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Santa Cruz Biotechnology anti desmin mouse monoclonal antibody
Myogenic differentiation of bMuSCs and formation of cultured meat construct on a P . ferulae dECM scaffold. (A) Schematic illustrating the timeline for the proliferation and subsequent myogenic differentiation of bMuSCs on the scaffold. Created with BioRender.com . (B) Quantitative real-time polymerase chain reaction (qPCR) analysis of muscle-specific gene expression ( MYOG , MYOD1 and MYH7 ) in bMuSCs before and after differentiation on P . ferulae dECM scaffold. Data are presented as mean ± SD ( n = 3), with statistical significance determined by a Student's t -test (∗∗∗ p < 0.005). (C) Comparative histological analysis of the tissue structure with and without bMuSCs on P . ferulae dECM scaffolds by H&E staining. Scale bar = 200 μm. (D) Immunofluorescence images of bMuSCs after myogenic differentiation on P . ferulae dECM scaffolds, showing myotube formation via myogenic proteins <t>Desmin</t> (green) and MYF6 (red) expression. Nuclei are counterstained with DAPI (blue). Scale bar = 100 μm. (E) Quantification of the percentage of cells expressing Desmin and MYF6, respectively, relative to the total number of cells (DAPI-stained nuclei). (F) Fusion index calculated as the percentage of total nuclei residing within myotubes containing ≥2 nuclei. Data are presented as mean ± SD ( n = 3). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
Anti Desmin Mouse Monoclonal Antibody, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Myogenic differentiation of bMuSCs and formation of cultured meat construct on a P . ferulae dECM scaffold. (A) Schematic illustrating the timeline for the proliferation and subsequent myogenic differentiation of bMuSCs on the scaffold. Created with BioRender.com . (B) Quantitative real-time polymerase chain reaction (qPCR) analysis of muscle-specific gene expression ( MYOG , MYOD1 and MYH7 ) in bMuSCs before and after differentiation on P . ferulae dECM scaffold. Data are presented as mean ± SD ( n = 3), with statistical significance determined by a Student's t -test (∗∗∗ p < 0.005). (C) Comparative histological analysis of the tissue structure with and without bMuSCs on P . ferulae dECM scaffolds by H&E staining. Scale bar = 200 μm. (D) Immunofluorescence images of bMuSCs after myogenic differentiation on P . ferulae dECM scaffolds, showing myotube formation via myogenic proteins Desmin (green) and MYF6 (red) expression. Nuclei are counterstained with DAPI (blue). Scale bar = 100 μm. (E) Quantification of the percentage of cells expressing Desmin and MYF6, respectively, relative to the total number of cells (DAPI-stained nuclei). (F) Fusion index calculated as the percentage of total nuclei residing within myotubes containing ≥2 nuclei. Data are presented as mean ± SD ( n = 3). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Journal: Materials Today Bio

Article Title: Decellularized extracellular matrix scaffolds from Pleurotus ferulae mushrooms for sustainable production of steak-like cultured meat with authentic texture

doi: 10.1016/j.mtbio.2025.102327

Figure Lengend Snippet: Myogenic differentiation of bMuSCs and formation of cultured meat construct on a P . ferulae dECM scaffold. (A) Schematic illustrating the timeline for the proliferation and subsequent myogenic differentiation of bMuSCs on the scaffold. Created with BioRender.com . (B) Quantitative real-time polymerase chain reaction (qPCR) analysis of muscle-specific gene expression ( MYOG , MYOD1 and MYH7 ) in bMuSCs before and after differentiation on P . ferulae dECM scaffold. Data are presented as mean ± SD ( n = 3), with statistical significance determined by a Student's t -test (∗∗∗ p < 0.005). (C) Comparative histological analysis of the tissue structure with and without bMuSCs on P . ferulae dECM scaffolds by H&E staining. Scale bar = 200 μm. (D) Immunofluorescence images of bMuSCs after myogenic differentiation on P . ferulae dECM scaffolds, showing myotube formation via myogenic proteins Desmin (green) and MYF6 (red) expression. Nuclei are counterstained with DAPI (blue). Scale bar = 100 μm. (E) Quantification of the percentage of cells expressing Desmin and MYF6, respectively, relative to the total number of cells (DAPI-stained nuclei). (F) Fusion index calculated as the percentage of total nuclei residing within myotubes containing ≥2 nuclei. Data are presented as mean ± SD ( n = 3). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

Article Snippet: The primary antibodies used were an anti-desmin mouse monoclonal antibody (sc-23877; Santa Cruz Biotechnology, Dallas, TX, USA) and an anti-myogenic factor 6 (Myf-6) goat polyclonal antibody (NB100-1489; Novus Biologicals, Centennial, CO, USA).

Techniques: Cell Culture, Construct, Real-time Polymerase Chain Reaction, Gene Expression, Staining, Immunofluorescence, Expressing