Review



immunofluorescence staining for desmin  (Proteintech)


Bioz Verified Symbol Proteintech is a verified supplier  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 95

    Structured Review

    Proteintech immunofluorescence staining for desmin
    Characterization of CCSMCs and their interaction with exosomes . (A) Primary CCSMCs migrating from cavernous tissue explants. (B) <t>Immunofluorescence</t> staining with anti-α-SMA and <t>anti-Desmin</t> antibodies confirming the identity of CCSMCs. (C) Internalization of PKH67-labeled Exo and Exo-145 by CCSMCs, showing green fluorescence within the cytoplasm. (D) Elevated miR-145 expression levels in CCSMCs after co-culture with Exo or Exo-145. Data are presented as mean ± SEM. ∗∗∗ p < 0.001, ns: no significant difference.
    Immunofluorescence Staining For Desmin, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 131 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/immunofluorescence staining for desmin/product/Proteintech
    Average 95 stars, based on 131 article reviews
    immunofluorescence staining for desmin - by Bioz Stars, 2026-02
    95/100 stars

    Images

    1) Product Images from "miR-145-enriched BMSCs-derived exosomes ameliorate neurogenic erectile dysfunction in aged rats via TGFBR2 inhibition"

    Article Title: miR-145-enriched BMSCs-derived exosomes ameliorate neurogenic erectile dysfunction in aged rats via TGFBR2 inhibition

    Journal: Regenerative Therapy

    doi: 10.1016/j.reth.2025.04.004

    Characterization of CCSMCs and their interaction with exosomes . (A) Primary CCSMCs migrating from cavernous tissue explants. (B) Immunofluorescence staining with anti-α-SMA and anti-Desmin antibodies confirming the identity of CCSMCs. (C) Internalization of PKH67-labeled Exo and Exo-145 by CCSMCs, showing green fluorescence within the cytoplasm. (D) Elevated miR-145 expression levels in CCSMCs after co-culture with Exo or Exo-145. Data are presented as mean ± SEM. ∗∗∗ p < 0.001, ns: no significant difference.
    Figure Legend Snippet: Characterization of CCSMCs and their interaction with exosomes . (A) Primary CCSMCs migrating from cavernous tissue explants. (B) Immunofluorescence staining with anti-α-SMA and anti-Desmin antibodies confirming the identity of CCSMCs. (C) Internalization of PKH67-labeled Exo and Exo-145 by CCSMCs, showing green fluorescence within the cytoplasm. (D) Elevated miR-145 expression levels in CCSMCs after co-culture with Exo or Exo-145. Data are presented as mean ± SEM. ∗∗∗ p < 0.001, ns: no significant difference.

    Techniques Used: Immunofluorescence, Staining, Labeling, Fluorescence, Expressing, Co-Culture Assay



    Similar Products

    95
    Proteintech immunofluorescence staining for desmin
    Characterization of CCSMCs and their interaction with exosomes . (A) Primary CCSMCs migrating from cavernous tissue explants. (B) <t>Immunofluorescence</t> staining with anti-α-SMA and <t>anti-Desmin</t> antibodies confirming the identity of CCSMCs. (C) Internalization of PKH67-labeled Exo and Exo-145 by CCSMCs, showing green fluorescence within the cytoplasm. (D) Elevated miR-145 expression levels in CCSMCs after co-culture with Exo or Exo-145. Data are presented as mean ± SEM. ∗∗∗ p < 0.001, ns: no significant difference.
    Immunofluorescence Staining For Desmin, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/immunofluorescence staining for desmin/product/Proteintech
    Average 95 stars, based on 1 article reviews
    immunofluorescence staining for desmin - by Bioz Stars, 2026-02
    95/100 stars
      Buy from Supplier

    95
    Proteintech immunofluorescence staining
    Figure 1. Characterization of the solid or porous Se@SiO2 NPs and identification of satellite cells. (A) Fabrication process of porous Se@SiO2 NPs. (B) x-ray diffractometer pattern of the solid Se@SiO2 NPs and the typical selenium nanocrystals (Joint Committee on Powder Diffraction Standards card no. 65–1,876). (C) Low and (D) high magnification of transmission electron microscopy images of the solid Se@SiO2 NPs. (E) Transmission electron microscopy images of porous Se@SiO2 NPs. (F) PAX7 and desmin were detected by <t>immunofluorescence;</t> cytoskeletal alterations were detected by staining with F-actin. The nuclei of satellite cells were stained with Hoechst. The scale bar represents 20 μm. (G) Cell proliferation in satellite cells in response to different porous Se@SiO2 NP concentrations. *p < 0.05; **p < 0.01; ***p < 0.001 compared with control (0 μg/ml). DIW: Deionized water; NP: Nanoparticle; PVP: Polyvinylpyrrolidone; TEOS: Tetraethyl orthosilicate.
    Immunofluorescence Staining, supplied by Proteintech, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/immunofluorescence staining/product/Proteintech
    Average 95 stars, based on 1 article reviews
    immunofluorescence staining - by Bioz Stars, 2026-02
    95/100 stars
      Buy from Supplier

    95
    Cell Signaling Technology Inc immunofluorescence staining
    The effect of macrophage transformation on the activation of hepatic stellate cells by <t>immunofluorescence</t> staining of α-SMA. * P < 0.05 vs. AEm group.
    Immunofluorescence Staining, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/immunofluorescence staining/product/Cell Signaling Technology Inc
    Average 95 stars, based on 1 article reviews
    immunofluorescence staining - by Bioz Stars, 2026-02
    95/100 stars
      Buy from Supplier

    90
    Servicebio Inc desmin immunofluorescence staining
    The effect of macrophage transformation on the activation of hepatic stellate cells by <t>immunofluorescence</t> staining of α-SMA. * P < 0.05 vs. AEm group.
    Desmin Immunofluorescence Staining, supplied by Servicebio Inc, 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/desmin immunofluorescence staining/product/Servicebio Inc
    Average 90 stars, based on 1 article reviews
    desmin immunofluorescence staining - by Bioz Stars, 2026-02
    90/100 stars
      Buy from Supplier

    90
    Thermo Fisher anti-desmin immunofluorescence staining
    The effect of macrophage transformation on the activation of hepatic stellate cells by <t>immunofluorescence</t> staining of α-SMA. * P < 0.05 vs. AEm group.
    Anti Desmin Immunofluorescence Staining, supplied by Thermo Fisher, 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/anti-desmin immunofluorescence staining/product/Thermo Fisher
    Average 90 stars, based on 1 article reviews
    anti-desmin immunofluorescence staining - by Bioz Stars, 2026-02
    90/100 stars
      Buy from Supplier

    90
    Millipore anti-desmin immunofluorescent staining
    The effect of macrophage transformation on the activation of hepatic stellate cells by <t>immunofluorescence</t> staining of α-SMA. * P < 0.05 vs. AEm group.
    Anti Desmin Immunofluorescent Staining, supplied by Millipore, 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/anti-desmin immunofluorescent staining/product/Millipore
    Average 90 stars, based on 1 article reviews
    anti-desmin immunofluorescent staining - by Bioz Stars, 2026-02
    90/100 stars
      Buy from Supplier

    Image Search Results


    Characterization of CCSMCs and their interaction with exosomes . (A) Primary CCSMCs migrating from cavernous tissue explants. (B) Immunofluorescence staining with anti-α-SMA and anti-Desmin antibodies confirming the identity of CCSMCs. (C) Internalization of PKH67-labeled Exo and Exo-145 by CCSMCs, showing green fluorescence within the cytoplasm. (D) Elevated miR-145 expression levels in CCSMCs after co-culture with Exo or Exo-145. Data are presented as mean ± SEM. ∗∗∗ p < 0.001, ns: no significant difference.

    Journal: Regenerative Therapy

    Article Title: miR-145-enriched BMSCs-derived exosomes ameliorate neurogenic erectile dysfunction in aged rats via TGFBR2 inhibition

    doi: 10.1016/j.reth.2025.04.004

    Figure Lengend Snippet: Characterization of CCSMCs and their interaction with exosomes . (A) Primary CCSMCs migrating from cavernous tissue explants. (B) Immunofluorescence staining with anti-α-SMA and anti-Desmin antibodies confirming the identity of CCSMCs. (C) Internalization of PKH67-labeled Exo and Exo-145 by CCSMCs, showing green fluorescence within the cytoplasm. (D) Elevated miR-145 expression levels in CCSMCs after co-culture with Exo or Exo-145. Data are presented as mean ± SEM. ∗∗∗ p < 0.001, ns: no significant difference.

    Article Snippet: Third-generation CCSMCs were identified through immunofluorescence staining for desmin (1:200, 16520-1-AP, Proteintech) and α-smooth muscle actin (1:200, 14395-1-AP, Proteintech).

    Techniques: Immunofluorescence, Staining, Labeling, Fluorescence, Expressing, Co-Culture Assay

    Figure 1. Characterization of the solid or porous Se@SiO2 NPs and identification of satellite cells. (A) Fabrication process of porous Se@SiO2 NPs. (B) x-ray diffractometer pattern of the solid Se@SiO2 NPs and the typical selenium nanocrystals (Joint Committee on Powder Diffraction Standards card no. 65–1,876). (C) Low and (D) high magnification of transmission electron microscopy images of the solid Se@SiO2 NPs. (E) Transmission electron microscopy images of porous Se@SiO2 NPs. (F) PAX7 and desmin were detected by immunofluorescence; cytoskeletal alterations were detected by staining with F-actin. The nuclei of satellite cells were stained with Hoechst. The scale bar represents 20 μm. (G) Cell proliferation in satellite cells in response to different porous Se@SiO2 NP concentrations. *p < 0.05; **p < 0.01; ***p < 0.001 compared with control (0 μg/ml). DIW: Deionized water; NP: Nanoparticle; PVP: Polyvinylpyrrolidone; TEOS: Tetraethyl orthosilicate.

    Journal: Nanomedicine (London, England)

    Article Title: Porous Se@SiO 2 nanoparticles improve oxidative injury to promote muscle regeneration via modulating mitochondria.

    doi: 10.2217/nnm-2022-0173

    Figure Lengend Snippet: Figure 1. Characterization of the solid or porous Se@SiO2 NPs and identification of satellite cells. (A) Fabrication process of porous Se@SiO2 NPs. (B) x-ray diffractometer pattern of the solid Se@SiO2 NPs and the typical selenium nanocrystals (Joint Committee on Powder Diffraction Standards card no. 65–1,876). (C) Low and (D) high magnification of transmission electron microscopy images of the solid Se@SiO2 NPs. (E) Transmission electron microscopy images of porous Se@SiO2 NPs. (F) PAX7 and desmin were detected by immunofluorescence; cytoskeletal alterations were detected by staining with F-actin. The nuclei of satellite cells were stained with Hoechst. The scale bar represents 20 μm. (G) Cell proliferation in satellite cells in response to different porous Se@SiO2 NP concentrations. *p < 0.05; **p < 0.01; ***p < 0.001 compared with control (0 μg/ml). DIW: Deionized water; NP: Nanoparticle; PVP: Polyvinylpyrrolidone; TEOS: Tetraethyl orthosilicate.

    Article Snippet: Immunofluorescence staining With immunofluorescence staining, the expression of markers was detected using antibodies against desmin (Proteintech), PAX7 (Proteintech), MYHC (Thermo Fisher Scientific), MYOD (Invitrogen), F-actin (Abcam) and dystrophin (Santa Cruz Biotechnology, TX, USA).

    Techniques: Transmission Assay, Electron Microscopy, Immunofluorescence, Staining, Control

    Figure 7. Porous Se@SiO2 nanoparticles promote the formation of myotubes and increase the number of PAX7-positive cells. (A) Western blot analysis of MYHC, MYOD and GAPDH expression of satellite cells in each group after normalization to GAPDH expression; the comparison is shown in (B) and (C). (D) Immunofluorescence staining of MYHC was observed with dystrophin staining as background. Immunofluorescence analysis for MYHC (red) and dystrophin (green). Nuclei were stained with Hoechst, displayed in blue. The scale bar represents 20 μm. (E) Quantification of MYHC mean fluorescence intensity. (F) Representative images of PAX7 observed with dystrophin staining as background. Immunofluorescence analysis of PAX7 (red) and dystrophin (green). Nuclei were stained with Hoechst, displayed in blue. The scale bar represents 20 μm. (G) Quantification of PAX7 expression. *p < 0.05; **p < 0.01; ***p < 0.001. CTX: Cardiotoxin.

    Journal: Nanomedicine (London, England)

    Article Title: Porous Se@SiO 2 nanoparticles improve oxidative injury to promote muscle regeneration via modulating mitochondria.

    doi: 10.2217/nnm-2022-0173

    Figure Lengend Snippet: Figure 7. Porous Se@SiO2 nanoparticles promote the formation of myotubes and increase the number of PAX7-positive cells. (A) Western blot analysis of MYHC, MYOD and GAPDH expression of satellite cells in each group after normalization to GAPDH expression; the comparison is shown in (B) and (C). (D) Immunofluorescence staining of MYHC was observed with dystrophin staining as background. Immunofluorescence analysis for MYHC (red) and dystrophin (green). Nuclei were stained with Hoechst, displayed in blue. The scale bar represents 20 μm. (E) Quantification of MYHC mean fluorescence intensity. (F) Representative images of PAX7 observed with dystrophin staining as background. Immunofluorescence analysis of PAX7 (red) and dystrophin (green). Nuclei were stained with Hoechst, displayed in blue. The scale bar represents 20 μm. (G) Quantification of PAX7 expression. *p < 0.05; **p < 0.01; ***p < 0.001. CTX: Cardiotoxin.

    Article Snippet: Immunofluorescence staining With immunofluorescence staining, the expression of markers was detected using antibodies against desmin (Proteintech), PAX7 (Proteintech), MYHC (Thermo Fisher Scientific), MYOD (Invitrogen), F-actin (Abcam) and dystrophin (Santa Cruz Biotechnology, TX, USA).

    Techniques: Western Blot, Expressing, Comparison, Immunofluorescence, Staining, Fluorescence

    The effect of macrophage transformation on the activation of hepatic stellate cells by immunofluorescence staining of α-SMA. * P < 0.05 vs. AEm group.

    Journal: Bioengineered

    Article Title: Echinococcus multilocularis drives the polarization of macrophages by regulating the RhoA-MAPK signaling pathway and thus affects liver fibrosis

    doi: 10.1080/21655979.2022.2056690

    Figure Lengend Snippet: The effect of macrophage transformation on the activation of hepatic stellate cells by immunofluorescence staining of α-SMA. * P < 0.05 vs. AEm group.

    Article Snippet: Anti-desmin antibody (5332, 1:100) for immunofluorescence staining was obtained from Cell Signaling.

    Techniques: Transformation Assay, Activation Assay, Immunofluorescence, Staining