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Myosin VI antibody (AA 383-786)

The Rabbit Polyclonal anti-Myosin VI antibody (ABIN7874533) specifically detects Myosin VI in WB, ELISA and FACS. The antibody is reactive with Human and Mouse samples.
Catalog No. ABIN7874533
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for Myosin VI antibody (AA 383-786) (ABIN7874533)

Target

See all Myosin VI (MYO6) Antibodies
Myosin VI (MYO6)

Reactivity

  • 19
  • 19
  • 18
  • 2
  • 1
Human, Mouse

Host

  • 32
  • 2
Rabbit

Clonality

  • 32
  • 2
Polyclonal

Conjugate

  • 15
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Myosin VI antibody is un-conjugated

Application

  • 19
  • 17
  • 13
  • 13
  • 12
  • 9
  • 7
  • 6
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • Binding Specificity

    • 15
    • 8
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 383-786

    Purpose

    MYO6 Antibody / Unconventional Myosin-6

    Purification

    Antigen affinity purified

    Immunogen

    An E.coli-derived human recombinant protein (Q383-H786) was used as the immunogen for the MYO6 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the MYO6 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the MYO6 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    Myosin VI (MYO6)

    Alternative Name

    MYO6

    Background

    Unconventional myosin-VI, is a protein that in humans is coded for by MYO6. This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

    UniProt

    Q9UM54

    Pathways

    Sensory Perception of Sound, Dicarboxylic Acid Transport, Asymmetric Protein Localization
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