic mice (TCRMOG, Stock No. 00691251 (link)), Tcrb−/− (Stock No. 002118), hCD2-Cre (Stock No. 02740630 (link)), Il17a-Cre (Stock No. 01687923 (link)), B10.BR (Stock No. 004804), and R26R-EYFP (Stock No. 006148) mice were purchased from the Jackson laboratory. Egr2f/f mice were generated and previously characterized by W. J. Leonard (NHLBI)27 (link). Triple Egr1−/−Egr2ΔTEgr3−/− mice were generated by crossing hCD2-Cre (Stock No. 027406) to the germline Egr1−/−52 (link), Egr2f/f29 (link), germline Egr3−/−53 (link) mouse line, which was developed and kindly provided by D. L. Wiest (Fox Chase Cancer Center). Tbx21-ZsGreen reporter mice were generated and previously characterized by J. Zhu (NIAID)54 (link). Rorc−/− mouse line55 (link) on Bcl2l1Tg56 (link) background was generated and maintained in-house. AND TCR transgenic mice were kindly provided by A. Singer (NCI).
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