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primary human prostatic smooth muscle cells  (Lonza)


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    Structured Review

    Lonza primary human prostatic smooth muscle cells
    Human prostate <t>SMCs</t> (A), ECs (B), and SCs (C) exhibited explicit reactions to hypoxia and oxidative stress. Lipid peroxidation was more prevalent in SMCs, whereas ECs appeared more susceptible to protein oxidation. Hypoxia caused lipid peroxidation in SMCs and protein oxidation in ECs. Oxidative stress led to protein oxidation and lipid peroxidation in SMCs, ECs, and SCs. Protein oxidation and lipid peroxidation suggest damage to protein- and lipid-containing structures of the cells, respectively. SMC, smooth muscle cell; <t>EC,</t> <t>epithelial</t> cell; SC, stromal cell; AOPP, advanced oxidation protein product; MDA, malondialdehyde. * Represent significance versus control.
    Primary Human Prostatic Smooth Muscle Cells, supplied by Lonza, 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/result/primary human prostatic smooth muscle cells/product/Lonza
    Average 90 stars, based on 1 article reviews
    primary human prostatic smooth muscle cells - by Bioz Stars, 2026-02
    90/100 stars

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    1) Product Images from "Structural modifications of the prostate in hypoxia, oxidative stress, and chronic ischemia"

    Article Title: Structural modifications of the prostate in hypoxia, oxidative stress, and chronic ischemia

    Journal: Korean Journal of Urology

    doi: 10.4111/kju.2015.56.3.187

    Human prostate SMCs (A), ECs (B), and SCs (C) exhibited explicit reactions to hypoxia and oxidative stress. Lipid peroxidation was more prevalent in SMCs, whereas ECs appeared more susceptible to protein oxidation. Hypoxia caused lipid peroxidation in SMCs and protein oxidation in ECs. Oxidative stress led to protein oxidation and lipid peroxidation in SMCs, ECs, and SCs. Protein oxidation and lipid peroxidation suggest damage to protein- and lipid-containing structures of the cells, respectively. SMC, smooth muscle cell; EC, epithelial cell; SC, stromal cell; AOPP, advanced oxidation protein product; MDA, malondialdehyde. * Represent significance versus control.
    Figure Legend Snippet: Human prostate SMCs (A), ECs (B), and SCs (C) exhibited explicit reactions to hypoxia and oxidative stress. Lipid peroxidation was more prevalent in SMCs, whereas ECs appeared more susceptible to protein oxidation. Hypoxia caused lipid peroxidation in SMCs and protein oxidation in ECs. Oxidative stress led to protein oxidation and lipid peroxidation in SMCs, ECs, and SCs. Protein oxidation and lipid peroxidation suggest damage to protein- and lipid-containing structures of the cells, respectively. SMC, smooth muscle cell; EC, epithelial cell; SC, stromal cell; AOPP, advanced oxidation protein product; MDA, malondialdehyde. * Represent significance versus control.

    Techniques Used: Control

    Nonconforming oxygen tension led to widespread DNA damage in cultured human prostatic cells. Both hypoxia and oxidative stress induced DNA damage in SMCs (A), ECs (B), and SCs (C), characterized by a significant increase in 8-hydroxy-2'-deoxyguanosine levels. SMC, smooth muscle cell; EC, epithelial cell; SC, stromal cell. * Represent significance versus control.
    Figure Legend Snippet: Nonconforming oxygen tension led to widespread DNA damage in cultured human prostatic cells. Both hypoxia and oxidative stress induced DNA damage in SMCs (A), ECs (B), and SCs (C), characterized by a significant increase in 8-hydroxy-2'-deoxyguanosine levels. SMC, smooth muscle cell; EC, epithelial cell; SC, stromal cell. * Represent significance versus control.

    Techniques Used: Cell Culture, Control



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