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DAG1 antibody

GTX105038
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
TargetDAG1
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Overview

  • Supplier
    GeneTex
  • Product Name
    DAG1 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1.28 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID1605
  • Target name
    DAG1
  • Target description
    dystroglycan 1
  • Target synonyms
    156DAG, A3a, AGRNR, DAG, LGMDR16, MDDGA9, MDDGC7, MDDGC9, dystroglycan 1, dystroglycan 1 (dystrophin-associated glycoprotein 1)
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ14118
  • Protein Name
    Dystroglycan 1
  • Scientific Description
    Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. [provided by RefSeq]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

References

  • Riemersma M, Mandel H, van Beusekom E, et al. Absence of α- and β-dystroglycan is associated with Walker-Warburg syndrome. Neurology. 2015,84(21):2177-82. doi: 10.1212/WNL.0000000000001615
    Read this paper
  • Riemersma M, Sandrock J, Boltje TJ, et al. Disease mutations in CMP-sialic acid transporter SLC35A1 result in abnormal α-dystroglycan O-mannosylation, independent from sialic acid. Hum Mol Genet. 2015,24(8):2241-6. doi: 10.1093/hmg/ddu742
    Read this paper
  • Donadeu FX, Fahiminiya S, Esteves CL, et al. Transcriptome profiling of granulosa and theca cells during dominant follicle development in the horse. Biol Reprod. 2014,91(5):111. doi: 10.1095/biolreprod.114.118943
    Read this paper
  • Jae LT, Raaben M, Herbert AS, et al. Virus entry. Lassa virus entry requires a trigger-induced receptor switch. Science. 2014,344(6191):1506-10. doi: 10.1126/science.1252480
    Read this paper