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primary human uterine smooth muscle strain hutsmc  (ATCC)


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    ATCC primary human uterine smooth muscle strain hutsmc
    Primary Human Uterine Smooth Muscle Strain Hutsmc, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 28 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary human uterine smooth muscle strain hutsmc/product/ATCC
    Average 94 stars, based on 28 article reviews
    primary human uterine smooth muscle strain hutsmc - by Bioz Stars, 2026-06
    94/100 stars

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    Inhibitory effect of PDR97 on NF-κB activation in <t>HUtSMCs.</t> (A) NF-κB luciferase activity. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 16 h. (B) Translocation of NF-κB from the cytoplasm to the nucleus. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (C) Analysis of NF-κB protein levels in the cytoplasmic and nuclear fractions. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (D) Quantification of NF-κB protein levels. The relative expression level of NF-κB protein was normalized to the PGF2α- and IL-1β-treated control group. Data are presented as mean ± SEM. Statistical analysis was performed using one-way ANOVA, followed by a nonparametric test. ⁣ ∗ p < 0.05, ⁣ ∗∗ p < 0.01, ⁣ ∗∗∗ p < 0.001, ⁣ ∗∗∗∗ p < 0.0001.
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    Inhibitory effect of PDR97 on NF-κB activation in <t>HUtSMCs.</t> (A) NF-κB luciferase activity. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 16 h. (B) Translocation of NF-κB from the cytoplasm to the nucleus. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (C) Analysis of NF-κB protein levels in the cytoplasmic and nuclear fractions. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (D) Quantification of NF-κB protein levels. The relative expression level of NF-κB protein was normalized to the PGF2α- and IL-1β-treated control group. Data are presented as mean ± SEM. Statistical analysis was performed using one-way ANOVA, followed by a nonparametric test. ⁣ ∗ p < 0.05, ⁣ ∗∗ p < 0.01, ⁣ ∗∗∗ p < 0.001, ⁣ ∗∗∗∗ p < 0.0001.
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    ATCC primary human uterine smooth muscle cells hutsmc
    Inhibitory effect of PDR97 on NF-κB activation in <t>HUtSMCs.</t> (A) NF-κB luciferase activity. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 16 h. (B) Translocation of NF-κB from the cytoplasm to the nucleus. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (C) Analysis of NF-κB protein levels in the cytoplasmic and nuclear fractions. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (D) Quantification of NF-κB protein levels. The relative expression level of NF-κB protein was normalized to the PGF2α- and IL-1β-treated control group. Data are presented as mean ± SEM. Statistical analysis was performed using one-way ANOVA, followed by a nonparametric test. ⁣ ∗ p < 0.05, ⁣ ∗∗ p < 0.01, ⁣ ∗∗∗ p < 0.001, ⁣ ∗∗∗∗ p < 0.0001.
    Primary Human Uterine Smooth Muscle Cells Hutsmc, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/primary human uterine smooth muscle cells hutsmc/product/ATCC
    Average 94 stars, based on 1 article reviews
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    94/100 stars
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    Inhibitory effect of PDR97 on NF-κB activation in HUtSMCs. (A) NF-κB luciferase activity. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 16 h. (B) Translocation of NF-κB from the cytoplasm to the nucleus. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (C) Analysis of NF-κB protein levels in the cytoplasmic and nuclear fractions. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (D) Quantification of NF-κB protein levels. The relative expression level of NF-κB protein was normalized to the PGF2α- and IL-1β-treated control group. Data are presented as mean ± SEM. Statistical analysis was performed using one-way ANOVA, followed by a nonparametric test. ⁣ ∗ p < 0.05, ⁣ ∗∗ p < 0.01, ⁣ ∗∗∗ p < 0.001, ⁣ ∗∗∗∗ p < 0.0001.

    Journal: Mediators of Inflammation

    Article Title: Aster spathulifolius Maxim. Alleviates Primary Dysmenorrhea in a Mouse Model by Modulating Myometrial Contractions via NF-κB/COX-2 Pathway Inhibition

    doi: 10.1155/mi/1654087

    Figure Lengend Snippet: Inhibitory effect of PDR97 on NF-κB activation in HUtSMCs. (A) NF-κB luciferase activity. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 16 h. (B) Translocation of NF-κB from the cytoplasm to the nucleus. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (C) Analysis of NF-κB protein levels in the cytoplasmic and nuclear fractions. HUtSMCs were pretreated with PDR97 for 30 min, followed by coincubation with PGF2α (10 µM) and IL-1β (10 ng/mL) for 30 min. (D) Quantification of NF-κB protein levels. The relative expression level of NF-κB protein was normalized to the PGF2α- and IL-1β-treated control group. Data are presented as mean ± SEM. Statistical analysis was performed using one-way ANOVA, followed by a nonparametric test. ⁣ ∗ p < 0.05, ⁣ ∗∗ p < 0.01, ⁣ ∗∗∗ p < 0.001, ⁣ ∗∗∗∗ p < 0.0001.

    Article Snippet: HUtSMCs were purchased from PromoCell (Cat# C-12575, PromoCell, Heidelberg, Germany).

    Techniques: Activation Assay, Luciferase, Activity Assay, Translocation Assay, Expressing, Control