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human thyroid follicular epithelial cell line nthy ori  (Procell Inc)

 
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    Procell Inc human thyroid follicular epithelial cell line nthy ori
    Characterizations of the RSL3-MBs (A) Microscopic image of RSL3-MBs. Scale bars, 5 μm. (B) Size distribution of the MBs and RSL3-MBs. (C) Zeta potential of MBs and RSL3-MBs ( n = 3 per group; mean ± SEM; and independent samples t test). (D) Size changes of RSL3-MBs within 1.5 h after preparation. (E) Viability <t>of</t> <t>Nthy-ori</t> 3-1 cells incubated with different concentrations of MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (F) Viability of Nthy-ori 3-1 cells incubated with different concentrations of RSL3-MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (G) HE staining of heart, liver, spleen, lung, and kidney sections at day 12 after injection of MBs and RSL3-MBs. Scale bars, 50 μm.
    Human Thyroid Follicular Epithelial Cell Line Nthy Ori, supplied by Procell Inc, 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/result/human thyroid follicular epithelial cell line nthy ori/product/Procell Inc
    Average 86 stars, based on 1 article reviews
    human thyroid follicular epithelial cell line nthy ori - by Bioz Stars, 2026-05
    86/100 stars

    Images

    1) Product Images from "Ultrasound-targeted microbubble destruction enhances RSL3-induced ferroptosis in anaplastic thyroid carcinoma"

    Article Title: Ultrasound-targeted microbubble destruction enhances RSL3-induced ferroptosis in anaplastic thyroid carcinoma

    Journal: iScience

    doi: 10.1016/j.isci.2026.114993

    Characterizations of the RSL3-MBs (A) Microscopic image of RSL3-MBs. Scale bars, 5 μm. (B) Size distribution of the MBs and RSL3-MBs. (C) Zeta potential of MBs and RSL3-MBs ( n = 3 per group; mean ± SEM; and independent samples t test). (D) Size changes of RSL3-MBs within 1.5 h after preparation. (E) Viability of Nthy-ori 3-1 cells incubated with different concentrations of MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (F) Viability of Nthy-ori 3-1 cells incubated with different concentrations of RSL3-MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (G) HE staining of heart, liver, spleen, lung, and kidney sections at day 12 after injection of MBs and RSL3-MBs. Scale bars, 50 μm.
    Figure Legend Snippet: Characterizations of the RSL3-MBs (A) Microscopic image of RSL3-MBs. Scale bars, 5 μm. (B) Size distribution of the MBs and RSL3-MBs. (C) Zeta potential of MBs and RSL3-MBs ( n = 3 per group; mean ± SEM; and independent samples t test). (D) Size changes of RSL3-MBs within 1.5 h after preparation. (E) Viability of Nthy-ori 3-1 cells incubated with different concentrations of MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (F) Viability of Nthy-ori 3-1 cells incubated with different concentrations of RSL3-MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (G) HE staining of heart, liver, spleen, lung, and kidney sections at day 12 after injection of MBs and RSL3-MBs. Scale bars, 50 μm.

    Techniques Used: Zeta Potential Analyzer, Incubation, Staining, Injection



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    Characterizations of the RSL3-MBs (A) Microscopic image of RSL3-MBs. Scale bars, 5 μm. (B) Size distribution of the MBs and RSL3-MBs. (C) Zeta potential of MBs and RSL3-MBs ( n = 3 per group; mean ± SEM; and independent samples t test). (D) Size changes of RSL3-MBs within 1.5 h after preparation. (E) Viability <t>of</t> <t>Nthy-ori</t> 3-1 cells incubated with different concentrations of MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (F) Viability of Nthy-ori 3-1 cells incubated with different concentrations of RSL3-MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (G) HE staining of heart, liver, spleen, lung, and kidney sections at day 12 after injection of MBs and RSL3-MBs. Scale bars, 50 μm.
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    Characterizations of the RSL3-MBs (A) Microscopic image of RSL3-MBs. Scale bars, 5 μm. (B) Size distribution of the MBs and RSL3-MBs. (C) Zeta potential of MBs and RSL3-MBs ( n = 3 per group; mean ± SEM; and independent samples t test). (D) Size changes of RSL3-MBs within 1.5 h after preparation. (E) Viability <t>of</t> <t>Nthy-ori</t> 3-1 cells incubated with different concentrations of MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (F) Viability of Nthy-ori 3-1 cells incubated with different concentrations of RSL3-MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (G) HE staining of heart, liver, spleen, lung, and kidney sections at day 12 after injection of MBs and RSL3-MBs. Scale bars, 50 μm.
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    Characterizations of the RSL3-MBs (A) Microscopic image of RSL3-MBs. Scale bars, 5 μm. (B) Size distribution of the MBs and RSL3-MBs. (C) Zeta potential of MBs and RSL3-MBs ( n = 3 per group; mean ± SEM; and independent samples t test). (D) Size changes of RSL3-MBs within 1.5 h after preparation. (E) Viability <t>of</t> <t>Nthy-ori</t> 3-1 cells incubated with different concentrations of MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (F) Viability of Nthy-ori 3-1 cells incubated with different concentrations of RSL3-MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (G) HE staining of heart, liver, spleen, lung, and kidney sections at day 12 after injection of MBs and RSL3-MBs. Scale bars, 50 μm.
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    Image Search Results


    Characterizations of the RSL3-MBs (A) Microscopic image of RSL3-MBs. Scale bars, 5 μm. (B) Size distribution of the MBs and RSL3-MBs. (C) Zeta potential of MBs and RSL3-MBs ( n = 3 per group; mean ± SEM; and independent samples t test). (D) Size changes of RSL3-MBs within 1.5 h after preparation. (E) Viability of Nthy-ori 3-1 cells incubated with different concentrations of MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (F) Viability of Nthy-ori 3-1 cells incubated with different concentrations of RSL3-MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (G) HE staining of heart, liver, spleen, lung, and kidney sections at day 12 after injection of MBs and RSL3-MBs. Scale bars, 50 μm.

    Journal: iScience

    Article Title: Ultrasound-targeted microbubble destruction enhances RSL3-induced ferroptosis in anaplastic thyroid carcinoma

    doi: 10.1016/j.isci.2026.114993

    Figure Lengend Snippet: Characterizations of the RSL3-MBs (A) Microscopic image of RSL3-MBs. Scale bars, 5 μm. (B) Size distribution of the MBs and RSL3-MBs. (C) Zeta potential of MBs and RSL3-MBs ( n = 3 per group; mean ± SEM; and independent samples t test). (D) Size changes of RSL3-MBs within 1.5 h after preparation. (E) Viability of Nthy-ori 3-1 cells incubated with different concentrations of MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (F) Viability of Nthy-ori 3-1 cells incubated with different concentrations of RSL3-MBs ( n = 5 per group; mean ± SEM; and one-way ANOVA). (G) HE staining of heart, liver, spleen, lung, and kidney sections at day 12 after injection of MBs and RSL3-MBs. Scale bars, 50 μm.

    Article Snippet: The human thyroid follicular epithelial cell line Nthy-ori 3-1 (CL-0817) and the human anaplastic thyroid cancer cell line CAL-62 (CL-0618) were obtained from Procell Life Science & Technology Co., Ltd.

    Techniques: Zeta Potential Analyzer, Incubation, Staining, Injection

    Fig. 1. PLOD1 expression was positively correlated with THCA progression. A-C. PLOD1 expression in TCGA-THCA database was analyzed by the Ualcan website. D. The overall survival (OS) rates were determined using GEPIA website. E-G. PLOD1 expression in THCA tissues and its paired adjacent normal tissues was assessed via western blot, qRT-PCR and immunohistochemistry assay. H and I. PLOD1 levels in THCA cells (BHT101, KTC1, TPC1 and CAL-62) and the primary human thyroid follicular epithelial cell line (Nthy-ori 3–1) were tested via qRT-PCR and western blot. *P < 0.05.

    Journal: Genomics

    Article Title: PLOD1 promote proliferation and migration with glycolysis via the Wnt/β-catenin pathway in THCA.

    doi: 10.1016/j.ygeno.2024.110943

    Figure Lengend Snippet: Fig. 1. PLOD1 expression was positively correlated with THCA progression. A-C. PLOD1 expression in TCGA-THCA database was analyzed by the Ualcan website. D. The overall survival (OS) rates were determined using GEPIA website. E-G. PLOD1 expression in THCA tissues and its paired adjacent normal tissues was assessed via western blot, qRT-PCR and immunohistochemistry assay. H and I. PLOD1 levels in THCA cells (BHT101, KTC1, TPC1 and CAL-62) and the primary human thyroid follicular epithelial cell line (Nthy-ori 3–1) were tested via qRT-PCR and western blot. *P < 0.05.

    Article Snippet: The primary human thyroid follicular epithelial cell line (Nthy-ori 3–1) was supplied by Procell Life Science&Technology Co.,Ltd. (Wuhan, China).

    Techniques: Expressing, Western Blot, Quantitative RT-PCR, Immunohistochemistry