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B6.129s tnfrsf1atm1imxtnfrsf1btm1imx j

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The B6.129S-Tnfrsf1atm1ImxTnfrsf1btm1Imx/J is a transgenic mouse model that has a targeted mutation in the tumor necrosis factor receptor superfamily, member 1a (Tnfrsf1a) and member 1b (Tnfrsf1b) genes. This model is designed for research purposes.

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6 protocols using b6.129s tnfrsf1atm1imxtnfrsf1btm1imx j

1

Mouse Strains for Immunological Studies

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C57BL/6 wild-type control mice were obtained from the UT Southwestern Mouse Breeding Core Facility. IL-1β−/− mice were generated by David Chaplin, UA at Birmingham and provided to us by Fayyaz S. Sutterwala at Cedars Sinai. Rip3−/− and Rip3−/−Casp8−/− mice were provided by Andrew Oberst at the University of Washington. ASC KO mice were a gift from Genentech. Gsdmd−/− mice were provided by Jonathan Kagan at Boston Children’s Hospital. Caspase-1 KO were provided by Russell Vance at University of California, Berkeley. B6.MRL-Faslpr/J (lpr), B6.129S-Tnftm1Gkl/J (Tnfa−/−), B6.129S-Tnfrsf1atm1ImxTnfrsf1btm1Imx/J (Tnfrsf1a/b−/−), Rag1tm1Mom, Casp1/11null, 2D2 TCR transgenic mice and Zbtb46gfpwere obtained from Jackson Laboratories. All mice were bred and housed in a specific pathogen-free facility at UT Southwestern Medical Center and Cincinnati Children’s Hospital Medical Center. For isolation of steady state CD4 memory T cells, mice were housed in a conventional facility for 2–4 weeks before tissue isolation. All mouse experiments were done as per protocols approved by Institutional Animal Care and Use Committee (IACUC) at UT Southwestern Medical Center and Cincinnati Children’s Hospital Medical Center.
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2

Assessing TNFR1/2 Knockout Mice

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All experiments were carried out in accordance with the Guidelines of the National Institutes of Health (NIH) regarding the care and use of animals for experimental procedures. Protocols were approved by the Institutional Animal Care and Use Committee at the University of Kentucky.
The mice were male WT (B6129SF2/J) and TNFR1/2 KO (B6129S-Tnfrsf1atm1Imx Tnfrsf1btm1Imx/J) (Jackson Laboratory). The mice weighing 20–30 g at the beginning of the study were placed in microisolators and accommodated in ventilated animal housing with a reversed 10/14-h dark/light cycle.
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3

Murine BMDM Preparation Using Knockout Mice

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C57BL/6J (Jackson Laboratories strain #000664), BALB/c (Jackson Laboratories strain #000651), Sting-/- (C57BL/6J-Stinggt/J, Jackson Laboratories strain # 017537), Tlr4-/- (Jackson Laboratories strain #007227) Tlr2-/- (B6.129-tlr2tm1Kir/J, Jackson Laboratories strain #004650), Myd88-/- (B6.129P2(SJL)-Myd88tm1.1Defr/J, Jackson Laboratories strain #009088), TNFAR-/- (B6.129S-Tnfrsf1atm1Imx Tnfrsf1btm1Imx/J, Jackson Laboratories strain #003243), and Trif-/- (C57BL/6J-Ticam1Lps2/J, Jackson Laboratories strain #005037) mice were used for the preparation of BMDM.
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4

Mouse Strains for Immunological Studies

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C57BL/6 wild-type control mice were obtained from the UT Southwestern Mouse Breeding Core Facility. IL-1β−/− mice were generated by David Chaplin, UA at Birmingham and provided to us by Fayyaz S. Sutterwala at Cedars Sinai. Rip3−/− and Rip3−/−Casp8−/− mice were provided by Andrew Oberst at the University of Washington. ASC KO mice were a gift from Genentech. Gsdmd−/− mice were provided by Jonathan Kagan at Boston Children’s Hospital. Caspase-1 KO were provided by Russell Vance at University of California, Berkeley. B6.MRL-Faslpr/J (lpr), B6.129S-Tnftm1Gkl/J (Tnfa−/−), B6.129S-Tnfrsf1atm1ImxTnfrsf1btm1Imx/J (Tnfrsf1a/b−/−), Rag1tm1Mom, Casp1/11null, 2D2 TCR transgenic mice and Zbtb46gfpwere obtained from Jackson Laboratories. All mice were bred and housed in a specific pathogen-free facility at UT Southwestern Medical Center and Cincinnati Children’s Hospital Medical Center. For isolation of steady state CD4 memory T cells, mice were housed in a conventional facility for 2–4 weeks before tissue isolation. All mouse experiments were done as per protocols approved by Institutional Animal Care and Use Committee (IACUC) at UT Southwestern Medical Center and Cincinnati Children’s Hospital Medical Center.
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5

Mouse Strains for Immunology Research

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Six- to 8-week-old C57BL/6 (B6), B6.SJL-Ptprca Pepcb/BoyJ (CD45.1), B6.129S-Tnfrsf1atm1Imx Tnfrsf1btm1Imx/J (TNFR I & II KO), B6.129P2-Cd40tm1Kik/J (CD40 KO), C57BL/6-Prf1tm1Sdz/J (Perforin KO), B6.MRL-Faslpr/J (Fas KO), and B6.129S6-Tbx21tm1Glm/J (T-bet KO) were purchased from the Jackson Laboratory or the National Cancer Institute Mouse Repository (Frederick, MD, USA). B6 IFN-ɣR1-deficient mice were a gift from M. Farrar (University of Minnesota). B6 Cd4-Cre Eomesfl/fl and B6 EomesGFP mice were a gift from S. L. Reiner (Columbia University). B6 DR5 (TRAIL-R KO) deficient mice were a gift from T. S. Griffith (University of Minnesota). Rag1−/− B3K508 TCR transgenic mice (27 (link)) and Rag1−/− SM1 Tbx21ZsGreen TCR transgenic mice were bred and housed in specific pathogen–free conditions in accordance with guidelines of the University of Minnesota Institutional Animal Care and Use Committee and National Institutes of Health. The Institutional Animal Care and Use Committee of the University of Minnesota approved all animal experiments.
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6

Diverse Mouse Models for Immuno-Oncology Research

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C57BL6/J (Jackson 000664), BALB/cJ (Jackson 000651), MMTV-PyMT (FVB/N-Tg(MMTV-PyVT)634Mul/J, Jackson 002374), Rag2−/− (B6(Cg)-Rag2tm1.1Cgn/J, Jackson 008449), TNFR KO (B6.129S-Tnfrsf1atm1ImxTnfrsf1btm1Imx/J, Jackson 003243), C3−/− (B6.129S4-C3tm1Crr/J, Jackson 029661), and Ncf1−/− (B6N.129S2-Ncf1tm1Shl/J, Jackson 027331) mice were purchased from Jackson Laboratory. Fcer1g−/− mice (B6.129P2-Fcer1gtm1Rav N12, Taconic 583) were purchased from Taconic. Rag2−/−Il2rg−/− mice were generated by crossing B6(Cg)-Rag2tm1.1Cgn/J mice (Jackson 008449) with B6.129S4-Il2rgtm1Wjl/J mice (Jackson 003174). Cfp−/− mice67 (link),74 (link) and C6−/− mice75 (link) were generated as previously described. 8–12 week old female mice were used, and mice of different experimental groups and genotypes were cohoused during all experiments, with the exception of immunocompromised Rag2−/− mice. Mice were randomly assigned to experimental groups. All animal studies were performed in accordance with the Stanford University Institutional Animal Care and Use Committee under protocol APLAC-17466. All mice were housed in an American Association for the Accreditation of Laboratory Animal Care-accredited animal facility and maintained in specific pathogen-free conditions.
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