This is a Validated Antibody Database (VAD) review about rat Dmd, based on 17 published articles (read how Labome selects the articles), using Dmd antibody in all methods. It is aimed to help Labome visitors find the most suited Dmd antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
Dmd synonym: DNADMD1; dystrophin; apodystrophin-3; apodystrophin-I; dystrophin, muscular dystrophy; dystrophin-related

Knockout validation
Sigma-Aldrich
mouse monoclonal (MANDYS8)
  • western blot knockout validation; human; 1:1000; fig 5D
Sigma-Aldrich Dmd antibody (Sigma, D8168) was used in western blot knockout validation on human samples at 1:1000 (fig 5D). Nat Commun (2015) ncbi
Invitrogen
rabbit polyclonal
  • immunohistochemistry; mouse; fig 1
In order to study protection against ischemic myopathy in high fat fed mice by targeted expression of catalase to mitochondria, Invitrogen Dmd antibody (Thermo Fisher Scientific, RB-9024) was used in immunohistochemistry on mouse samples (fig 1). Diabetes (2016) ncbi
rabbit polyclonal
  • western blot; mouse; fig 1d
In order to generate and characterize a mouse model that carries a Dmd exon 2 duplication, Invitrogen Dmd antibody (Thermo Scientific, RB9024) was used in western blot on mouse samples (fig 1d). Neuromuscul Disord (2015) ncbi
rabbit polyclonal
  • immunohistochemistry - frozen section; mouse
In order to investigate mdx mice after injury and recovery of altered neuromuscular junction morphology and muscle function, Invitrogen Dmd antibody (Thermo, RB-9024-P) was used in immunohistochemistry - frozen section on mouse samples . Cell Mol Life Sci (2015) ncbi
rabbit polyclonal
  • immunohistochemistry; mouse; fig 5
In order to characterize mice deficient for obscurin, Invitrogen Dmd antibody (Thermo Fisher, RB-9024) was used in immunohistochemistry on mouse samples (fig 5). J Cell Biol (2013) ncbi
Sigma-Aldrich
mouse monoclonal (MANDRA1)
  • immunohistochemistry - frozen section; mouse; 1:300; loading ...; fig 2a
Sigma-Aldrich Dmd antibody (Sigma, MANDRA1) was used in immunohistochemistry - frozen section on mouse samples at 1:300 (fig 2a). Proc Natl Acad Sci U S A (2018) ncbi
mouse monoclonal (MANDYS8)
  • immunohistochemistry; human; 1:800; fig 3a
  • western blot; human; fig 3d
Sigma-Aldrich Dmd antibody (Sigma-Aldrich, MANDYS8) was used in immunohistochemistry on human samples at 1:800 (fig 3a) and in western blot on human samples (fig 3d). Sci Adv (2018) ncbi
mouse monoclonal (MANDRA1)
  • western blot; mouse; 1:1000; fig 6
In order to report the mechanism by which thrombospondin-4 regulates skeletal muscle integrity, Sigma-Aldrich Dmd antibody (Sigma, D8043) was used in western blot on mouse samples at 1:1000 (fig 6). elife (2016) ncbi
mouse monoclonal (MANDYS8)
  • immunohistochemistry; mouse; 1:400; fig s8
Sigma-Aldrich Dmd antibody (Sigma, D8168) was used in immunohistochemistry on mouse samples at 1:400 (fig s8). Nat Commun (2016) ncbi
mouse monoclonal (MANDYS8)
  • immunohistochemistry - frozen section; human; 1:400; fig 3
In order to study SNAP23 and colocalization with lipid droplets, mitochondria, and plasma membrane in human skeletal muscle by immunofluorescence microscopy, Sigma-Aldrich Dmd antibody (Sigma, D8168) was used in immunohistochemistry - frozen section on human samples at 1:400 (fig 3). Physiol Rep (2016) ncbi
mouse monoclonal (MANDYS8)
  • western blot; mouse; 1:200; loading ...; fig s20a
In order to present the role of in vivo genome editing in muscle function in a mouse model of Duchenne muscular dystrophy, Sigma-Aldrich Dmd antibody (Sigma-Aldrich, D8168) was used in western blot on mouse samples at 1:200 (fig s20a). Science (2016) ncbi
mouse monoclonal (MANDYS8)
  • immunohistochemistry; mouse; loading ...; fig s4a, s13b
  • western blot; mouse; 1:1000; loading ...; fig s8a, s8c, s13c
In order to present the role of postnatal genome editing in dystrophin expression in a mouse model of muscular dystrophy, Sigma-Aldrich Dmd antibody (Sigma, D8168) was used in immunohistochemistry on mouse samples (fig s4a, s13b) and in western blot on mouse samples at 1:1000 (fig s8a, s8c, s13c). Science (2016) ncbi
mouse monoclonal (MANDRA1)
  • immunohistochemistry; human; 1:100; fig 2 A-i
In order to report that resistance training leads to a decline in pericyte quantity and to an increase in mesenchymal progenitor cell proliferation, Sigma-Aldrich Dmd antibody (Sigma-Aldrich, D-8043) was used in immunohistochemistry on human samples at 1:100 (fig 2 A-i). J Appl Physiol (1985) (2015) ncbi
mouse monoclonal (MANDRA1)
  • immunoprecipitation; rat; fig s3
  • immunocytochemistry; rat; 1:500; fig 7
  • western blot; rat; 1:500; fig s2
Sigma-Aldrich Dmd antibody (Sigma, Mandra-1) was used in immunoprecipitation on rat samples (fig s3), in immunocytochemistry on rat samples at 1:500 (fig 7) and in western blot on rat samples at 1:500 (fig s2). PLoS ONE (2015) ncbi
mouse monoclonal (MANDYS8)
  • immunohistochemistry - frozen section; human
Sigma-Aldrich Dmd antibody (Sigma-Aldrich, D8168) was used in immunohistochemistry - frozen section on human samples . Muscle Nerve (2015) ncbi
mouse monoclonal (MANDYS8)
  • western blot knockout validation; human; 1:1000; fig 5D
Sigma-Aldrich Dmd antibody (Sigma, D8168) was used in western blot knockout validation on human samples at 1:1000 (fig 5D). Nat Commun (2015) ncbi
mouse monoclonal (MANDYS8)
  • western blot; human; 1:1000
Sigma-Aldrich Dmd antibody (Sigma, MANDYS8) was used in western blot on human samples at 1:1000. Mol Ther (2015) ncbi
mouse monoclonal (MANDYS8)
  • immunohistochemistry; mouse; 1:100
Sigma-Aldrich Dmd antibody (Sigma, D8168) was used in immunohistochemistry on mouse samples at 1:100. PLoS ONE (2014) ncbi
Articles Reviewed
  1. Panduro M, Benoist C, Mathis D. Treg cells limit IFN-? production to control macrophage accrual and phenotype during skeletal muscle regeneration. Proc Natl Acad Sci U S A. 2018;115:E2585-E2593 pubmed publisher
  2. Long C, Li H, Tiburcy M, Rodriguez Caycedo C, Kyrychenko V, Zhou H, et al. Correction of diverse muscular dystrophy mutations in human engineered heart muscle by single-site genome editing. Sci Adv. 2018;4:eaap9004 pubmed publisher
  3. Vanhoutte D, Schips T, Kwong J, Davis J, Tjondrokoesoemo A, Brody M, et al. Thrombospondin expression in myofibers stabilizes muscle membranes. elife. 2016;5: pubmed publisher
  4. Ryan T, Schmidt C, Green T, Spangenburg E, Neufer P, McClung J. Targeted Expression of Catalase to Mitochondria Protects Against Ischemic Myopathy in High-Fat Diet-Fed Mice. Diabetes. 2016;65:2553-68 pubmed publisher
  5. Park S, Yun Y, Lim J, Kim M, Kim S, Kim J, et al. Stabilin-2 modulates the efficiency of myoblast fusion during myogenic differentiation and muscle regeneration. Nat Commun. 2016;7:10871 pubmed publisher
  6. Strauss J, Shaw C, Bradley H, Wilson O, Dorval T, Pilling J, et al. Immunofluorescence microscopy of SNAP23 in human skeletal muscle reveals colocalization with plasma membrane, lipid droplets, and mitochondria. Physiol Rep. 2016;4: pubmed publisher
  7. Nelson C, Hakim C, Ousterout D, Thakore P, Moreb E, Castellanos Rivera R, et al. In vivo genome editing improves muscle function in a mouse model of Duchenne muscular dystrophy. Science. 2016;351:403-7 pubmed publisher
  8. Long C, Amoasii L, Mireault A, McAnally J, Li H, Sanchez Ortiz E, et al. Postnatal genome editing partially restores dystrophin expression in a mouse model of muscular dystrophy. Science. 2016;351:400-3 pubmed publisher
  9. Farup J, De Lisio M, Rahbek S, Bjerre J, Vendelbo M, Boppart M, et al. Pericyte response to contraction mode-specific resistance exercise training in human skeletal muscle. J Appl Physiol (1985). 2015;119:1053-63 pubmed publisher
  10. Rodríguez Muñoz R, Cárdenas Aguayo M, Alemán V, Osorio B, Chávez González O, Rendon A, et al. Novel Nuclear Protein Complexes of Dystrophin 71 Isoforms in Rat Cultured Hippocampal GABAergic and Glutamatergic Neurons. PLoS ONE. 2015;10:e0137328 pubmed publisher
  11. Vulin A, Wein N, Simmons T, Rutherford A, Findlay A, Yurkoski J, et al. The first exon duplication mouse model of Duchenne muscular dystrophy: A tool for therapeutic development. Neuromuscul Disord. 2015;25:827-34 pubmed publisher
  12. Molsted S, Andersen J, Harrison A, Eidemak I, Mackey A. Fiber type-specific response of skeletal muscle satellite cells to high-intensity resistance training in dialysis patients. Muscle Nerve. 2015;52:736-45 pubmed publisher
  13. Ousterout D, Kabadi A, Thakore P, Majoros W, Reddy T, Gersbach C. Multiplex CRISPR/Cas9-based genome editing for correction of dystrophin mutations that cause Duchenne muscular dystrophy. Nat Commun. 2015;6:6244 pubmed publisher
  14. Ousterout D, Kabadi A, Thakore P, Perez Pinera P, Brown M, Majoros W, et al. Correction of dystrophin expression in cells from Duchenne muscular dystrophy patients through genomic excision of exon 51 by zinc finger nucleases. Mol Ther. 2015;23:523-32 pubmed publisher
  15. Gouspillou G, Sgarioto N, Norris B, Barbat Artigas S, Aubertin Leheudre M, Morais J, et al. The relationship between muscle fiber type-specific PGC-1α content and mitochondrial content varies between rodent models and humans. PLoS ONE. 2014;9:e103044 pubmed publisher
  16. Pratt S, Shah S, Ward C, Kerr J, Stains J, Lovering R. Recovery of altered neuromuscular junction morphology and muscle function in mdx mice after injury. Cell Mol Life Sci. 2015;72:153-64 pubmed publisher
  17. Randazzo D, Giacomello E, Lorenzini S, Rossi D, Pierantozzi E, Blaauw B, et al. Obscurin is required for ankyrinB-dependent dystrophin localization and sarcolemma integrity. J Cell Biol. 2013;200:523-36 pubmed publisher