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DOK7 Antikörper

Dieser Maus Monoklonal Antikörper erkennt spezifisch DOK7 in WB, IHC und FACS. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN2719663

Kurzübersicht für DOK7 Antikörper (ABIN2719663)

Target

Alle DOK7 Antikörper anzeigen
DOK7 (Docking Protein 7 (DOK7))

Reaktivität

  • 31
  • 22
  • 18
Human

Wirt

  • 45
  • 4
  • 1
  • 1
Maus

Klonalität

  • 47
  • 4
Monoklonal

Konjugat

  • 20
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser DOK7 Antikörper ist unkonjugiert

Applikation

  • 40
  • 18
  • 13
  • 13
  • 10
  • 6
  • 6
  • 4
  • 4
  • 3
  • 2
Western Blotting (WB), Immunohistochemistry (IHC), Flow Cytometry (FACS)

Klon

1D11
  • Produktmerkmale

    Homo sapiens docking protein 7 (DOK7), transcript variant 1

    Aufreinigung

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Full length human recombinant protein of human DOK7(NP_775931) produced in HEK293T cell.

    Isotyp

    IgG2a
  • Applikationshinweise

    WB 1:2000, IHC 1:150, FLOW 1:100,

    Kommentare

    The concentration of the product may vary between diferrent lots.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % sodium azide.

    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
  • Target

    DOK7 (Docking Protein 7 (DOK7))

    Andere Bezeichnung

    DOK7

    Hintergrund

    The protein encoded by this gene is essential for neuromuscular synaptogenesis. The protein functions in aneural activation of muscle-specific receptor kinase, which is required for postsynaptic differentiation, and in the subsequent clustering of the acetylcholine receptor in myotubes. This protein can also induce autophosphorylation of muscle-specific receptor kinase. Mutations in this gene are a cause of familial limb-girdle myasthenia autosomal recessive, which is also known as congenital myasthenic syndrome type 1B. Alternative splicing results in multiple transcript variants.

    Molekulargewicht

    52.9 kDa

    Gen-ID

    285489

    NCBI Accession

    NM_173660

    HGNC

    285489

    Pathways

    Skeletal Muscle Fiber Development
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