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DOK7 antibody

This Mouse Monoclonal antibody specifically detects DOK7 in WB and FACS. It exhibits reactivity toward Human.
Catalog No. ABIN2719664

Quick Overview for DOK7 antibody (ABIN2719664)

Target

See all DOK7 Antibodies
DOK7 (Docking Protein 7 (DOK7))

Reactivity

  • 31
  • 22
  • 18
Human

Host

  • 45
  • 4
  • 1
  • 1
Mouse

Clonality

  • 47
  • 4
Monoclonal

Conjugate

  • 20
  • 4
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This DOK7 antibody is un-conjugated

Application

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

Clone

3C12
  • Characteristics

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

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

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

    Isotype

    IgG2b
  • Application Notes

    WB 1:2000, FLOW 1:100,

    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

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

    Preservative

    Sodium azide

    Precaution of Use

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C
  • Target

    DOK7 (Docking Protein 7 (DOK7))

    Alternative Name

    DOK7

    Background

    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.

    Molecular Weight

    52.9 kDa

    Gene ID

    285489

    NCBI Accession

    NM_173660

    HGNC

    285489

    Pathways

    Skeletal Muscle Fiber Development
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