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K18 ace2 2prlmn j

Manufactured by Jackson ImmunoResearch
Sourced in United States, Montenegro

K18-ACE2)2Prlmn/J is a mouse strain that expresses the human ACE2 gene under the control of the cytokeratin 18 (K18) promoter. The core function of this mouse model is to serve as a research tool for studying SARS-CoV-2 infection and associated pathologies.

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5 protocols using k18 ace2 2prlmn j

1

SARS-CoV-2 Infection in Transgenic Mice

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Heterozygous K18-hACE2 C57BL/6J 8-week old male mice (strain: 2B6.Cg-Tg(K18-ACE2)2Prlmn/J, Jackson Laboratory), received 8.4 × 105 TCID50 of SARS-CoV-2/USA/WA1/2020 intranasally, after induction of anesthesia with ketamine hydrochloride and xylazine (PMID: 35304580). Six days after infection, the animals were sacrificed with isofluorane overdose. The tissues were harvested and fixed in 10% formalin for 48 hours.
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2

Evaluation of Monoclonal Antibody Efficacy in K18-hACE2 Mice

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Animal studies were carried out in accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocols were approved by the Institutional Animal Care and Use Committee at the Washington University School of Medicine (assurance number A3381–01). Virus inoculations were performed under anesthesia that was induced and maintained with ketamine hydrochloride and xylazine, and all efforts were made to minimize animal suffering.
Heterozygous K18-hACE2 C57BL/6J mice (strain: 2B6.Cg-Tg(K18-ACE2)2Prlmn/J, Cat # 34860) were obtained from The Jackson Laboratory. Animals were housed in groups and fed standard chow diets.
Eight-week-old female K18-hACE2 C57BL/6 mice were administered 100 μg of 2130-1-0114-112, parental 2130, or isotype control anti-West Nile virus hE16 mAb61 (link) by intraperitoneal injection one day before intranasal inoculation with 104 focus-forming units (FFU) of WA1/2020 D614G, BA.1.1 or BA.5. Animals were euthanized at 4 days post-infection and tissues were harvested for virological analysis.
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3

Animal Housing and Procedures for COVID-19 Research

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Animal housing and experimental procedures have been conducted according to the French and European Regulations (Parlement Européen et du Conseil du 22 Septembre 2010. Décret n°2013-118 du 1er Février 2013 relatif à la protection des animaux utilisés à des fins scientifiques) and the National Research Council (U.S.), Institute for Laboratory Animal Research (U.S.), and National Academies Press (U.S.), Eds., Guide for the care of laboratory animals, 8th ed. Washington, D.C: National Academies Press, 2011. The CIPHE BSL3 facility operates under Agreement N° B 13 014 07 delivered by the French authorities. All animal procedures (including surgery, anesthesia and euthanasia as applicable) used in the current study have been submitted to the Institutional Animal Care and Use Committee of CIPHE approved by French authorities (CETEA DSV -APAFIS#26484-2020062213431976 v6). All the CIPHE BSL3 facility operations are oversee by a Biosecurity/Biosafety Officer and accredited by Agence Nationale de Sécurité du Médicament (ANSM). K18-hACE C57BL/6J mice (strain: 2B6.Cg-Tg (K18-ACE2)2Prlmn/J) were obtained from The Jackson Laboratory. Animals were housed in groups and fed standard chow diets.
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4

SARS-CoV-2 Infection of K18-ACE2 Mice

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All animal experiments were conducted under biosafety level 3 confinement and approved by the Université Laval animal committee. Nine-week old female B6.Cg-Tg (K18-ACE2)2Prlmn/J (stock# 3034860) (K18-ACE2 mice) were purchased from the Jackson Laboratories (Bar Harbor, ME). Mice were anesthetized using isoflurane and infected by intranasal delivery of 25 ul of saline containing 4.5x104 TCID50 of SARS-CoV-2. Mock-treated mice received 25 ul of saline. Mouse body temperature and weight were recorded every day for 7 days. On day 1, 2, 3, 4, 5 and 7, mice (n=5/group) were euthanized, and lungs collected for assessment of viral loads, RNA extraction, tissue homogenization for cytokine lipid mediators of inflammation analysis and histological studies.
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5

Murine SARS-CoV-2 Infection Model

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Animal studies were carried out in accordance with the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health. The protocols were approved by the Institutional Animal Care and Use Committee at the Washington University School of Medicine (assurance number A3381–01). Virus inoculations were performed under anesthesia that was induced and maintained with ketamine hydrochloride and xylazine, and all efforts were made to minimize animal suffering. Heterozygous K18-hACE2 C57BL/6J mice (strain: 2B6.Cg-Tg(K18-ACE2)2Prlmn/J, Cat # 34860) and 129S2 mice (strain: 129S2/SvPasCrl, Cat # 287) were obtained from The Jackson Laboratory and Charles River Laboratories, respectively. Animals were housed in groups and fed standard chow diets.
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