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Myosin 9 antibody (pSer1943)

The Rabbit Polyclonal anti-Myosin 9 antibody has been validated for WB. It is suitable to detect Myosin 9 in samples from Human.
Catalog No. ABIN7268744

Quick Overview for Myosin 9 antibody (pSer1943) (ABIN7268744)

Target

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

Reactivity

  • 64
  • 14
  • 11
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 50
  • 12
  • 2
  • 1
  • 1
Rabbit

Clonality

  • 50
  • 16
Polyclonal

Conjugate

  • 40
  • 5
  • 5
  • 5
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Myosin 9 antibody is un-conjugated

Application

  • 46
  • 37
  • 17
  • 13
  • 11
  • 9
  • 9
  • 7
  • 2
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 8
    • 7
    • 5
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    pSer1943

    Purpose

    Phospho-MYH9-S1943 Rabbit pAb

    Sequence

    DGSDE

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Phosphorylated Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthetic phosphorylated peptide around S1943 of human MYH9 (NP_002464.1).

    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 9 (MYH9)

    Alternative Name

    MYH9

    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.,MYH9,BDPLT6,DFNA17,EPSTS,FTNS,MHA,NMHC-II-A,NMMHC-IIA,NMMHCA,myosin-9,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,Protein phosphorylation,MYH9

    Molecular Weight

    159kDa/226kDa

    Gene ID

    4627

    UniProt

    P35579

    Pathways

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