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ELMOD3 antibody

ELMOD3 Reactivity: Human, Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6293242
  • Target See all ELMOD3 Antibodies
    ELMOD3 (ELMO/CED-12 Domain Containing 3 (ELMOD3))
    Reactivity
    • 13
    • 3
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 10
    • 3
    Rabbit
    Clonality
    • 13
    Polyclonal
    Conjugate
    • 9
    • 2
    • 1
    • 1
    This ELMOD3 antibody is un-conjugated
    Application
    • 9
    • 5
    • 4
    • 1
    Western Blotting (WB)
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human ELMOD3
    Isotype
    IgG
    Top Product
    Discover our top product ELMOD3 Primary Antibody
  • Application Notes
    WB 1:500 - 1:2000
    Comment

    Both isoform 1 and isoform 6 are widely expressed

    Restrictions
    For Research Use only
  • 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 -20C. Avoid freeze / thaw cycles.
  • Target
    ELMOD3 (ELMO/CED-12 Domain Containing 3 (ELMOD3))
    Alternative Name
    ELMOD3 (ELMOD3 Products)
    Synonyms
    LST3 antibody, RBED1 antibody, RBM29 antibody, AI844780 antibody, C330008I15Rik antibody, Rbed1 antibody, Kcmf1 antibody, ELMO domain containing 3 antibody, ELMO/CED-12 domain containing 3 antibody, ELMOD3 antibody, Elmod3 antibody
    Background
    This gene encodes a member of the engulfment and cell motility family of GTPase-activating proteins that regulate Arf GTPase proteins. Members of this family are defined by a conserved engulfment and cell motility domain. In rat cochlea, the encoded protein is found in stereocilia, kinocilia and cuticular plate of developing hair cells suggesting a function for this protein in cochlear sensory cells. An allelic variant of this family has been associated with autosomal recessive nonsyndromic deafness-88 in humans. Alternative splicing results in multiple transcript variants.
    Molecular Weight
    43.046 kDa
    Gene ID
    84173
    UniProt
    Q96FG2
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