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TMIE antibody (AA 71-100)

TMIE Reactivity: Human, Mouse WB Host: Rabbit Polyclonal RB24522 unconjugated
Catalog No. ABIN653717
  • Target See all TMIE Antibodies
    TMIE (Transmembrane Inner Ear (TMIE))
    Binding Specificity
    • 7
    • 6
    • 6
    • 6
    • 1
    • 1
    AA 71-100
    Reactivity
    Human, Mouse
    Host
    • 14
    • 1
    Rabbit
    Clonality
    • 15
    Polyclonal
    Conjugate
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    This TMIE antibody is un-conjugated
    Application
    • 14
    • 14
    • 1
    Western Blotting (WB)
    Predicted Reactivity
    M
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    This TMIE antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 71-100 amino acids from the Central region of human TMIE.
    Clone
    RB24522
    Isotype
    Ig Fraction
  • Application Notes
    WB: 1:1000. WB: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    Storage Comment
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    Expiry Date
    6 months
  • Target
    TMIE (Transmembrane Inner Ear (TMIE))
    Alternative Name
    TMIE (TMIE Products)
    Synonyms
    si:ch211-163f10.1 antibody, DFNB6 antibody, 5131400L21Rik antibody, Mm.87012 antibody, sr antibody, RGD1562523 antibody, transmembrane inner ear antibody, tmie antibody, TMIE antibody, Tmie antibody
    Background
    This gene encodes a transmembrane inner ear protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory hair cells in the cochlea, including correct development of stereocilia bundles. This gene is one of multiple genes responsible for recessive non-syndromic deafness (DFNB), also known as autosomal recessive nonsyndromic hearing loss (ARNSHL), the most common form of congenitally acquired inherited hearing impairment.
    Molecular Weight
    17241
    Gene ID
    259236
    NCBI Accession
    NP_671729
    UniProt
    Q8NEW7
    Pathways
    Sensory Perception of Sound
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