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Athymic nude nu j mice

Manufactured by Jackson ImmunoResearch
Sourced in Montenegro

Athymic nude (NU/J) mice are a laboratory mouse strain that lack a functional thymus gland, resulting in a deficiency of T cells. This strain is widely used in biomedical research, particularly in the areas of cancer, immunology, and xenograft studies.

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8 protocols using athymic nude nu j mice

1

Xenograft Lung Tumor Model in Mice

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NU/J athymic nude mice (Strain #:002019 RRID:IMSR_JAX:002019) were requested from Jackson Labs. All animal studies were approved by, and were performed in compliance with Animal Care and Use Committee (IACUC) at University of Texas, MD Anderson Cancer Center. 500,000 cells were suspended in sterile ice-cold PBS (1X) and injected into the tail-vein of mice. Mice were monitored daily for tumor formation, and hyperpnea. Lungs were excised and stored in 10% formalin for analysis.
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2

Xenograft Tumor Growth Assay

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All experiments were conducted in accordance with general guidelines in the protocol approved by the Institutional Animal Care and Use Committee (IACUC) at Meharry Medical College. The facilities and laboratory animals programs at Meharry Medical College are accredited by the Association for the Assessment and Accreditation of Laboratory Animal Care. The IACUC ensured that animal related experiments adhered to the National Institutes of Health (NIH) guidelines for the humane care and use of laboratory animals. The 5 to 6 week old female Nu/J athymic nude mice were obtained from Jackson Laboratories. Suspensions of control, AnxA6 down-regulated and AnxA6 deficient BT-549 cells (1 × 106 viable cells/100 μl)or control and AnxA6 expressing HCC1806 cells (2 × 106 viable cells/100 μl) were subcutaneously injected into the mammary fat pads of the mice (n = 8). Tumor growth was monitored by bi-weekly measurement of tumor volume. Mice were euthanized at the end of the experiment or when tumors were ~2,000 mm3. Tumor tissues were processed for H&E and immunohistochemical staining according to standard procedures.
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3

Mouse Xenograft Tumor Model Protocols

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Female, 8–10 wk old, C57Bl/6 J wild-type (strain #000664), C57Bl/6 J p53KO (#002101), and athymic nude NU/J mice (#002019) were purchased from The Jackson Laboratory. Mice were housed at ambient room temperature (74 ± 2 °F) with humidity of 30–70% and a light/dark cycle of 14 h/10 h. Tumor burden did not exceed 1.5 cm3. Maximal tumor burden and all other aspects of animal experiments were performed in accordance with the guidelines of Cedars-Sinai Medical Center Institutional Animal Care and Use Committee. The human 293 T cells line for viral preparation was purchased from ATCC. 293 T were grown in DMEM, supplemented with glutamine, 10% fetal bovine serum (Gibco), 100 IU/ml penicillin, and 100 μg/ml streptomycin (Gibco). Cells were cultured in an incubator at 37 °C and 5% CO2.
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4

Flavopiridol Inhibits Metastasis in Nude Mice

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Athymic nude (NU/J) mice were obtained from The Jackson Laboratories. 2 × 106 cells (SJSA-1 or 143B) were injected into the tail vein of the mice. For the following 21 days, mice received daily intra-peritoneal injections of saline or 2.5 mg/kg flavopiridol. After 21 days, mice were euthanized and lungs were collected for analysis. Metastatic burden was measured as number of metastatic nodules for the 143B cell line and individual lung weight was used for SJSA-1 due to high number of the metastatic nodules in the control group. The University of California Irvine Institutional Animal Care and Use Committee approved all animal procedures. Three animals were used for each group.
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5

Xenograft Mouse Model for Astrocyte Study

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All animal procedures used in this study were performed in accordance with protocols approved by the Institutional Animal Care and Use Committee of the University of Pennsylvania. Animals were housed at a maximum of five per cage with a 14-hr light/10-hr dark cycle with food and water ad libitum. Female 4–8-week-old athymic nude (NU/J) mice (The Jackson Laboratory) were used for transplantation experiments. P3 CD-1 mice pups (Charles River) were used for isolation of hypothalamic astrocytes to prepare astrocyte-conditioned medium.
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6

Mouse Models for Preclinical Studies

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All mouse experiments were performed in accordance with, and with the approval of Purdue University IACUC. Five to 6-week old female BALB/c and athymic Nude (NU/J) mice were purchased from Jackson Laboratories. Female NRG (NOD-Rag1null IL2rgnull, NOD rag gamma) were purchased from Biological Evaluation Shared Resource facility at Purdue University.
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7

Xenograft Model for Breast Cancer Study

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All procedures performed in studies involving animals were in accordance with the ethical standards of the University of Minnesota and approved by the Institutional Animal Care and Use Committee (IACUC). Four-week-old, male, athymic nude (NU/J) mice (Jackson Laboratory) were anesthetized with isofluorane (induced at 5% and maintained at 2% in 1 mL/min O2) and inoculated with 2.5×106 EpCAMHigh MCF-7 cells on the left shoulder and 2.5×106 EpCAMLow MDA-MB-231 cells on the right shoulder, each as a 50% v/v suspension in Matrigel Matrix (Corning, Cat: 354248). Xenografts were allowed to grow for two weeks, yielding tumors of 8–12 mm in diameter. To support MCF-7 cell growth, the mice’s water supply was supplemented with 500 µM 17-β-estradiol valerate.
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8

Athymic Nude Mice for Preclinical Studies

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Athymic nude NU/J mice from Jackson Laboratories (Bar Harbor, Maine) were used for imaging (n = 8) and pharmacokinetic studies (n = 48). Athymic nude CrTac:NCr-Foxn1nu mice from Taconic Laboratories (Hudson, NY) were used to determine the stability of PARPi-FL (n = 18). They were further used for orthotopic mouse models (n = 24). For in vivo toxicology, B6D2F1 mice from Jackson Laboratories (Bar Harbor, Maine) were used. For subcutaneous injections, mice were anesthetized with 2% isoflurane gas in 2 L/min medical air. For orthotopic injections, mice were anesthetized with a 150 mg/kg ketamine and 15 mg/kg xylazine cocktail (10 μL/g). For all intravenous injections, mice were gently warmed with a heat lamp, placed on a restrainer, tail sterilized with alcohol pads, and the injection was placed into a lateral tail vein. All animal experiments were done in accordance with protocols approved by the Institutional Animal Care and Use Committee of MSKCC and followed National Institutes of Health guidelines for animal welfare.
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