SGCA monoclonal antibody, clone ABGE-19

Catalog # MAB19543

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Size:100 uL
Price: USD $ 428.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

Western blot analysis of human skeletal muscle lysate with SGCA monoclonal antibody.

  • 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 analysis of human skeletal muscle lysate with SGCA monoclonal antibody.

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)

    Immunoprecipitation

  • Gene Info — SGCA

    Entrez GeneID

    6442

    Protein Accession#

    Q16586

    Gene Name

    SGCA

    Gene Alias

    50-DAG, A2, ADL, DAG2, DMDA2, LGMD2D, SCARMD1, adhalin

    Gene Description

    sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)

    Omim ID

    600119 608099

    Gene Ontology

    Hyperlink

    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

  • Interactome
  • Pathway
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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