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B6.129p2 c ccr7tm1rfor j

Manufactured by Jackson ImmunoResearch
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The B6.129P2(C)-Ccr7tm1Rfor/J is a targeted mutation mouse strain. It has a disruption in the Ccr7 gene, which encodes the chemokine receptor CCR7. This receptor is involved in the migration and homing of lymphocytes.

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17 protocols using b6.129p2 c ccr7tm1rfor j

1

Transgenic Mice for Immune Studies

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FcγRIIb-deficient mice on a C57BL/6 background18 (link) were kindly provided by Jeff Ravetch (Rockefeller University, New York) and Silvia Bolland (National Institutes of Health, NIAID, Bethesda, MD) and crossed to transgenic mice expressing EGFP under the control of the human ubiquitin C promoter38 (Jackson Laboratories) or transgenic mice expressing Venus EYFP under the control of the CD11c promoter39 (obtained from M. Nussenzweig, Rockefeller University, New York, NY). C57BL/6 mice were obtained from Jackson Laboratories or from Charles River Laboratories (Margate, UK). NZB/W F1 were bred in-house from NZB and NZW mice obtained from Harlan UK. CCR7-deficient mice on a C57BL/6 background (strain B6.129P2(C)-Ccr7tm1Rfor/J, stock number 006621, live repository, aged 8 weeks old) were purchased from Jackson Laboratories. Age matched C57BL/6 JAX mice were used as controls. In all experiments, both male and female mice were used. Mice were maintained in specific-pathogen-free conditions at an Association for Assessment and Accreditation of Laboratory Animal Care-accredited animal facility at NIAID or at a Home Office-approved facility in the UK. All procedures were approved by the NIAID Animal Care and Use Committee (National Institutes of Health, Bethesda, MD) or were conducted in accordance with the United Kingdom Animals (Scientific Procedures) Act 1986.
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2

Multimodal Immune Cell Profiling

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C57BL/6J, B6.129(Cg)-Ccr2tm2.1Ifc/J (CCR2-RFP), B6.Cg-Tg(Itgax-Venus)1Mnz/J (CD11c-YFP), B6(Cg)-Tyrc−2J/J (B6 albino), B6.Cg-Zbtb46tm4.1(HBEGF)MnzTyrc−2J/J (Zbtb46-DTR), B6.129P2(C)-Ccr7tm1Rfor/J (CCR7.KO), B6.129S1-Il12btm1Jm/J (IL-12p40.KO), and B6.129S4-Ccr2tm1Ifc/J (CCR2.KO) mouse strains were obtained from The Jackson Laboratory. CD45.1+ B6.Cg-Tg(TcraTcrb)425Cbn/J (OT-II), CD45.1+ C57BL/6-Tg(TcraTcrb)1100Mjb/J (OT-I), and B6.SJL-PtprcaPepcb/BoyCrl (CD45.1+) were obtained either from donating investigators (Dr. Pamela J. Fink, University of Washington) or Charles River. CD11c-YFP animals were crossed with B6 albino mice to homozygosity, and next crossed to CCR2-RFP mice to generate a CD11c-YFP x CCR2-RFPHetrozygous dual reporter mice. CCR2-DTR mice were obtained from donating investigators (Dr. Steven F. Ziegler, Benaroya Research Institute) and with approval from the originating investigators (Drs. Tobias M. Hohl and Eric G. Pamer, Memorial Sloan-Kettering Cancer Center) (95 (link)). 6–10 week-old male and female mice were kept in specific pathogen–free conditions at an Association for Assessment and Accreditation of Laboratory Animal Care–accredited animal facility at the University of Washington, South Lake Union campus. All procedures were approved by the University of Washington Institutional Animal Care and Use Committee.
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3

Vitamin A Deficiency Mouse Models

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All animal experiments in this study were approved by the Purdue Animal Care and Use Committee. C57BL/6 mice were from Harlan. CD45.1 congenic (B6.SJL-PtprcaPepcb/BoyJ, Stock# 002014), CD90.1 congenic (B6.PL-Thy1a/CyJ, Stock# 000406), Rag1−/− (B6.129s7-Rag1tm1Mom/J, Stock# 002216), Ccr7−/− (B6.129P2(C)-Ccr7tm1Rfor/J, Stock# 006621), and Itgβ7−/− (C57BL/6-Itgb7tm1Cgn/J, Stock# 002965) mice were originally from the Jackson Laboratory. Ccr9−/− mice in the C57BL/6 background were described previously (Uehara et al., 2002 ). All strains were kept at Purdue for at least 12 months. VAD and VAN Rag1−/− or C57BL/6 mice were prepared by keeping mice on custom research diets (0 and 2,500 IU/kg of retinyl acetate respectively for VAD and VAN, Harlan Teklad diets, Indianapolis, IN) immediately following birth and after weaning until they are 11–12 weeks of age.
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4

Immunophenotyping of Transgenic Mouse Models

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C57BL/6J (Stock No: 000664), B6.FVB-1700016L21RikTg (Itgax-DTR/EGFP)57Lan/J) (CD11c-DTR, Stock No: 004509) (37 (link)), C57BL/6-Tg(TcraTcrb)1100Mjb/J (OT-1, Stock No: 003831) (80 (link)), and B6.129P2(C)-Ccr7tm1Rfor/J (CCR7−/−, Stock No: 006621) (81 (link)) mice were obtained from Jackson Laboratories and bred and maintained in the barrier facility at the University of Texas Southwestern Medical Center. All animals were kept on a 12-hour light-dark cycle and were fed standard mouse chow (Teklad 2916, irradiated). Sex-matched, 6–8 week old mice were used for all experiments and co-housed littermates were used as controls. The resource equation method was used for sample size determination (82 (link), 83 (link)). Experiments were performed using protocols (APN 2017–102122) approved by the Institutional Animal Care and Use Committees of the UT Southwestern Medical Center.
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5

Diverse Murine Strains in Immunology

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C57BL/6J (wild-type, Strain #: 000664), B6.SJL-Ptprca PepCb/BoyJ (CD45.1, Strain #: 002014), C57BL/6-Tg(TcraTcrb)1100Mjb/J (OT-I, Strain #: 003831), B6.Cg-Tg(TcraTcrb)425Cbn/J (OT-II, Strain #: 004194), B6(Cg)-Rag2tm1.1Cgn/J (Rag2−/−, Strain #: 008449), B6.129P2(C)Ccr7tm1Rfor/J (Ccr7−/−, Strain #: 006621), B6.129S2-H2dlAb1-Ea/J (MHCII−/−, Strain #: 003584), B6.129P2-B2mtm1Unc/DcrJ (B2m−/−, Strain #: 002087), and C57BL/6-Tg(Nr4a1-EGFP/cre)820Khog/J (Nr4a1GFP, Strain #: 016617) were purchased from the Jackson Laboratory. Ccr4−/ (Chvatchko et al., 2000 (link)), pCX-EGFP (Wright et al., 2001 (link)), and Rag2p-GFP (Boursalian et al., 2004 (link)) strains were generously provided by A.D. Luster (Massachusetts General Hospital, Boston, MA), Irving L. Weissman (Stanford University, Stanford, CA), and Ellen R. Richie (the University of Texas MD Anderson Center, Houston, TX), respectively. Ccr4−/−; Ccr7−/− (DKO), OT-I Rag2−/−, and OT-II Rag2−/− MHCII−/− strains were bred in house. Experiments were performed using mice 4–8 weeks old, except for for autoimmune/inflammatory studies which were carried out in older mice, as specified. All strains were bred and maintained under specific pathogen-free conditions at the Animal Resources Center, the University of Texas at Austin, with procedure approval from the Institutional Animal Care and Use Committee, the University of Texas at Austin.
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6

Genetically Engineered Mouse Models

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All mice used in this study were derived from a C57BL/6 background. B6.129P2(C)-Ccr7tm1Rfor/J, B6.129S2-H2dlAb1-Ea/J, Il17atm1.1(icre)Stck/J, B6.129S7-Rag1tm1Mom/J, B6.129S2(C)-Stat6tm1Gru/J, and B6.129S2-Tcratm1Mom/J mice were purchased from Jackson Laboratories (Bar Harbor, ME). C57BL/6-flt3Ltm1Imx and B10;B6-Rag2tm1Fwa II2rgtm1Wjl mice were purchased from Taconic (Germantown, NY). Mice were housed in specific pathogen–free conditions and were fed ad labitum.
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7

CCR7 and RAG1 knockout mouse protocol

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CCR7−/− (B6.129P2(C)-Ccr7tm1Rfor/J, Stock No. 006621) and RAG1−/− (B6.129S7-Rag1tm1Mom/J, Stock No. 003729) mice on the C57BL/6 background were purchased from Jackson Laboratory and backcrossed onto the 129/SvEv background for more than 6 generations. CCR7 or RAG1 heterozygotes were intercrossed to breed global knockout and wild-type littermates. Male mice between 8–12 weeks old were employed for these experiments. Data, methods, and materials will be made available upon request per TOP Guidelines. All animal procedures were approved by the Durham Veterans’ Affairs Medical Center Institutional Animal Care and Use Committee, and the mice were housed and cared for in accordance with the National Institutes of Health Guide for the Care and Use of Laboratory Animals.
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8

Transgenic Mice for Immune Studies

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FcγRIIb-deficient mice on a C57BL/6 background18 (link) were kindly provided by Jeff Ravetch (Rockefeller University, New York) and Silvia Bolland (National Institutes of Health, NIAID, Bethesda, MD) and crossed to transgenic mice expressing EGFP under the control of the human ubiquitin C promoter38 (Jackson Laboratories) or transgenic mice expressing Venus EYFP under the control of the CD11c promoter39 (obtained from M. Nussenzweig, Rockefeller University, New York, NY). C57BL/6 mice were obtained from Jackson Laboratories or from Charles River Laboratories (Margate, UK). NZB/W F1 were bred in-house from NZB and NZW mice obtained from Harlan UK. CCR7-deficient mice on a C57BL/6 background (strain B6.129P2(C)-Ccr7tm1Rfor/J, stock number 006621, live repository, aged 8 weeks old) were purchased from Jackson Laboratories. Age matched C57BL/6 JAX mice were used as controls. In all experiments, both male and female mice were used. Mice were maintained in specific-pathogen-free conditions at an Association for Assessment and Accreditation of Laboratory Animal Care-accredited animal facility at NIAID or at a Home Office-approved facility in the UK. All procedures were approved by the NIAID Animal Care and Use Committee (National Institutes of Health, Bethesda, MD) or were conducted in accordance with the United Kingdom Animals (Scientific Procedures) Act 1986.
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9

Murine Immune Cell Research Protocol

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C57BL/6 Ly5.1 (CD45.1) and Ly5.2 (CD45.2), WT mice were purchased from Charles River/NCI or Jackson Laboratory. B6.129P2-Ccl5tm1Hso/J, B6.129P2-Ccr5tm1Kuz/J, B6.129S4-Ccr2tm1Ifc/J, B6.129S(C)-Batf3tm1Kmm/J, B6.129P2(C)-Ccr7tm1Rfor/J, B6.129S6-Il10tm1Flv/J, OTI, and OTII were purchased from Jackson Laboratory. All mice were genotyped or phenotyped prior to studies and used at 6–12 wk of age, housed in a specific pathogen–free environment at Dartmouth Hitchcock Medical College, an Association for Assessment and Accreditation of Laboratory Animal Care–accredited institution, and used in accordance with protocols approved by the Institutional Animal Care and Utilization Committee. Both genders were used with no gender-specific effects noticed.
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10

Experimental Mice for Immunological Research

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C57BL/6 and CCR7-deficient mice (B6.129P2(C)-Ccr7tm1Rfor/J) mice were purchased from The Jackson Laboratory (Bar Harbor, ME). All mice used for experiments were 8–16 weeks old, unless specifically noted. Mice were maintained under SPF conditions and all mouse experiments were performed in accordance with University of California Davis Research Animal Resource guidelines.
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