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Characterizing Exon Skipping Efficiency in DMD Patient Samples in Clinical Trials of Antisense Oligonucleotides
Journal JoVE
Médecine
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Journal JoVE Médecine
Characterizing Exon Skipping Efficiency in DMD Patient Samples in Clinical Trials of Antisense Oligonucleotides

Characterizing Exon Skipping Efficiency in DMD Patient Samples in Clinical Trials of Antisense Oligonucleotides

DOI:
10.3791/60672-v

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05:16 min

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May 07, 2020

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, , , , ,
1Department of Molecular Therapy, National Institute of Neuroscience,National Center of Neurology and Psychiatry, 2Clinical Research Support Office, Translational Medical Center,National Center of Neurology and Psychiatry, 3Department of Child Neurology, National Center Hospital,National Center of Neurology and Psychiatry

Chapitres

  • 00:04Introduction
  • 01:05Muscle Sample Preparation
  • 02:10Muscle Sectioning
  • 03:00Results: Representative Exon Skipping Efficiency and Dystrophin Quantification
  • 04:23Conclusion

Summary

Traduction automatique

Traduction automatique

Here, we present the molecular characterization of dystrophin 38 expression using Sanger sequencing, RT-PCR, and western blotting in the clinical trial.

Tags

Exon SkippingDMDAntisense OligonucleotidesClinical TrialsSample PreparationCryostat SectioningRT-PCRWestern BlotImmunohistochemistryHematoxylin And Eosin StainingMicrochip ElectrophoresisSequencing

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