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Myosin VI antibody (AA 1016-1285)

This anti-Myosin VI antibody is a Rabbit Polyclonal antibody detecting Myosin VI in WB. Suitable for Human.
Catalog No. ABIN6144291

Quick Overview for Myosin VI antibody (AA 1016-1285) (ABIN6144291)

Target

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

Reactivity

  • 19
  • 18
  • 18
  • 2
  • 1
Human

Host

  • 32
  • 1
Rabbit

Clonality

  • 32
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Polyclonal

Conjugate

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  • 1
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This Myosin VI antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

    • 15
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    • 1
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    AA 1016-1285

    Sequence

    IAQSEAELIS DEAQADLALR RNDGTRPKMT PEQMAKEMSE FLSRGPAVLA TKAAAGTKKY DLSKWKYAEL RDTINTSCDI ELLAACREEF HRRLKVYHAW KSKNKKRNTE TEQRAPKSVT DYDFAPFLNN SPQQNPAAQI PARQREIEMN RQQRFFRIPF IRPADQYKDP QSKKKGWWYA HFDGPWIARQ MELHPDKPPI LLVAGKDDME MCELNLEETG LTRKRGAEIL PRQFEEIWER CGGIQYLQNA IESRQARPTY ATAMLQSLLK

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1016-1285 of human MYO6 (NP_004990.3).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Myosin VI (MYO6)

    Alternative Name

    MYO6

    Background

    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.,MYO6,DFNA22,DFNB37,Myo6-007,Myo6-008,myosin VI,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,MYO6

    Molecular Weight

    145 kDa/146 kDa/148 kDa/149 kDa

    Gene ID

    4646

    UniProt

    Q9UM54

    Pathways

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