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TMIE anticorps (AA 71-100)

L’anticorps Lapin Polyclonal anti-TMIE a été validé pour WB. Il convient pour détecter TMIE dans des échantillons de Humain et Souris.
N° du produit ABIN653717

Aperçu rapide pour TMIE anticorps (AA 71-100) (ABIN653717)

Antigène

Voir toutes TMIE Anticorps
TMIE (Transmembrane Inner Ear (TMIE))

Reactivité

Humain, Souris

Hôte

  • 9
  • 1
Lapin

Clonalité

  • 10
Polyclonal

Conjugué

  • 5
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp TMIE est non-conjugé

Application

  • 9
  • 9
  • 1
Western Blotting (WB)

Clone

RB24522
  • Épitope

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

    Homologie

    M

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogène

    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
  • Indications d'application

    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.

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.

    Date de péremption

    6 months
  • Antigène

    TMIE (Transmembrane Inner Ear (TMIE))

    Autre désignation

    TMIE

    Sujet

    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.

    Poids moléculaire

    17241

    ID gène

    259236

    NCBI Accession

    NP_671729

    UniProt

    Q8NEW7

    Pathways

    Sensory Perception of Sound
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