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TMIE antibody (AA 71-100)

The Rabbit Polyclonal anti-TMIE antibody has been validated for WB. It is suitable to detect TMIE in samples from Human and Mouse.
Catalog No. ABIN653717

Quick Overview for TMIE antibody (AA 71-100) (ABIN653717)

Target

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

Reactivity

Human, Mouse

Host

  • 9
  • 1
Rabbit

Clonality

  • 10
Polyclonal

Conjugate

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

Application

  • 9
  • 9
  • 1
Western Blotting (WB)

Clone

RB24522
  • Binding Specificity

    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 71-100

    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.

    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

    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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