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Arhgef9 antibody

Arhgef9 Reactivity: Human, Rat, Mouse ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN2422657
  • Target See all Arhgef9 Antibodies
    Arhgef9 (Cdc42 Guanine Nucleotide Exchange Factor (GEF) 9 (Arhgef9))
    Reactivity
    • 35
    • 11
    • 7
    • 1
    Human, Rat, Mouse
    Host
    • 34
    • 4
    Rabbit
    Clonality
    • 33
    • 4
    Polyclonal
    Conjugate
    • 21
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Arhgef9 antibody is un-conjugated
    Application
    • 24
    • 21
    • 21
    • 5
    • 1
    • 1
    • 1
    • 1
    ELISA, Immunohistochemistry (IHC)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human ARHGEF9
    Isotype
    IgG
    Top Product
    Discover our top product Arhgef9 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.3 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Handling Advice
    Avoid freeze / thaw cycles.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    Arhgef9 (Cdc42 Guanine Nucleotide Exchange Factor (GEF) 9 (Arhgef9))
    Alternative Name
    ARHGEF9 (Arhgef9 Products)
    Synonyms
    arhgef9 antibody, wu:fj33b10 antibody, COLLYBISTIN antibody, EIEE8 antibody, HPEM-2 antibody, PEM-2 antibody, PEM2 antibody, 9630036L12Rik antibody, A230067K14 antibody, mKIAA0424 antibody, ARHGEF9 antibody, Cdc42 guanine nucleotide exchange factor 9 antibody, Cdc42 guanine nucleotide exchange factor (GEF) 9b antibody, Cdc42 guanine nucleotide exchange factor (GEF) 9 antibody, CDC42 guanine nucleotide exchange factor (GEF) 9 antibody, ARHGEF9 antibody, arhgef9b antibody, arhgef9 antibody, Arhgef9 antibody
    Background
    The protein encoded by this gene is a Rho-like GTPase that switches between the active (GTP-bound) state and inactive (GDP-bound) state to regulate CDC42 and other genes. Defects in this gene are a cause of startle disease with epilepsy (STHEE), also known as hyperekplexia with epilepsy. Three transcript variants encoding different isoforms have been found for this gene.
    Pathways
    Neurotrophin Signaling Pathway
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