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SGCA monoclonal antibody, clone ABGE-19  

  • Catalog # : MAB19543
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against synthetic peptide of human SGCA.
  • Immunogen:
  • A synthetic peptide corresponding to human SGCA.
  • Host:
  • Rabbit
  • Reactivity:
  • Human, Mouse, Rat
  • Form:
  • Liquid
  • Purification:
  • Affinity purification
  • Isotype:
  • IgG
  • Recommend Usage:
  • Immunohistochemistry (1:100-1:500)
    Immunoprecipitation (1:40)
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
  • Storage Instruction:
  • Store at -20°C for one year. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for a longer time. Avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • Western blot analysis of human skeletal muscle lysate with SGCA monoclonal antibody.
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunoprecipitation
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunoprecipitation
  • Gene Information
  • Entrez GeneID:
  • 6442
  • Gene Name:
  • SGCA
  • Gene Alias:
  • 50-DAG,A2,ADL,DAG2,DMDA2,LGMD2D,SCARMD1,adhalin
  • Gene Description:
  • sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
  • Gene Summary:
  • This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq
  • Other Designations:
  • 50kD DAG,sarcoglycan, alpha
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