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DOK7 antibody (N-Term)

The Rabbit Polyclonal anti-DOK7 antibody has been validated for WB. It is suitable to detect DOK7 in samples from Mouse.
Catalog No. ABIN657491

Quick Overview for DOK7 antibody (N-Term) (ABIN657491)

Target

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

Reactivity

  • 32
  • 22
  • 18
Mouse

Host

  • 45
  • 4
  • 1
  • 1
Rabbit

Clonality

  • 47
  • 4
Polyclonal

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
  • 19
  • 13
  • 13
  • 10
  • 7
  • 7
  • 4
  • 4
  • 3
  • 2
Western Blotting (WB)

Clone

RB32528
  • Binding Specificity

    • 15
    • 7
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 26-55, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This DOK7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 26-55 amino acids from the N-terminal region of human DOK7.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    DOK7 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Expiry Date

    6 months
  • 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

    53097

    Gene ID

    285489

    NCBI Accession

    NP_001158145, NP_001243825, NP_775931

    UniProt

    Q18PE1

    Pathways

    Skeletal Muscle Fiber Development
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