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B6.129 tlr2tm1kir j

Manufactured by Jackson ImmunoResearch
Sourced in United States, Montenegro

B6.129-Tlr2tm1Kir/J is a genetically modified mouse strain that carries a targeted mutation in the Tlr2 gene. The core function of this mouse model is to facilitate the study of Toll-like receptor 2 (TLR2) and its role in various biological processes.

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39 protocols using b6.129 tlr2tm1kir j

1

Rodent Models for Immunology Research

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Female Wistar rats (175–225 g) were obtained from Janvier Labs (Le Genest-Saint Isle), while mice (male C57BL/6J wild type, B6.B10ScN-Tlr4lps-del/JthJ (Tlr4 KO) and B6.129-Tlr2 < tm1Kir >/J (Tlr2 KO)) were obtained from Jackson Laboratory (CA, USA). Animals were maintained at the unit of animal research (Biomedical Research Center, University of Granada, Granada, Spain) in air-conditioned animal quarters with a 12 h light-dark cycle in specific pathogen-free (SPF) conditions, with free access to autoclaved tap water and food (Harlan-Teklad 2014, Harlan Ibérica, Barcelona, Spain). This study was in accordance with Directive 2010/63/EU and approved by the ethical committee (ref. ES 01/03/2017/029, Granada, Spain).
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2

Pathogen-Free Murine Experiment

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Wild-type (WT) C57BL/6 and TLR2 knockout (KO) mice (B6.129-Tlr2tm1Kir/J) were purchased from the Jackson Laboratory (Bar Harbor, ME). Experiments using these animals were approved by the Institutional Animal Care and Use Committee of the Forsyth Institute. All the mice used in the study (4 weeks old, male: female=2:1) were maintained in specific pathogen-free units of the Forsyth Institute Animal Facility. Mice were fed a soft diet ad libitum for the duration of the experiment.
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3

Evaluation of NLY01 in α-synuclein mouse models

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All experimental procedures were according to the guidelines of Laboratory Animal Manual of the National Institute of Health Guide to the Care and Use of Animals, which were approved by the Johns Hopkins Medical Institute Animal Care and Use Committee. The PK studies in cynomolgus monkeys were approved by the Institutional Animal Care and Use Committee of Korea Institute of Toxicology (KIT, study plan JN13002) and performed at KIT, Daejeon, Republic of Korea. (1) Mouse strain for stereotaxic α-syn PFF injection. C57BL6 mice were obtained from the Jackson Laboratories (ME, USA). The mice do not develop any autoimmune or inflammatory phenotype. NLY01 (3 mg/kg) two times per week was subcutaneously administered one month after α-syn PFF stereotaxic injection until five months. (2) hA53T α-synuclein transgenic mice. hA53T α-synuclein transgenic mice were obtained from the Jackson Laboratories (B6; Prnp-SNCA*A53T)16 (link). NLY01 (3 mg/kg) two times per week was subcutaneously administered to six-months-old hA53T α-synuclein transgenic mice until ten-months of age or until death. (3) Toll like receptor 2 (TLR-2) knockout mice. TLR-2 KO mice were obtained from the Jackson Laboratories (B6; 129-Tlr2 tm1kir/J).
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4

TLR2 and TLR4 Double Knockout Mice

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TLR2/4 DKO mice, as well as their wild-type (WT) (C57BL/6 J) mice, were used in this study (6- to 8-week-old). To generate TLR2/4 DKO mice, TLR2 KO mice (B6.129-Tlr2tm1Kir/J; Jackson Laboratory) and TLR4 KO mice (a generous gift from Dr. Shizuo Akira, Osaka University, Osaka, Japan) were intercrossed. Animals were kept in conventional animal housing with a 12-h light-dark cycle at constant temperature. The experimental procedures were approved by the Institutional Animal Care and Use Committee (IACUC) at the Forsyth Institute.
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5

Characterization of Knockout Mouse Models

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Wild type BALB/cJ and C57BL/6J mice along with mutant knockout mice B6.129-Tlr2tm1Kir/J, B6.129S1-Nod2tm1Flv/J, and B6.129S1-Tlr5tm1Flv/J were purchased from The Jackson Laboratory (Bar Harbor, ME, USA). Caspase1-/- on the C57BL/6 background were generously gifted from Dr. J. P. Ting (UNC-Chapel Hill) [18 (link)]. Nod2-/- mice on the BALB/c background were generously provided by Dr. Holly Rosenzweig (Oregon Health & Science University), bred at CSU, and Nod2-/- genotype was confirmed [19 (link)].
All animals were age matched (8–12 weeks), maintained in specific pathogen free conditions, individually tracked and monitored daily for clinical signs of stress or illness, including but not limited to changes in skin and hair, eyes and mucous membranes, respiratory system, circulatory system, central nervous system, salivation, diarrhea, or lethargy. Upon arrival, animals were housed socially (2–5) in commercially available, individually ventilated caging systems with a 12 h light/12 h dark cycle. Animals were provided ad libitum commercial irradiated rodent chow (Teklad Global) and tap water filtered via reverse osmosis in autoclaved water bottles; all bedding and enrichment materials was autoclaved prior to use and changed regularly.
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6

Bone Marrow-Derived Macrophage Isolation

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All animal use protocols were approved by the MGH IACUC and carried out in accordance with national guidelines for the ethical use of animals in research. C57BL/6J (Jackson Laboratories strain [Bar Harbor, ME, USA] Number 000664), Tlr2−/− (B6.129-tlr2tm1Kir/J, Jackson Laboratories strain number 004650), Sting−/− (C57BL/6J-Stinggt/J, Jackson Laboratories strain number 017537), and cGAS−/− (B6(C)-Cgastm1d(EUCOMM)Hmgu/J, Jackson Laboratories strain number 026554) mice were ordered from Jackson Laboratories. Mice were euthanized by carbon-dioxide inhalation, and femurs and tibias were harvested for bone marrow isolation. Bone marrow cells were incubated at 37°C with 5% carbon dioxide in BMDM media (DMEM [Gibco, Billings, Montana, USA] with 20% fetal bovine serum [Hyclone, Logan, Utah, USA] and 25 ng/mL recombinant mouse M-CSF [R and D Systems, Minneapolis, MN, USA]) on petri dishes. After 6 days, adherent cells were washed and harvested for use as bone marrow-derived macrophages.
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7

Murine Model for Immunological Studies

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C57Bl/6J (B6) and B6.SJL-PtprcaPepcb/BoyJ (B6-CD45.1), and B6.129-Tlr2tm1Kir/J (TLR2 KO) mice were obtained from The Jackson Laboratory (Bar Harbor, ME, USA). TLR2 KO mice were bred in-house and were age-matched with vendor-purchased B6 mice. Female B6 and TLR2 KO mice were between 6 and 10 weeks old at the time of inoculation. All mice were housed in specific pathogen-free conditions at the University of Arizona in accordance with the Institutional Animal Care and Use Committee (IACUC).
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8

Murine Model for Tuberculosis Research

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Female, specific pathogen-free (SPF), 6–7-week-old C57BL/6J (H-2Kb and I-Ab), BALB/c (H-2Kd and I-Ad) mice were purchased from Japan SLC, Inc. (Shizuoka, Japan). Age- and gender-matched ovalbumin (OVA)-specific T cell receptor (TCR) transgenic mice, TLR2 knockout (K/O) mice (B6.129-Tlr2tm1Kir/J), and TLR4 K/O mice (C57BL/10ScNJ) in a C57BL/6J background were purchased from the Jackson Laboratory (Bar Harbor, ME). The animals were fed a sterile commercial mouse diet and provided with water ad libitum. Mice infected with Mtb H37Rv were housed under adequate conditions in a BL-3 biohazard animal barrier facility at the Avison Biomedical Research Center, Yonsei College of Medicine. The animal experiments complied with the Ethics Committee and Institutional Animal Care and Use Committee of Yonsei University Health System (Permission no.: 2016-019).
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9

Generation and Analysis of Genetically Modified Mice

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WT C57BL/6J (JAX:000664), CD45.1 (B6.SJL-Ptprca Pepcb/BoyJ, JAX:02014), TLR2–/– (B6.129-Tlr2tm1Kir/J, JAX:004650), TLR4–/– (B6.B10ScN-Tlr4lps–del/JthJ, JAX:007227), Rag2–/– (B6(Cg)-Rag2tm.1Cgn/J, JAX:008449), and OTII (B6.Cg-Tg[TcraTcrb]425Cbn/J, JAX:004194) mice were purchased from The Jackson Laboratory. Tlr2–/– Tlr4–/– mice were generated by crossing TLR2–/– and TLR4–/– mice. Batf3–/– (C.129S-Batf3tm1Kmm/J, JAX:013756) mice were obtained via Miriam Merad (Precision Immunology Institute and Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA).
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10

Isolation and Infection of Mouse BMMs

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WT (C57BL/6J), TLR2−/− (B6.129-Tlr2tm1Kir/J), MYD88−/− (B6.129P2(SJL)-Myd88tm1.1Defr/J), and p47phox−/− (B6N.129S2-Ncf1tm1Shl/J) mice were purchased from The Jackson Laboratory. Female mice were 6–8 weeks old and were used for isolation of BMMs and mouse infections.
All protocols involving animals were approved by the Institutional Animal Care and Use Committee of Stony Brook University.
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