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female wild type fvb n mice  (Charles River Laboratories)

 
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    Charles River Laboratories female wild type fvb n mice
    Female Wild Type Fvb N Mice, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/female+wild+type+fvb+n+mice/fvb+mice/10__26599_slash_nr__2025__94908285-84-1-8
    Average 86 stars, based on 1 article reviews
    female wild type fvb n mice - by Bioz Stars, 2026-09
    86/100 stars

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    Article Title: Gallic acid/copper ion-based metal-phenolic networks as photothermal-enhanced nanocatalysts for cancer therapy
    Article Snippet: Six-week-old female wild-type FVB/N mice were obtained from Charles River (Beijing, China).



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    female wild type fvb n mice  (Charles River Laboratories)
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    Charles River Laboratories female wild type fvb n mice
    Female Wild Type Fvb N Mice, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    female wild type wt fvb n mice  (Charles River Laboratories)
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    wild-type female fvb/n mice  (Charles River Laboratories)
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    Charles River Laboratories wild-type female fvb/n mice
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    wild-type (wt) female fvb/n mice  (Charles River Laboratories)
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    wild type female fvb n mice  (Charles River Laboratories)
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    Charles River Laboratories wild type female fvb n mice
    (A) Schematic of the PCLS generation process. (Diagram created with Biorender.com .) (B) H&E of frozen <t>wild</t> <t>type</t> mouse PCLS at day 1 and day 7 after treatment with Iloprost (3.6μg/ml), vehicle, or empty control. (C) A Presto Blue assay measured viability of wild type mouse PCLS at day 1, 3, and 7 during treatment with vehicle, iloprost (3.6μg/ml), or empty (n=5). Data is shown relative to day 1 (dotted line). (D) PPARγ signaling was measured by PPRE luciferase assay in culture media from PCLS with vehicle or iloprost (3.6ug/ml) at day 6. Data is shown relative to WT control and the assay was conducted in triplicate (n=3). (E) E-cadherin expression in tissue from WT <t>or</t> <t>Fzd9</t> −/− mice with control or iloprost (3.6μg/ml) was measured by qPCR. Assays were conducted in triplicate, data is normalized to RPS18 and shown relative to WT control (n=3). WT, wild type; Fzd9 −/− . Frizzled 9 knockout; ILO, iloprost. Error bars are SEM. Significance was measured by one-way ANOVA with Tukey post-hoc analysis. *p≤0.05
    Wild Type Female Fvb N Mice, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    female wild-type (wt) fvb/n mice  (Charles River Laboratories)
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    Charles River Laboratories female wild-type (wt) fvb/n mice
    (A) Schematic of the PCLS generation process. (Diagram created with Biorender.com .) (B) H&E of frozen <t>wild</t> <t>type</t> mouse PCLS at day 1 and day 7 after treatment with Iloprost (3.6μg/ml), vehicle, or empty control. (C) A Presto Blue assay measured viability of wild type mouse PCLS at day 1, 3, and 7 during treatment with vehicle, iloprost (3.6μg/ml), or empty (n=5). Data is shown relative to day 1 (dotted line). (D) PPARγ signaling was measured by PPRE luciferase assay in culture media from PCLS with vehicle or iloprost (3.6ug/ml) at day 6. Data is shown relative to WT control and the assay was conducted in triplicate (n=3). (E) E-cadherin expression in tissue from WT <t>or</t> <t>Fzd9</t> −/− mice with control or iloprost (3.6μg/ml) was measured by qPCR. Assays were conducted in triplicate, data is normalized to RPS18 and shown relative to WT control (n=3). WT, wild type; Fzd9 −/− . Frizzled 9 knockout; ILO, iloprost. Error bars are SEM. Significance was measured by one-way ANOVA with Tukey post-hoc analysis. *p≤0.05
    Female Wild Type (Wt) Fvb/N Mice, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    female wild-type fvb/n mice  (Charles River Laboratories)
    90
    Charles River Laboratories female wild-type fvb/n mice
    (A) Schematic of the PCLS generation process. (Diagram created with Biorender.com .) (B) H&E of frozen <t>wild</t> <t>type</t> mouse PCLS at day 1 and day 7 after treatment with Iloprost (3.6μg/ml), vehicle, or empty control. (C) A Presto Blue assay measured viability of wild type mouse PCLS at day 1, 3, and 7 during treatment with vehicle, iloprost (3.6μg/ml), or empty (n=5). Data is shown relative to day 1 (dotted line). (D) PPARγ signaling was measured by PPRE luciferase assay in culture media from PCLS with vehicle or iloprost (3.6ug/ml) at day 6. Data is shown relative to WT control and the assay was conducted in triplicate (n=3). (E) E-cadherin expression in tissue from WT <t>or</t> <t>Fzd9</t> −/− mice with control or iloprost (3.6μg/ml) was measured by qPCR. Assays were conducted in triplicate, data is normalized to RPS18 and shown relative to WT control (n=3). WT, wild type; Fzd9 −/− . Frizzled 9 knockout; ILO, iloprost. Error bars are SEM. Significance was measured by one-way ANOVA with Tukey post-hoc analysis. *p≤0.05
    Female Wild Type Fvb/N Mice, supplied by Charles River Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/female+wild+type+fvb+n+mice/c57bl+6+mice/pmc08501067-226-0-7
    Average 90 stars, based on 1 article reviews
    female wild-type fvb/n mice - by Bioz Stars, 2026-09
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    wild type fvb n female mice  (Jackson Laboratory)
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    Jackson Laboratory wild type fvb n female mice
    (A) Schematic of the PCLS generation process. (Diagram created with Biorender.com .) (B) H&E of frozen <t>wild</t> <t>type</t> mouse PCLS at day 1 and day 7 after treatment with Iloprost (3.6μg/ml), vehicle, or empty control. (C) A Presto Blue assay measured viability of wild type mouse PCLS at day 1, 3, and 7 during treatment with vehicle, iloprost (3.6μg/ml), or empty (n=5). Data is shown relative to day 1 (dotted line). (D) PPARγ signaling was measured by PPRE luciferase assay in culture media from PCLS with vehicle or iloprost (3.6ug/ml) at day 6. Data is shown relative to WT control and the assay was conducted in triplicate (n=3). (E) E-cadherin expression in tissue from WT <t>or</t> <t>Fzd9</t> −/− mice with control or iloprost (3.6μg/ml) was measured by qPCR. Assays were conducted in triplicate, data is normalized to RPS18 and shown relative to WT control (n=3). WT, wild type; Fzd9 −/− . Frizzled 9 knockout; ILO, iloprost. Error bars are SEM. Significance was measured by one-way ANOVA with Tukey post-hoc analysis. *p≤0.05
    Wild Type Fvb N Female Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    (A) Schematic of the PCLS generation process. (Diagram created with Biorender.com .) (B) H&E of frozen wild type mouse PCLS at day 1 and day 7 after treatment with Iloprost (3.6μg/ml), vehicle, or empty control. (C) A Presto Blue assay measured viability of wild type mouse PCLS at day 1, 3, and 7 during treatment with vehicle, iloprost (3.6μg/ml), or empty (n=5). Data is shown relative to day 1 (dotted line). (D) PPARγ signaling was measured by PPRE luciferase assay in culture media from PCLS with vehicle or iloprost (3.6ug/ml) at day 6. Data is shown relative to WT control and the assay was conducted in triplicate (n=3). (E) E-cadherin expression in tissue from WT or Fzd9 −/− mice with control or iloprost (3.6μg/ml) was measured by qPCR. Assays were conducted in triplicate, data is normalized to RPS18 and shown relative to WT control (n=3). WT, wild type; Fzd9 −/− . Frizzled 9 knockout; ILO, iloprost. Error bars are SEM. Significance was measured by one-way ANOVA with Tukey post-hoc analysis. *p≤0.05

    Journal: Cancer prevention research (Philadelphia, Pa.)

    Article Title: Precision cut lung slices as a preclinical model for non-small cell lung cancer chemoprevention

    doi: 10.1158/1940-6207.CAPR-23-0004

    Figure Lengend Snippet: (A) Schematic of the PCLS generation process. (Diagram created with Biorender.com .) (B) H&E of frozen wild type mouse PCLS at day 1 and day 7 after treatment with Iloprost (3.6μg/ml), vehicle, or empty control. (C) A Presto Blue assay measured viability of wild type mouse PCLS at day 1, 3, and 7 during treatment with vehicle, iloprost (3.6μg/ml), or empty (n=5). Data is shown relative to day 1 (dotted line). (D) PPARγ signaling was measured by PPRE luciferase assay in culture media from PCLS with vehicle or iloprost (3.6ug/ml) at day 6. Data is shown relative to WT control and the assay was conducted in triplicate (n=3). (E) E-cadherin expression in tissue from WT or Fzd9 −/− mice with control or iloprost (3.6μg/ml) was measured by qPCR. Assays were conducted in triplicate, data is normalized to RPS18 and shown relative to WT control (n=3). WT, wild type; Fzd9 −/− . Frizzled 9 knockout; ILO, iloprost. Error bars are SEM. Significance was measured by one-way ANOVA with Tukey post-hoc analysis. *p≤0.05

    Article Snippet: Animals and PCLS: Frizzled 9 knockout mice ( Fzd9 −/− ) on an FVB/N (RRID:MGI:3528175) background were developed by the Regional Mouse Genetics Core Facility at National Jewish Health and the University of Colorado as previously described. ( 19 ) Wild type female FVB/N mice (eight weeks old, Charles River Laboratories) and female Fzd9 −/− mice were housed in a pathogen-free facility in the Rocky Mountain Regional Veterans Medical Center (RMRVAMC) Veterinary Medical Unit (VMU).

    Techniques: Control, Luciferase, Expressing, Knock-Out

    (A) WT and Fzd9 −/− PCLS were treated with LPS (10ng/ml) for 48 hours and response was measured by qPCR. (B-C) WT and Fzd9 −/− PCLS were treated with iloprost (10μM) or vehicle for 7 days and expression of inflammatory markers (B) and macrophage markers (C) was measured by qPCR. All PCR assays were conducted in triplicate, data is normalized to RPS18 and relative to WT Vehicle. (n=3) (D) WT and Fzd9−/− PCLS were treated with iloprost (3.6ug/ml) or vehicle for 7 days. Protein expression was quantified by dot blot. Data is fold change relative to WT Vehicle. (Blot images in Supplementary Figure S1 , n=1). Significance was measured by one-way ANOVA with Tukey’s post-hoc analysis. *pδ0.05. WT, wild type; ILO, iloprost. Fzd9 −/− , Frizzled 9 knockout.

    Journal: Cancer prevention research (Philadelphia, Pa.)

    Article Title: Precision cut lung slices as a preclinical model for non-small cell lung cancer chemoprevention

    doi: 10.1158/1940-6207.CAPR-23-0004

    Figure Lengend Snippet: (A) WT and Fzd9 −/− PCLS were treated with LPS (10ng/ml) for 48 hours and response was measured by qPCR. (B-C) WT and Fzd9 −/− PCLS were treated with iloprost (10μM) or vehicle for 7 days and expression of inflammatory markers (B) and macrophage markers (C) was measured by qPCR. All PCR assays were conducted in triplicate, data is normalized to RPS18 and relative to WT Vehicle. (n=3) (D) WT and Fzd9−/− PCLS were treated with iloprost (3.6ug/ml) or vehicle for 7 days. Protein expression was quantified by dot blot. Data is fold change relative to WT Vehicle. (Blot images in Supplementary Figure S1 , n=1). Significance was measured by one-way ANOVA with Tukey’s post-hoc analysis. *pδ0.05. WT, wild type; ILO, iloprost. Fzd9 −/− , Frizzled 9 knockout.

    Article Snippet: Animals and PCLS: Frizzled 9 knockout mice ( Fzd9 −/− ) on an FVB/N (RRID:MGI:3528175) background were developed by the Regional Mouse Genetics Core Facility at National Jewish Health and the University of Colorado as previously described. ( 19 ) Wild type female FVB/N mice (eight weeks old, Charles River Laboratories) and female Fzd9 −/− mice were housed in a pathogen-free facility in the Rocky Mountain Regional Veterans Medical Center (RMRVAMC) Veterinary Medical Unit (VMU).

    Techniques: Expressing, Dot Blot, Knock-Out

    Cell types were characterized by Vectra Polaris assay. (A) Percent of total cells labeled as CD45+, T cells, macrophages, and B cells for each mouse group. (B) Normalized cell density of T cells, macrophages, and B cells. (C) Percent of cell types among CD45+ cells from each mouse group. (n=1) WT, wild type; Fzd9 −/− , Fzd9 knockout; ILO, iloprost.

    Journal: Cancer prevention research (Philadelphia, Pa.)

    Article Title: Precision cut lung slices as a preclinical model for non-small cell lung cancer chemoprevention

    doi: 10.1158/1940-6207.CAPR-23-0004

    Figure Lengend Snippet: Cell types were characterized by Vectra Polaris assay. (A) Percent of total cells labeled as CD45+, T cells, macrophages, and B cells for each mouse group. (B) Normalized cell density of T cells, macrophages, and B cells. (C) Percent of cell types among CD45+ cells from each mouse group. (n=1) WT, wild type; Fzd9 −/− , Fzd9 knockout; ILO, iloprost.

    Article Snippet: Animals and PCLS: Frizzled 9 knockout mice ( Fzd9 −/− ) on an FVB/N (RRID:MGI:3528175) background were developed by the Regional Mouse Genetics Core Facility at National Jewish Health and the University of Colorado as previously described. ( 19 ) Wild type female FVB/N mice (eight weeks old, Charles River Laboratories) and female Fzd9 −/− mice were housed in a pathogen-free facility in the Rocky Mountain Regional Veterans Medical Center (RMRVAMC) Veterinary Medical Unit (VMU).

    Techniques: Labeling, Knock-Out