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MYO5A antibody (AA 950-1150)

The Rabbit Polyclonal anti-MYO5A antibody has been validated for WB and IF. It is suitable to detect MYO5A in samples from Human.
Catalog No. ABIN6144285

Quick Overview for MYO5A antibody (AA 950-1150) (ABIN6144285)

Target

See all MYO5A Antibodies
MYO5A (Myosin VA (MYO5A))

Reactivity

  • 21
  • 8
  • 5
Human

Host

  • 21
  • 1
Rabbit

Clonality

  • 22
Polyclonal

Conjugate

  • 12
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MYO5A antibody is un-conjugated

Application

  • 12
  • 11
  • 5
  • 3
  • 3
  • 2
Western Blotting (WB), Immunofluorescence (IF)
  • Binding Specificity

    • 6
    • 5
    • 1
    • 1
    • 1
    • 1
    AA 950-1150

    Sequence

    LTNLEGIYNS ETEKLRSDLE RLQLSEEEAK VATGRVLSLQ EEIAKLRKDL EQTRSEKKCI EEHADRYKQE TEQLVSNLKE ENTLLKQEKE ALNHRIVQQA KEMTETMEKK LVEETKQLEL DLNDERLRYQ NLLNEFSRLE ERYDDLKEEM TLMVHVPKPG HKRTDSTHSS NESEYIFSSE IAEMEDIPSR TEEPSEKKVP L

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 950-1150 of human MYO5A (NP_000250.3).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:100

    Comment

    HIGH QUALITY

    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

    MYO5A (Myosin VA (MYO5A))

    Alternative Name

    MYO5A

    Background

    This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined.,MYO5A,GS1,MYH12,MYO5,MYR12,myosin VA,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,Endocrine & Metabolism,Mitochondrial metabolism,Neuroscience,MYO5A

    Molecular Weight

    212 kDa/215 kDa/218 kDa

    Gene ID

    4644

    UniProt

    Q9Y4I1

    Pathways

    Hormone Transport, Peptide Hormone Metabolism
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