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Myosin VI antibody (C-Term)

This Rabbit Polyclonal antibody specifically detects Myosin VI in WB, IF and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN655513

Quick Overview for Myosin VI antibody (C-Term) (ABIN655513)

Target

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

Reactivity

  • 19
  • 18
  • 18
  • 2
  • 1
Human

Host

  • 32
  • 1
Rabbit

Clonality

  • 32
  • 1
Polyclonal

Conjugate

  • 14
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  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Myosin VI antibody is un-conjugated

Application

  • 18
  • 17
  • 13
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  • 1
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Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB19127
  • Binding Specificity

    • 15
    • 7
    • 4
    • 2
    • 2
    • 1
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    • 1
    AA 1166-1195, C-Term

    Predicted Reactivity

    B, M

    Purification

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

    Immunogen

    This MYO6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1166-1195 amino acids from the C-terminal region of human MYO6.

    Isotype

    Ig Fraction
  • Application Notes

    IF: 1:10~50. WB: 1:2000-1:8000. IHC-P: 1:50~100

    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

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    Myosin VI (MYO6)

    Alternative Name

    MYO6

    Background

    This gene encodes a protein involved intracellular vesicle and organelle transport, especially in the hair cell of the inner ear. Mutations in this gene have been found in patients with non-syndromic autosomal dominant and recessive hearing loss.

    Molecular Weight

    149691

    Gene ID

    4646

    NCBI Accession

    NP_004990

    UniProt

    Q9UM54

    Pathways

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