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Myosin 9 antibody

This Rabbit Polyclonal antibody specifically detects Myosin 9 in WB, ELISA and IHC. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN7116598

Quick Overview for Myosin 9 antibody (ABIN7116598)

Target

See all Myosin 9 (MYH9) Antibodies
Myosin 9 (MYH9)

Reactivity

  • 66
  • 13
  • 11
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 52
  • 12
  • 2
  • 1
  • 1
Rabbit

Clonality

  • 52
  • 16
Polyclonal

Conjugate

  • 42
  • 5
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Myosin 9 antibody is un-conjugated

Application

  • 47
  • 37
  • 18
  • 14
  • 11
  • 10
  • 9
  • 8
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
  • Purification

    Immunogen affinity purified

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    myosin, heavy chain 9, non-muscle

    Isotype

    IgG
  • Application Notes

    WB: 1:1000 - 1:2000, IHC: 1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 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

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Expiry Date

    12 months
  • Target

    Myosin 9 (MYH9)

    Alternative Name

    MYH9

    Background

    Synonyms:BDPLT6 Background:This gene encodes a conventional non-muscle myosin, this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.

    Molecular Weight

    250 kDa

    Gene ID

    4627

    UniProt

    P35579

    Pathways

    Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
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