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Dystrophin Antikörper

DMD Reaktivität: Human IHC, IF Wirt: Kaninchen Monoclonal unconjugated
Produktnummer ABIN7266871
  • Target Alle Dystrophin (DMD) Antikörper anzeigen
    Dystrophin (DMD)
    Reaktivität
    • 48
    • 18
    • 17
    • 5
    Human
    Wirt
    • 32
    • 17
    Kaninchen
    Klonalität
    • 26
    • 23
    Monoklonal
    Konjugat
    • 29
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    Dieser Dystrophin Antikörper ist unkonjugiert
    Applikation
    • 22
    • 19
    • 15
    • 10
    • 6
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Verwendungszweck
    Dystrophin Rabbit mAb
    Kreuzreaktivität
    Maus, Ratte
    Produktmerkmale
    Monoclonal Antibodies
    Aufreinigung
    Affinity purification
    Immunogen
    A synthesized peptide derived from human Dystrophin
    Isotyp
    IgG
    Top Product
    Discover our top product DMD Primärantikörper
  • Applikationshinweise
    IHC,1:50 - 1:200,IF,1:50 - 1:200
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Dystrophin (DMD)
    Andere Bezeichnung
    DMD (DMD Produkte)
    Hintergrund
    This gene spans a genomic range of greater than 2 Mb and encodes a large protein containing an N-terminal actin-binding domain and multiple spectrin repeats. The encoded protein forms a component of the dystrophin-glycoprotein complex (DGC), which bridges the inner cytoskeleton and the extracellular matrix. Deletions, duplications, and point mutations at this gene locus may cause Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or cardiomyopathy. Alternative promoter usage and alternative splicing result in numerous distinct transcript variants and protein isoforms for this gene. [provided by RefSeq, Dec 2016],BMD, CMD3B, DXS142, DXS164, DXS206, DXS230, DXS239, DXS268, DXS269, DXS270, DXS272, MRX85,Cell Biology & Developmental Biology,Cytoskeleton,Cytoskeleton_Microfilaments,Mesenchymal Stem Cells,Neurodegenerative Diseases,Neuroscience,Signal Transduction,Stem Cells,DMD
    Molekulargewicht
    427kDa
    Gen-ID
    1756
    UniProt
    P11532
    Pathways
    Skeletal Muscle Fiber Development
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