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TMIE antibody (Middle Region)

This Rabbit Polyclonal antibody specifically detects TMIE in WB and EIA. It exhibits reactivity toward Human.
Catalog No. ABIN955258

Quick Overview for TMIE antibody (Middle Region) (ABIN955258)

Target

See all TMIE Antibodies
TMIE (Transmembrane Inner Ear (TMIE))

Reactivity

  • 10
  • 2
Human

Host

  • 9
  • 1
Rabbit

Clonality

  • 10
Polyclonal

Conjugate

  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
This TMIE antibody is un-conjugated

Application

Western Blotting (WB), Enzyme Immunoassay (EIA)
  • Binding Specificity

    • 7
    • 1
    • 1
    • 1
    • 1
    AA 78-108, Middle Region

    Specificity

    This antibody detects TMIE (Center).

    Cross-Reactivity (Details)

    Species reactivity (tested):Human

    Purification

    Protein A column followed by peptide affinity purification

    Immunogen

    KLH conjugated synthetic peptide between 78~108 amino acids from the Central region of human TMIE

    Isotype

    Ig Fraction
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.25 mg/mL

    Buffer

    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.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.
  • Target

    TMIE (Transmembrane Inner Ear (TMIE))

    Alternative Name

    TMIE

    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.Synonyms: Transmembrane inner ear expressed protein

    Gene ID

    259236

    NCBI Accession

    NP_671729

    Pathways

    Sensory Perception of Sound
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