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DOK7 Antikörper

Dieses Maus Monoklonal-Antikörper erkennt spezifisch DOK7 in WB und FACS. Er zeigt eine Reaktivität gegenüber Human.
Produktnummer ABIN2719664

Kurzübersicht für DOK7 Antikörper (ABIN2719664)

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), Flow Cytometry (FACS)

Klon

3C12
  • 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

    IgG2b
  • Applikationshinweise

    WB 1:2000, 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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