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Myosin 9 antibody

This anti-Myosin 9 antibody is a Rabbit Polyclonal antibody detecting Myosin 9 in WB, ELISA, IHC, IF and IP. Suitable for Human, Mouse, Rat and Zebrafish (Danio rerio).
Catalog No. ABIN5701128

Quick Overview for Myosin 9 antibody (ABIN5701128)

Target

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

Reactivity

  • 66
  • 13
  • 10
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat, Zebrafish (Danio rerio)

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
  • 13
  • 11
  • 9
  • 9
  • 8
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)
  • Immunogen

    myosin, heavy chain 9, non-muscle

    Isotype

    IgG
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    mouse kidney tissue were subjected to SDS PAGE followed by western blot with FNab05479(MYH9 antibody) at dilution of 1:1000

    Restrictions

    For Research Use only
  • 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.

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    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

    224 kDa

    Gene ID

    4627

    UniProt

    P35579

    Pathways

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