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smoothelin  (Novus Biologicals)


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    Structured Review

    Novus Biologicals smoothelin
    ( A ) To visualize SMCs, transverse sections of whole cervices from days 12, 15, 17, and 19 gravid mice ( n ≥ 3) were immunofluoresently stained with specific markers for a contractile (MYH11 and <t>SMTN)</t> or synthetic phenotype (RBP1 and MYH10). Sections were also stained with CNN1 and α-SMA, which are markers of contractile smooth muscle and myofibroblasts. The grayscale bar (left) is a schematic representation of markers associated with a particular SMC phenotype. Green indicates positive immunostaining for each marker; blue indicates nuclei counterstained with 4′,6-diamidino-2-phenylindole (DAPI). ( B ) Control immunoglobulin G (IgG; left) was used as a control for the primary antibodies, and primary antibodies were omitted as controls for the secondary antibodies. Representative dual immunostaining of MYH10 (green) and MYH11 (red). Scale bars, 1000 μm; inset scale bars, 60 μm. Inset depicts high-power view of select regions (dashed box) of interest, which show longitudinal- and circumferentially oriented contractile SMCs, as well as synthetic SMCs in the broad subepithelial region and diffusely throughout the stroma.
    Smoothelin, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 92/100, based on 5 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/smoothelin/Smoothelin+Antibody/pmc11654679-263-41-43
    Average 92 stars, based on 5 article reviews
    smoothelin - by Bioz Stars, 2026-09
    92/100 stars

    Images

    1) Product Images from "Regional differences in three-dimensional fiber organization, smooth muscle cell phenotype, and contractility in the pregnant mouse cervix"

    Article Title: Regional differences in three-dimensional fiber organization, smooth muscle cell phenotype, and contractility in the pregnant mouse cervix

    Journal: Science Advances

    doi: 10.1126/sciadv.adr3530

    ( A ) To visualize SMCs, transverse sections of whole cervices from days 12, 15, 17, and 19 gravid mice ( n ≥ 3) were immunofluoresently stained with specific markers for a contractile (MYH11 and SMTN) or synthetic phenotype (RBP1 and MYH10). Sections were also stained with CNN1 and α-SMA, which are markers of contractile smooth muscle and myofibroblasts. The grayscale bar (left) is a schematic representation of markers associated with a particular SMC phenotype. Green indicates positive immunostaining for each marker; blue indicates nuclei counterstained with 4′,6-diamidino-2-phenylindole (DAPI). ( B ) Control immunoglobulin G (IgG; left) was used as a control for the primary antibodies, and primary antibodies were omitted as controls for the secondary antibodies. Representative dual immunostaining of MYH10 (green) and MYH11 (red). Scale bars, 1000 μm; inset scale bars, 60 μm. Inset depicts high-power view of select regions (dashed box) of interest, which show longitudinal- and circumferentially oriented contractile SMCs, as well as synthetic SMCs in the broad subepithelial region and diffusely throughout the stroma.
    Figure Legend Snippet: ( A ) To visualize SMCs, transverse sections of whole cervices from days 12, 15, 17, and 19 gravid mice ( n ≥ 3) were immunofluoresently stained with specific markers for a contractile (MYH11 and SMTN) or synthetic phenotype (RBP1 and MYH10). Sections were also stained with CNN1 and α-SMA, which are markers of contractile smooth muscle and myofibroblasts. The grayscale bar (left) is a schematic representation of markers associated with a particular SMC phenotype. Green indicates positive immunostaining for each marker; blue indicates nuclei counterstained with 4′,6-diamidino-2-phenylindole (DAPI). ( B ) Control immunoglobulin G (IgG; left) was used as a control for the primary antibodies, and primary antibodies were omitted as controls for the secondary antibodies. Representative dual immunostaining of MYH10 (green) and MYH11 (red). Scale bars, 1000 μm; inset scale bars, 60 μm. Inset depicts high-power view of select regions (dashed box) of interest, which show longitudinal- and circumferentially oriented contractile SMCs, as well as synthetic SMCs in the broad subepithelial region and diffusely throughout the stroma.

    Techniques Used: Staining, Immunostaining, Marker, Control

    Related Articles

    Incubation:

    Article Title: Regional differences in three-dimensional fiber organization, smooth muscle cell phenotype, and contractility in the pregnant mouse cervix
    Article Snippet: For immunofluorescent staining, sections were fixed with 2% paraformaldehyde (Electron Microscopy Sciences) for 20 min. After washing with 1× PBS, sections were incubated for 1 hour at room temperature using blocking solution (10% goat serum and 0.25% Triton X-100 in 1X PBS). .. Sections were incubated overnight at 4°C with blocking solution containing the following primary antibodies: calponin (1:200 dilution; Abcam, ab46794), MYH10 (1:50; Cell Signaling Technologies, 3404), MYH11 (1:125; Abcam, ab224804), RBP1 (1:100, Abcam ab154881), α-SMA (1:200 dilution; Cell Signaling Technologies, 19245), or smoothelin (1:100; Novus Biologicals, NBP2-37931). .. After washing with 1× PBS, samples were incubated with fluorescent-labeled secondary antibody (1:1000; Invitrogen, A-11008) and 4′,6-diamidino-2-phenylindole (DAPI) for 2 hours at room temperature.

    Article Title: Regional differences in three-dimensional fiber organization, smooth muscle cell phenotype, and contractility in the pregnant mouse cervix.
    Article Snippet: For immunofluorescent staining, sections were fixed with 2% paraformaldehyde (Electron Microscopy Sciences) for 20 min. After washing with 1× PBS, sections were incubated for 1 hour at room temperature using blocking solution (10% goat serum and 0.25% Triton X- 100 in 1X PBS). .. Sections were incubated overnight at 4°C with blocking solution containing the following primary antibodies: calponin (1:200 dilution; Abcam, ab46794), MYH10 (1:50; Cell Signaling Technologies, 3404), MYH11 (1:125; Abcam, ab224804), RBP1 (1:100, Abcam ab154881), α- SMA (1:200 dilution; Cell Signaling Technologies, 19245), or smoothelin (1:100; Novus Biologicals, NBP2- 37931). .. After washing with 1× PBS, samples were incubated with fluorescent- labeled secondary antibody (1:1000; Invitrogen, A11008) and 4′,6- diamidino- 2- phenylindole (DAPI) for 2 hours at room temperature.

    Article Title: Mid-old cells are a potential target for anti-aging interventions in the elderly
    Article Snippet: Counterstaining of each stained slide was performed using Hematoxylin II (790-2208, Ventana Medical Sytems Inc.). .. For IF staining of FFPE tissue sections, the following primary antibodies were incubated overnight at 4 °C: SAA1, 1:50 (MAB30191, R&D Systems); p21 Waf1 , 1:100 (ab109520, Abcam); IL1β, 1:100 (ab9722, Abcam); SLIT2, 1:200 (PA5-31133, Invitrogen); p16 INK4A , predilution (805-4713, Roche); Vimentin, 1:400 (ab92547, Abcam); Vimentin, 1:100 (AF2105, R&D Systems); Smoothelin, 1:100 (OMA1-06020, Invitrogen); Smoothelin, 1:500 (NBP2-37931, Novus Biologicals); E-cadherin, 1:200 (610181, Becton Dickinson); E-cadherin, 1:100 (ab15148, Abcam); CDX2, 1:100, (235R-15, Cell Margue, Rocklin, CA). ..

    Blocking Assay:

    Article Title: Regional differences in three-dimensional fiber organization, smooth muscle cell phenotype, and contractility in the pregnant mouse cervix
    Article Snippet: For immunofluorescent staining, sections were fixed with 2% paraformaldehyde (Electron Microscopy Sciences) for 20 min. After washing with 1× PBS, sections were incubated for 1 hour at room temperature using blocking solution (10% goat serum and 0.25% Triton X-100 in 1X PBS). .. Sections were incubated overnight at 4°C with blocking solution containing the following primary antibodies: calponin (1:200 dilution; Abcam, ab46794), MYH10 (1:50; Cell Signaling Technologies, 3404), MYH11 (1:125; Abcam, ab224804), RBP1 (1:100, Abcam ab154881), α-SMA (1:200 dilution; Cell Signaling Technologies, 19245), or smoothelin (1:100; Novus Biologicals, NBP2-37931). .. After washing with 1× PBS, samples were incubated with fluorescent-labeled secondary antibody (1:1000; Invitrogen, A-11008) and 4′,6-diamidino-2-phenylindole (DAPI) for 2 hours at room temperature.

    Article Title: Regional differences in three-dimensional fiber organization, smooth muscle cell phenotype, and contractility in the pregnant mouse cervix.
    Article Snippet: For immunofluorescent staining, sections were fixed with 2% paraformaldehyde (Electron Microscopy Sciences) for 20 min. After washing with 1× PBS, sections were incubated for 1 hour at room temperature using blocking solution (10% goat serum and 0.25% Triton X- 100 in 1X PBS). .. Sections were incubated overnight at 4°C with blocking solution containing the following primary antibodies: calponin (1:200 dilution; Abcam, ab46794), MYH10 (1:50; Cell Signaling Technologies, 3404), MYH11 (1:125; Abcam, ab224804), RBP1 (1:100, Abcam ab154881), α- SMA (1:200 dilution; Cell Signaling Technologies, 19245), or smoothelin (1:100; Novus Biologicals, NBP2- 37931). .. After washing with 1× PBS, samples were incubated with fluorescent- labeled secondary antibody (1:1000; Invitrogen, A11008) and 4′,6- diamidino- 2- phenylindole (DAPI) for 2 hours at room temperature.

    Staining:

    Article Title: Mid-old cells are a potential target for anti-aging interventions in the elderly
    Article Snippet: Counterstaining of each stained slide was performed using Hematoxylin II (790-2208, Ventana Medical Sytems Inc.). .. For IF staining of FFPE tissue sections, the following primary antibodies were incubated overnight at 4 °C: SAA1, 1:50 (MAB30191, R&D Systems); p21 Waf1 , 1:100 (ab109520, Abcam); IL1β, 1:100 (ab9722, Abcam); SLIT2, 1:200 (PA5-31133, Invitrogen); p16 INK4A , predilution (805-4713, Roche); Vimentin, 1:400 (ab92547, Abcam); Vimentin, 1:100 (AF2105, R&D Systems); Smoothelin, 1:100 (OMA1-06020, Invitrogen); Smoothelin, 1:500 (NBP2-37931, Novus Biologicals); E-cadherin, 1:200 (610181, Becton Dickinson); E-cadherin, 1:100 (ab15148, Abcam); CDX2, 1:100, (235R-15, Cell Margue, Rocklin, CA). ..

    Formalin-fixed Paraffin-Embedded:

    Article Title: Mid-old cells are a potential target for anti-aging interventions in the elderly
    Article Snippet: Counterstaining of each stained slide was performed using Hematoxylin II (790-2208, Ventana Medical Sytems Inc.). .. For IF staining of FFPE tissue sections, the following primary antibodies were incubated overnight at 4 °C: SAA1, 1:50 (MAB30191, R&D Systems); p21 Waf1 , 1:100 (ab109520, Abcam); IL1β, 1:100 (ab9722, Abcam); SLIT2, 1:200 (PA5-31133, Invitrogen); p16 INK4A , predilution (805-4713, Roche); Vimentin, 1:400 (ab92547, Abcam); Vimentin, 1:100 (AF2105, R&D Systems); Smoothelin, 1:100 (OMA1-06020, Invitrogen); Smoothelin, 1:500 (NBP2-37931, Novus Biologicals); E-cadherin, 1:200 (610181, Becton Dickinson); E-cadherin, 1:100 (ab15148, Abcam); CDX2, 1:100, (235R-15, Cell Margue, Rocklin, CA). ..



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    Novus Biologicals smoothelin
    ( A ) To visualize SMCs, transverse sections of whole cervices from days 12, 15, 17, and 19 gravid mice ( n ≥ 3) were immunofluoresently stained with specific markers for a contractile (MYH11 and <t>SMTN)</t> or synthetic phenotype (RBP1 and MYH10). Sections were also stained with CNN1 and α-SMA, which are markers of contractile smooth muscle and myofibroblasts. The grayscale bar (left) is a schematic representation of markers associated with a particular SMC phenotype. Green indicates positive immunostaining for each marker; blue indicates nuclei counterstained with 4′,6-diamidino-2-phenylindole (DAPI). ( B ) Control immunoglobulin G (IgG; left) was used as a control for the primary antibodies, and primary antibodies were omitted as controls for the secondary antibodies. Representative dual immunostaining of MYH10 (green) and MYH11 (red). Scale bars, 1000 μm; inset scale bars, 60 μm. Inset depicts high-power view of select regions (dashed box) of interest, which show longitudinal- and circumferentially oriented contractile SMCs, as well as synthetic SMCs in the broad subepithelial region and diffusely throughout the stroma.
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    Image Search Results


    ( A ) To visualize SMCs, transverse sections of whole cervices from days 12, 15, 17, and 19 gravid mice ( n ≥ 3) were immunofluoresently stained with specific markers for a contractile (MYH11 and SMTN) or synthetic phenotype (RBP1 and MYH10). Sections were also stained with CNN1 and α-SMA, which are markers of contractile smooth muscle and myofibroblasts. The grayscale bar (left) is a schematic representation of markers associated with a particular SMC phenotype. Green indicates positive immunostaining for each marker; blue indicates nuclei counterstained with 4′,6-diamidino-2-phenylindole (DAPI). ( B ) Control immunoglobulin G (IgG; left) was used as a control for the primary antibodies, and primary antibodies were omitted as controls for the secondary antibodies. Representative dual immunostaining of MYH10 (green) and MYH11 (red). Scale bars, 1000 μm; inset scale bars, 60 μm. Inset depicts high-power view of select regions (dashed box) of interest, which show longitudinal- and circumferentially oriented contractile SMCs, as well as synthetic SMCs in the broad subepithelial region and diffusely throughout the stroma.

    Journal: Science Advances

    Article Title: Regional differences in three-dimensional fiber organization, smooth muscle cell phenotype, and contractility in the pregnant mouse cervix

    doi: 10.1126/sciadv.adr3530

    Figure Lengend Snippet: ( A ) To visualize SMCs, transverse sections of whole cervices from days 12, 15, 17, and 19 gravid mice ( n ≥ 3) were immunofluoresently stained with specific markers for a contractile (MYH11 and SMTN) or synthetic phenotype (RBP1 and MYH10). Sections were also stained with CNN1 and α-SMA, which are markers of contractile smooth muscle and myofibroblasts. The grayscale bar (left) is a schematic representation of markers associated with a particular SMC phenotype. Green indicates positive immunostaining for each marker; blue indicates nuclei counterstained with 4′,6-diamidino-2-phenylindole (DAPI). ( B ) Control immunoglobulin G (IgG; left) was used as a control for the primary antibodies, and primary antibodies were omitted as controls for the secondary antibodies. Representative dual immunostaining of MYH10 (green) and MYH11 (red). Scale bars, 1000 μm; inset scale bars, 60 μm. Inset depicts high-power view of select regions (dashed box) of interest, which show longitudinal- and circumferentially oriented contractile SMCs, as well as synthetic SMCs in the broad subepithelial region and diffusely throughout the stroma.

    Article Snippet: Sections were incubated overnight at 4°C with blocking solution containing the following primary antibodies: calponin (1:200 dilution; Abcam, ab46794), MYH10 (1:50; Cell Signaling Technologies, 3404), MYH11 (1:125; Abcam, ab224804), RBP1 (1:100, Abcam ab154881), α-SMA (1:200 dilution; Cell Signaling Technologies, 19245), or smoothelin (1:100; Novus Biologicals, NBP2-37931).

    Techniques: Staining, Immunostaining, Marker, Control