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Last updated: 2022/5/22

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SGCG monoclonal antibody, clone AbS34 

  • Catalog # : MAB20069
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against synthetic peptide of human SGCG.
  • Immunogen:
  • A synthetic peptide corresponding to human SGCG.
  • Host:
  • Rabbit
  • Theoretical MW (kDa):
  • 32.379
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Affinity purification
  • Isotype:
  • IgG
  • Recommend Usage:
  • Immunohistochemistry (1:50-1:200)
    Immunoprecipitation (1:50)
    Western Blot (1:500-1:2000)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, 150 mM NaCl, pH 7.4 (50% glycerol, 0.02% sodium azide).
  • 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 tissue lysate with SGCG monoclonal antibody, clone AbS34 (Cat # MAB20069).
  • Immunohistochemistry
  • Immunoprecipitation
  • Application Image
  • Western Blot (Cell lysate)
  • Western Blot (Cell lysate)
  • enlarge
  • Immunohistochemistry
  • Immunoprecipitation
  • Gene Information
  • Entrez GeneID:
  • 6445
  • Gene Name:
  • SGCG
  • Gene Alias:
  • A4,DAGA4,DMDA,DMDA1,LGMD2C,MAM,MGC130048,SCARMD2,SCG3,TYPE
  • Gene Description:
  • sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
  • Gene Summary:
  • This gene encodes gamma-sarcoglycan, one of several sarcolemmal transmembrane glycoproteins that interact with dystrophin. The dystrophin-glycoprotein complex (DGC) spans the sarcolemma and is comprised of dystrophin, syntrophin, alpha- and beta-dystroglycans and sarcoglycans. The DGC provides a structural link between the subsarcolemmal cytoskeleton and the extracellular matrix of muscle cells. Defects in the encoded protein can lead to early onset autosomal recessive muscular dystrophy, in particular limb-girdle muscular dystrophy, type 2C (LGMD2C). [provided by RefSeq
  • Other Designations:
  • 35kD dystrophin-associated glycoprotein,OTTHUMP00000018112,gamma sarcoglycan,sarcoglycan, gamma (35kD dystrophin-associated glycoprotein)
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