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USH1G antibody

USH1G Reactivity: Human ELISA, IP Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7120659
  • Target See all USH1G Antibodies
    USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
    Reactivity
    • 7
    • 1
    Human
    Host
    • 7
    Rabbit
    Clonality
    • 7
    Polyclonal
    Conjugate
    • 3
    • 2
    • 1
    • 1
    This USH1G antibody is un-conjugated
    Application
    • 5
    • 2
    • 1
    • 1
    • 1
    ELISA, Immunoprecipitation (IP)
    Purification
    Immunogen affinity purified
    Purity
    ≥95 % as determined by SDS-PAGE
    Immunogen
    Usher syndrome 1G(autosomal recessive)
    Isotype
    IgG
    Top Product
    Discover our top product USH1G Primary Antibody
  • Application Notes
    IP: 1:200-1:2000
    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
    USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
    Alternative Name
    USH1G (USH1G Products)
    Synonyms
    ANKS4A antibody, SANS antibody, Sans antibody, js antibody, USH1 protein network component sans antibody, USH1G antibody, Ush1g antibody
    Background
    Synonyms:ANKS4A, FLJ33924, SANS, USH1G, Usher syndrome type 1G protein Background:Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.
    Molecular Weight
    52 kDa
    Gene ID
    124590
    UniProt
    Q495M9
    Pathways
    Sensory Perception of Sound
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