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Female balb c

Manufactured by Taconic Biosciences
Sourced in United States

The Female BALB/c is a mouse strain commonly used in research. It is an inbred laboratory mouse strain developed by the Bagg Albino mouse colony. The BALB/c strain is widely used in various fields of biomedical research due to its well-characterized genetic and physiological characteristics.

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4 protocols using female balb c

1

Murine Tumor Cell Derivation and Culture

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Female BALB/c and C57BL/6 mice were purchased from Taconic Biosciences, Inc. (Germantown, NY) and housed in specific pathogen-free conditions in the University of Pittsburgh animal facility. All animal studies were approved by the Institutional Animal Care and Use Committee. Murine malignant mesothelioma cell line AB12 was derived from an asbestos-induced BALB/c mouse,49 (link) and it was a gift kindly provided by Dr. Steven M Albelda (University of Pennsylvania). AB12 cells were infected with firefly luciferase-carrying lentivirus and selected by blasticidin to generate a new subline AB12-luc. Murine colon adenocarcinoma cell line CA51 was derived from a tissue collection of the National Cancer Institute. All cell lines were grown in Dulbecco's modified Eagle's medium (DMEM) supplemented with 10% fetal bovine serum (FBS), 2 mM L-glutamine, and 1X penicillin/streptomycin solution (Invitrogen, Carlsbad, CA) in 37°C, 5% CO2 incubator.
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2

Preclinical Evaluation of CNP(MMAE) in HGSOC

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Female BALB/c (non-tumor bearing) mice at 4–6 weeks of age (Taconic, USA) were utilized for toxicity experiments (at MIT). Female NCR nu/nu mice at 5 weeks of age were used for pharmacology and efficacy experiments upon establishment of a disseminated cell-line xenograft model of HGSOC (8 × 105 LUC+/RFP+ OVCAR8 cells/animal; 0.5 mL; IP injection) and were similarly purchased from Taconic. C.B-17/Icr-SCID/Sed mice were purchased from Charles River and bred at MGH; they were implanted with primary cells obtained from a patient with “platinum-resistant” and advanced-stage HGSOC after lentiviral transduction of firefly luciferase, establishing LUC+ PDX tumors (10 million cells/animal; 0.5 mL PBS; IP injection); assessments of CNP(MMAE) pharmacology and efficacy were performed in these PDX models. Tumor growth was monitored by BLI. All animal studies were performed under protocols approved by the MIT CAC (0615-069-1) and by the Massachusetts General Hospital IACUC (2009N000117).
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3

Standardized Mouse Housing Protocols

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Female BALB/c and C57BL/6 mice (6–8 weeks old) were purchased from Taconic Farms. Animals were housed in specific pathogen–free conditions in a vivarium (5 mice per cage), and all experiments were performed under Institutional Animal Care and Use Committee (IACUC) approved protocols and guidelines at Avastus Preclinical Services (Cambridge, MA). Mice were allowed to acclimate in the vivarium for 1–2 weeks prior to the start of experiments. Mice were monitored daily, provided PicoLab Rodent Diet 20 and autoclaved water ad libitum.
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4

Mouse Acclimation and Housing Protocol

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Female BALB/c and C57BL/6 mice (6-8 weeks old) were purchased from Taconic Farms. Animals were housed in specific pathogen–free conditions in a vivarium (5 mice per cage), and all experiments were performed under Institutional Animal Care and Use Committee (IACUC) approved protocols and guidelines at Avastus Preclinical Services (Cambridge, MA). Female SJL mice (8-10 weeks old) were purchased from Jackson Labs for EAE experiments which were performed under IACUC approved protocols at Hooke Laboratories (Lawrence, MA). Mice were allowed to acclimate in the vivarium for 1-2 weeks prior to the start of experiments. PicoLab Rodent Diet 20 was provided and autoclaved water via sipper bottle, given ad libitum and checked daily.
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