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Myosin VIIA antibody (AA 850-1150)

The Rabbit Polyclonal anti-Myosin VIIA antibody has been validated for WB. It is suitable to detect Myosin VIIA in samples from Human.
Catalog No. ABIN6144293

Quick Overview for Myosin VIIA antibody (AA 850-1150) (ABIN6144293)

Target

See all Myosin VIIA (MYO7A) Antibodies
Myosin VIIA (MYO7A)

Reactivity

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Human

Host

  • 38
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Rabbit

Clonality

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Polyclonal

Conjugate

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This Myosin VIIA antibody is un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 850-1150

    Sequence

    MIARRLHQRL RAEYLWRLEA EKMRLAEEEK LRKEMSAKKA KEEAERKHQE RLAQLAREDA ERELKEKEAA RRKKELLEQM ERARHEPVNH SDMVDKMFGF LGTSGGLPGQ EGQAPSGFED LERGRREMVE EDLDAALPLP DEDEEDLSEY KFAKFAATYF QGTTTHSYTR RPLKQPLLYH DDEGDQLAAL AVWITILRFM GDLPEPKYHT AMSDGSEKIP VMTKIYETLG KKTYKRELQA LQGEGEAQLP EGQKKSSVRH KLVHLTLKKK SKLTEEVTKR LHDGESTVQG NSMLEDRPTS N

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 850-1150 of human MYO7A (NP_000251.3).

    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 VIIA (MYO7A)

    Alternative Name

    MYO7A

    Background

    This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.,MYO7A,DFNA11,DFNB2,MYOVIIA,MYU7A,NSRD2,USH1B,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,MYO7A

    Molecular Weight

    138 kDa/240 kDa/249 kDa/250 kDa/254 kDa

    Gene ID

    4647

    UniProt

    Q13402

    Pathways

    Sensory Perception of Sound
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