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p enos ser1177  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc p enos ser1177
    P Enos Ser1177, supplied by Cell Signaling Technology 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/product/p+enos/pmc12964221-5-0-3
    Average 86 stars, based on 1 article reviews
    p enos ser1177 - by Bioz Stars, 2026-11
    86/100 stars

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    Related Articles

    Cell-Signaling:

    Article Title: Polyethylene terephthalate microplastics impair erectile function through macrophage mediated cGAS-STING ferroptosis
    Article Snippet: eNOS , Cell Signaling Technology , Cat#9572; RRID: AB_10693928. .. p-eNOS (Ser1177) , Cell Signaling Technology , Cat#9571; RRID: AB_329837. .. β-Tubulin , Proteintech , Cat#10068-1-AP; RRID: AB_2288035.

    Article Title: Piezo1 activates nitric oxide synthase in red blood cells via protein kinase C with increased activity in diabetes
    Article Snippet: .. p-eNOS (Ser1177) , HUVEC , 1:1000 , 9571S; Cell Signaling Technology , Rabbit; 1:2000 (W4011; Promega). ..



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    Cell Signaling Technology Inc p enos
    Characterization of microplastics in human penile tissues and PET-MP-induced functional and histological alterations in a rat model (A) Proportional distribution of common MP types in penile tissue samples from patients with Penile-CA and ED-IPP. (B) Quantification of PET levels in penile tissues from the two groups. (C) Representative intracavernosal pressure (ICP) and mean arterial pressure (MAP) traces. (D) ICP/MAP ratio in the control, L-MP, and H-MP groups. (E) Masson’s trichrome staining of CC tissue; scale bars, 150 μm. (F) Quantification of smooth muscle-to-collagen ratio. (G) Western blot analysis of <t>eNOS,</t> p -eNOS, TGF-β1, and α-SMA. (H) IF staining of eNOS, TGF-β1, and α-SMA in penile tissue; scale bars, 50 μm. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.
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    Characterization of microplastics in human penile tissues and PET-MP-induced functional and histological alterations in a rat model (A) Proportional distribution of common MP types in penile tissue samples from patients with Penile-CA and ED-IPP. (B) Quantification of PET levels in penile tissues from the two groups. (C) Representative intracavernosal pressure (ICP) and mean arterial pressure (MAP) traces. (D) ICP/MAP ratio in the control, L-MP, and H-MP groups. (E) Masson’s trichrome staining of CC tissue; scale bars, 150 μm. (F) Quantification of smooth muscle-to-collagen ratio. (G) Western blot analysis of <t>eNOS,</t> p -eNOS, TGF-β1, and α-SMA. (H) IF staining of eNOS, TGF-β1, and α-SMA in penile tissue; scale bars, 50 μm. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.
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    Characterization of microplastics in human penile tissues and PET-MP-induced functional and histological alterations in a rat model (A) Proportional distribution of common MP types in penile tissue samples from patients with Penile-CA and ED-IPP. (B) Quantification of PET levels in penile tissues from the two groups. (C) Representative intracavernosal pressure (ICP) and mean arterial pressure (MAP) traces. (D) ICP/MAP ratio in the control, L-MP, and H-MP groups. (E) Masson’s trichrome staining of CC tissue; scale bars, 150 μm. (F) Quantification of smooth muscle-to-collagen ratio. (G) Western blot analysis of <t>eNOS,</t> p -eNOS, TGF-β1, and α-SMA. (H) IF staining of eNOS, TGF-β1, and α-SMA in penile tissue; scale bars, 50 μm. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.
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    Image Search Results


    Characterization of microplastics in human penile tissues and PET-MP-induced functional and histological alterations in a rat model (A) Proportional distribution of common MP types in penile tissue samples from patients with Penile-CA and ED-IPP. (B) Quantification of PET levels in penile tissues from the two groups. (C) Representative intracavernosal pressure (ICP) and mean arterial pressure (MAP) traces. (D) ICP/MAP ratio in the control, L-MP, and H-MP groups. (E) Masson’s trichrome staining of CC tissue; scale bars, 150 μm. (F) Quantification of smooth muscle-to-collagen ratio. (G) Western blot analysis of eNOS, p -eNOS, TGF-β1, and α-SMA. (H) IF staining of eNOS, TGF-β1, and α-SMA in penile tissue; scale bars, 50 μm. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.

    Journal: iScience

    Article Title: Polyethylene terephthalate microplastics impair erectile function through macrophage mediated cGAS-STING ferroptosis

    doi: 10.1016/j.isci.2026.115044

    Figure Lengend Snippet: Characterization of microplastics in human penile tissues and PET-MP-induced functional and histological alterations in a rat model (A) Proportional distribution of common MP types in penile tissue samples from patients with Penile-CA and ED-IPP. (B) Quantification of PET levels in penile tissues from the two groups. (C) Representative intracavernosal pressure (ICP) and mean arterial pressure (MAP) traces. (D) ICP/MAP ratio in the control, L-MP, and H-MP groups. (E) Masson’s trichrome staining of CC tissue; scale bars, 150 μm. (F) Quantification of smooth muscle-to-collagen ratio. (G) Western blot analysis of eNOS, p -eNOS, TGF-β1, and α-SMA. (H) IF staining of eNOS, TGF-β1, and α-SMA in penile tissue; scale bars, 50 μm. ∗ p < 0.05, ∗∗ p < 0.01, and ∗∗∗ p < 0.001.

    Article Snippet: Equal amounts of protein (30 μg) were separated on 10% SDS-PAGE gels at 120 V for 2 h and transferred onto NC membranes at 400 mA for 1 h. Membranes were blocked with 5% non-fat milk at room temperature for 2 h and incubated overnight at 4°C with primary antibodies against TGF-β (Abcam, ab92486, 1:1000), α-SMA (Abcam, ab7817, 1:5000), eNOS (Cell Signaling Technology, CST #9572, 1:1000), p-eNOS (CST #9571, 1:1000), β-tubulin (Proteintech, 10068-1-AP, 1:5000), IL-1β (CST #12703, 1:1000), IL-6 (CST #12912, 1:1000), TNF-α (Abcam, ab6671, 1:1000), PPARα (Abcam, ab8934, 1:1000), PGC-1α (Abcam, ab54481, 1:1000), SDHB (Proteintech, 10620-1-AP, 1:2000), cGAS (CST #31659, 1:1000), STING (CST #13647, 1:1000), GPX4 (Abcam, ab125066, 1:1000), E-cadherin (CST #3195, 1:1000), Smad2 (CST #5339, 1:1000), Smad3 (CST #9523, 1:1000), p-Smad2 (CST #3108, 1:1000), p-Smad3 (CST #9520, 1:1000), CD31 (Abcam, ab28364, 1:1000), and FSP1 (Abcam, ab218163, 1:1000).

    Techniques: Functional Assay, Control, Staining, Western Blot