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α smooth muscle actin α sma  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc α smooth muscle actin α sma
    α Smooth Muscle Actin α Sma, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 98/100, based on 1771 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+%CE%B1+smooth+muscle+actin+%CE%B1+sma/alpha-Smooth+Muscle+Actin+XP+Rabbit+mAb/pm41901327-121-7-16
    Average 98 stars, based on 1771 article reviews
    α smooth muscle actin α sma - by Bioz Stars, 2026-09
    98/100 stars

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    Related Articles

    Immunostaining:

    Article Title: EphA2 blockage ALW-II-41-27 alleviates atherosclerosis by remodeling gut microbiota to regulate bile acid metabolism
    Article Snippet: .. For immunostaining, the following primary antibodies were applied: rat anti-F4/80 (abcam, ab6640; diluted 1:200), rabbit anti-CD68 (Cell Signaling Technology, 97778S; diluted 1:200), rabbit anti-α-smooth muscle actin (α-SMA) (Cell Signaling Technology, 19245S; diluted 1:400), rabbit anti-phospho-NF-κB p65 (Cell Signaling Technology, 3033S; diluted 1:1000), and rabbit anti-inducible nitric oxide synthase (iNOS) (diluted 1:400, ab178945). ..

    Incubation:

    Article Title: Fibrotic changes in the infrapatellar fat pad induce new vessel formation and sensory nerve fiber endings that associate prolonged pain.
    Article Snippet: The infrapatellar fat pad (IFP) contains nerve fiber endings and is considered to play an important role in the perception of knee pain.. However, it is unclear whether and to what degree prolonged pain influences the nociceptive role of the IFP.. To answer this question, we established a novel rat model of knee pain in which inflammation is restricted to the IFP.

    Article Title: CPNE1: A novel therapeutic target for myopia progression - from genetic GWAS discovery to functional validation in vitro and vivo.
    Article Snippet: Proteins (13 μL per sample) alongside a multi-colored pre-stained molecular weight marker (EpiZyme, China) were separated on a 10% SDS-PAGE gel and transferred to polyvinylidene fluoride membranes. .. After blocking AR TIC LE IN PR ES S with 5% nonfat dry milk, the membranes were incubated overnight at 4°C with primary antibodies, including rabbit anti-CPNE1 (1:1000, Abcam), mouse anti-β-actin (1:3000, Proteintech), rabbit anti-α-smooth muscle actin (α-SMA) (1:1000, CST), and rabbit antiPLCγ1 (1:1000, CST). .. The membranes were then washed and incubated with corresponding horseradish peroxidase-conjugated secondary antibodies (1:10000 for anti-rabbit IgG, 1:5000 for antimouse IgG; Proteintech) at room temperature for 2 h. Protein bands were visualized using enhanced chemiluminescence (Engreen) and analyzed with ImageJ.

    Staining:

    Article Title: Intratracheal administration of umbilical cord-derived mesenchymal stem cells attenuates hyperoxia-induced multi-organ injury via heme oxygenase-1 and JAK/STAT pathways
    Article Snippet: .. Subsequently, the samples were stained with rabbit anti-α smooth muscle actin (α-SMA) antibody (1:100; 19245S, CST, Danvers, MA, United States), or rabbit anti-von Willebrand factor (vWF) polyclonal antibody (1:50; 27186-1-AP, Proteintech, Rosemont, IL, United States) as primary antibodies overnight at 4 °C. .. For IHC, sections were then incubated with horseradish peroxidase (HRP)-labeled goat anti-rabbit/mouse IgG polymers (PK10006, Proteintech), developed in 3,3′-diaminobenzidine (Proteintech) and counterstained with hematoxylin following the manufacturer’s recommendations.

    Blocking Assay:

    Article Title: CPNE1: A novel therapeutic target for myopia progression - from genetic GWAS discovery to functional validation in vitro and vivo.
    Article Snippet: Proteins (13 μL per sample) alongside a multi-colored pre-stained molecular weight marker (EpiZyme, China) were separated on a 10% SDS-PAGE gel and transferred to polyvinylidene fluoride membranes. .. After blocking AR TIC LE IN PR ES S with 5% nonfat dry milk, the membranes were incubated overnight at 4°C with primary antibodies, including rabbit anti-CPNE1 (1:1000, Abcam), mouse anti-β-actin (1:3000, Proteintech), rabbit anti-α-smooth muscle actin (α-SMA) (1:1000, CST), and rabbit antiPLCγ1 (1:1000, CST). .. The membranes were then washed and incubated with corresponding horseradish peroxidase-conjugated secondary antibodies (1:10000 for anti-rabbit IgG, 1:5000 for antimouse IgG; Proteintech) at room temperature for 2 h. Protein bands were visualized using enhanced chemiluminescence (Engreen) and analyzed with ImageJ.



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    Effect of 3-CP on ROS content and activation of HSCs. ( A - B ) Fluorescence intensity of DCFH-DA in LX2 cells recorded by fluorescence microscope and flow cytometry (scar bar: 100 μm). ( C ) Relative fluorescence intensity of LX2 cells according to flow cytometry. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group. ( D - E ) qRT-PCR analysis of the effects of 3-CP on the levels <t>of</t> <t>α-SMA</t> and type I collagen in LX2 induced by LPS. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group.
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    Effect of 3-CP on ROS content and activation of HSCs. ( A - B ) Fluorescence intensity of DCFH-DA in LX2 cells recorded by fluorescence microscope and flow cytometry (scar bar: 100 μm). ( C ) Relative fluorescence intensity of LX2 cells according to flow cytometry. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group. ( D - E ) qRT-PCR analysis of the effects of 3-CP on the levels <t>of</t> <t>α-SMA</t> and type I collagen in LX2 induced by LPS. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group.
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    Effect of 3-CP on ROS content and activation of HSCs. ( A - B ) Fluorescence intensity of DCFH-DA in LX2 cells recorded by fluorescence microscope and flow cytometry (scar bar: 100 μm). ( C ) Relative fluorescence intensity of LX2 cells according to flow cytometry. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group. ( D - E ) qRT-PCR analysis of the effects of 3-CP on the levels <t>of</t> <t>α-SMA</t> and type I collagen in LX2 induced by LPS. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group.
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    Cell Signaling Technology Inc anti α sma
    Effect of 3-CP on ROS content and activation of HSCs. ( A - B ) Fluorescence intensity of DCFH-DA in LX2 cells recorded by fluorescence microscope and flow cytometry (scar bar: 100 μm). ( C ) Relative fluorescence intensity of LX2 cells according to flow cytometry. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group. ( D - E ) qRT-PCR analysis of the effects of 3-CP on the levels <t>of</t> <t>α-SMA</t> and type I collagen in LX2 induced by LPS. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group.
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    Image Search Results


    Effect of 3-CP on ROS content and activation of HSCs. ( A - B ) Fluorescence intensity of DCFH-DA in LX2 cells recorded by fluorescence microscope and flow cytometry (scar bar: 100 μm). ( C ) Relative fluorescence intensity of LX2 cells according to flow cytometry. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group. ( D - E ) qRT-PCR analysis of the effects of 3-CP on the levels of α-SMA and type I collagen in LX2 induced by LPS. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group.

    Journal: Scientific Reports

    Article Title: 3-carbamoyl proxyl nitroxide attenuates CCl 4 -induced liver fibrosis in mice through antioxidant-inflammatory regulation of TLR4/NF-κB signaling pathway

    doi: 10.1038/s41598-026-46137-1

    Figure Lengend Snippet: Effect of 3-CP on ROS content and activation of HSCs. ( A - B ) Fluorescence intensity of DCFH-DA in LX2 cells recorded by fluorescence microscope and flow cytometry (scar bar: 100 μm). ( C ) Relative fluorescence intensity of LX2 cells according to flow cytometry. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group. ( D - E ) qRT-PCR analysis of the effects of 3-CP on the levels of α-SMA and type I collagen in LX2 induced by LPS. Data are shown as mean ± SD, n = 3. * p < 0.05 vs. control group; # p < 0.05 vs. LPS group.

    Article Snippet: Primary antibodies against NF-κB p65 (Cat #8242S), α-SMA (Cat# 19245 S), collagen I (Cat# 72026 S) and secondary antibody anti-rabbit IgG (CST#7074S) were purchased from Cell Signaling Technology (Danvers, MA, United States).

    Techniques: Activation Assay, Fluorescence, Microscopy, Flow Cytometry, Control, Quantitative RT-PCR

    3-CP alleviated CCl 4 -induced liver fibrosis in mice. ( A ) Representative results and staining intensity scores of immunohistochemical staining forα-smooth muscle actin (α-SMA) and collagen I in the liver (20x, scar bar: 200 μm; 40x, scar bar: 100 μm). ( B ) Representative Western blot images showing protein expression of α-SMA, collagen I, and GAPDH. ( C ) Quantification of α-SMA protein expression. Data are presented as mean ± SD, n = 3. * p < 0.05, vs. control group; # p < 0.05, vs. model group. ( D ) Quantification of collagen I protein expression. Data are presented as mean ± SD, n = 3. * p < 0.05, vs. control group; # p < 0.05, vs. model group. ( E ) Serum index levels of liver function, and ALT and AST levels. ( F ) Levels of inflammatory factors (IL-1β and IL-6) were detected by ELISA. Data are presented as mean ± SD, n = 3. * p < 0.05, vs. control group; # p < 0.05, vs. model group.

    Journal: Scientific Reports

    Article Title: 3-carbamoyl proxyl nitroxide attenuates CCl 4 -induced liver fibrosis in mice through antioxidant-inflammatory regulation of TLR4/NF-κB signaling pathway

    doi: 10.1038/s41598-026-46137-1

    Figure Lengend Snippet: 3-CP alleviated CCl 4 -induced liver fibrosis in mice. ( A ) Representative results and staining intensity scores of immunohistochemical staining forα-smooth muscle actin (α-SMA) and collagen I in the liver (20x, scar bar: 200 μm; 40x, scar bar: 100 μm). ( B ) Representative Western blot images showing protein expression of α-SMA, collagen I, and GAPDH. ( C ) Quantification of α-SMA protein expression. Data are presented as mean ± SD, n = 3. * p < 0.05, vs. control group; # p < 0.05, vs. model group. ( D ) Quantification of collagen I protein expression. Data are presented as mean ± SD, n = 3. * p < 0.05, vs. control group; # p < 0.05, vs. model group. ( E ) Serum index levels of liver function, and ALT and AST levels. ( F ) Levels of inflammatory factors (IL-1β and IL-6) were detected by ELISA. Data are presented as mean ± SD, n = 3. * p < 0.05, vs. control group; # p < 0.05, vs. model group.

    Article Snippet: Primary antibodies against NF-κB p65 (Cat #8242S), α-SMA (Cat# 19245 S), collagen I (Cat# 72026 S) and secondary antibody anti-rabbit IgG (CST#7074S) were purchased from Cell Signaling Technology (Danvers, MA, United States).

    Techniques: Staining, Immunohistochemical staining, Western Blot, Expressing, Control, Enzyme-linked Immunosorbent Assay