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LGMD2D Foundation
  • Home
  • About Us
  • Patient Resources
  • Trials & Research
  • Donate
  • Contact Us

Current Clinical Trials

A Study of the Natural History of Patients With LGMD2E/R4, LGMD2D/R3, and LGMD2C/R5, ≥ 4 Years of Age, Who Are Managed in Routine Clinical Practice

  • Sponsor: Sarepta Therapeutics, Inc.
  • Recruitment Status: Active


Skeletal Muscle Biomarkers in People With Fragile Sarcolemmal Muscular Dystrophy

  • Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
  • Recruitment Status: Active, Not Recruiting

Past Clinical Trials

Gene Transfer Clinical Trial for LGMD2D (Alpha-sarcoglycan Deficiency) Using scAAVrh74.tMCK.hSGCA

Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)

Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)

Sponsor: Dr. Jerry R. Mendell, Nationwide Children's Hospital 


Recruitment Status: Completed

Learn more

Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)

Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)

Gene Transfer Therapy for Treating Children and Adults With Limb Girdle Muscular Dystrophy Type 2D (LGMD2D)

Sponsor: Nationwide Children's Hospital


Recruitment Status: Completed

Learn more

Research

Publications

Gene Delivery for Limb-Girdle Muscular Dystrophy Type 2D by Isolated Limb Infusion - July 2019


Sustained alpha-sarcoglycan gene expression after gene transfer in limb-girdle muscular dystrophy, type 2D - November 2010


Limb-girdle muscular dystrophy type 2D gene therapy restores alpha-sarcoglycan and associated proteins - September 2009


Early adenovirus-mediated gene transfer effectively prevents muscular dystrophy in alpha-sarcoglycan-deficient mice - August 2000


Muscular Dystrophy Association: Research on LGMD

Mouse Models

Several mouse models of sarcoglycan deficiency have been reported; two are cryopreserved at Jackson Laboratories.


B6.129S6-Sgcatm2Kcam/J (stock #008275) 

Alpha-sarcoglycan deficiency verified by western blot, RT-PCR analysis and immunofluorescence staining of skeletal muscle. Mice develop progressive muscular dystrophy as early as 6 weeks of age. 


B6.Cg-Sgcatm1KamTg(Ckm-SGCE)1Kcam/J (stock #009651) 

Homozygous for both α- and ε-sarcoglycan deficiency. These mice have no overt phenotype but have an exaggerated response to mild exercise.

DNA and RNA

DNA and RNA primers for PCR amplification

Antibodies

Abcam antibodies against alpha-sarcoglycan

  • Anti-alpha Sarcoglycan antibody [Ad1/20A6] (ab49451)
  • Anti-alpha Sarcoglycan antibody (ab92522) 
  • Anti-alpha Sarcoglycan antibody (ab130657) 

Links on Biocompare to antibodies from 16 different vendors 

Links on Antibody Resource to antibodies from 12 different vendors 

R&D Systems alpha-sarcoglycan antibody

Other resources

Bioz analyzes, aggregates, and structures data from more than 3.6 million articles and many different resources related to alpha-sarcoglycan can be found on this website.

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LGMD2D Foundation

Copyright © 2022 LGMD2D Foundation - All Rights Reserved. LGMD2D Foundation is a 501(c)(3), Est. 2013.

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