Recombinant Anti-Dysferlin antibody [JAI-1-49-3] (ab124684)

Publishing research using ab124684? Please let us know so that we can cite the reference in this datasheet.

ab124684 has been referenced in 22 publications.

  • Xu S  et al. Improved efficacy of a next-generation ERT in murine Pompe disease. JCI Insight 4:N/A (2019). PubMed: 30843882
  • Dominov JA  et al. Correction of pseudoexon splicing caused by a novel intronic dysferlin mutation. Ann Clin Transl Neurol 6:642-654 (2019). PubMed: 31019989
  • Malcher J  et al. Exon Skipping in a Dysf-Missense Mutant Mouse Model. Mol Ther Nucleic Acids 13:198-207 (2018). PubMed: 30292141
  • Lynch JM  et al. Mutant myocilin impacts sarcomere ultrastructure in mouse gastrocnemius muscle. PLoS One 13:e0206801 (2018). PubMed: 30395621
  • Piper AK  et al. Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling. Cell Signal 33:30-40 (2017). PubMed: 28192161
  • Llanga T  et al. Structure-Based Designed Nano-Dysferlin Significantly Improves Dysferlinopathy in BLA/J Mice. Mol Ther 25:2150-2162 (2017). PubMed: 28629822
  • Woolger N  et al. Limited proteolysis as a tool to probe the tertiary conformation of dysferlin and structural consequences of patient missense variant L344P. J Biol Chem 292:18577-18591 (2017). PubMed: 28904177
  • Hofhuis J  et al. Dysferlin mediates membrane tubulation and links T-tubule biogenesis to muscular dystrophy. J Cell Sci 130:841-852 (2017). PubMed: 28104817
  • Ma J  et al. DNA-Mediated Gene Therapy in a Mouse Model of Limb Girdle Muscular Dystrophy 2B. Mol Ther Methods Clin Dev 7:123-131 (2017). WB . PubMed: 29159199
  • Sabha N  et al. PIK3C2B inhibition improves function and prolongs survival in myotubular myopathy animal models. J Clin Invest 126:3613-25 (2016). PubMed: 27548528
  • Escobar H  et al. Full-length Dysferlin Transfer by the Hyperactive Sleeping Beauty Transposase Restores Dysferlin-deficient Muscle. Mol Ther Nucleic Acids 5:e277 (2016). PubMed: 26784637
  • Vanhoutte D  et al. Thrombospondin expression in myofibers stabilizes muscle membranes. Elife 5:N/A (2016). WB ; Mouse . PubMed: 27669143
  • Bhattacharyya S  et al. Endocytic recycling protein EHD1 regulates primary cilia morphogenesis and SHH signaling during neural tube development. Sci Rep 6:20727 (2016). PubMed: 26884322
  • Hammers DW  et al. Disease-modifying effects of orally bioavailable NF-?B inhibitors in dystrophin-deficient muscle. JCI Insight 1:e90341 (2016). PubMed: 28018975
  • Pryadkina M  et al. A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2?kb Dysferlin coding sequence. Mol Ther Methods Clin Dev 2:15009 (2015). IHC . PubMed: 26029720
  • Tzeng HP  et al. Dysferlin mediates the cytoprotective effects of TRAF2 following myocardial ischemia reperfusion injury. J Am Heart Assoc 3:e000662 (2014). WB ; Mouse . PubMed: 24572254
  • Defour A  et al. Dysferlin regulates cell membrane repair by facilitating injury-triggered acid sphingomyelinase secretion. Cell Death Dis 5:e1306 (2014). ICC/IF ; Human . PubMed: 24967968
  • Kim SC  et al. TRIM72 is required for effective repair of alveolar epithelial cell wounding. Am J Physiol Lung Cell Mol Physiol 307:L449-59 (2014). PubMed: 25106429
  • Lek A  et al. Calpains, cleaved mini-dysferlinC72, and L-type channels underpin calcium-dependent muscle membrane repair. J Neurosci 33:5085-94 (2013). WB ; Human . PubMed: 23516275
  • Kerr JP  et al. Dysferlin stabilizes stress-induced Ca2+ signaling in the transverse tubule membrane. Proc Natl Acad Sci U S A 110:20831-6 (2013). ICC/IF ; Mouse . PubMed: 24302765
  • Azakir BA  et al. Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells. J Biol Chem 287:10344-54 (2012). PubMed: 22318734
  • Wang ZQ  et al. Distinguishing the 4qA and 4qB variants is essential for the diagnosis of facioscapulohumeral muscular dystrophy in the Chinese population. Eur J Hum Genet 19:64-9 (2011). WB ; Human . PubMed: 20736973

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