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TMEM43 anticorps (AA 195-223)

L’anticorps Lapin Polyclonal anti-TMEM43 a été validé pour WB et IHC (p). Il convient pour détecter TMEM43 dans des échantillons de Humain.
N° du produit ABIN656549

Aperçu rapide pour TMEM43 anticorps (AA 195-223) (ABIN656549)

Antigène

Voir toutes TMEM43 Anticorps
TMEM43 (Transmembrane Protein 43 (TMEM43))

Reactivité

  • 19
  • 4
  • 1
Humain

Hôte

  • 19
Lapin

Clonalité

  • 17
  • 2
Polyclonal

Conjugué

  • 10
  • 3
  • 2
  • 2
  • 1
  • 1
Cet anticorp TMEM43 est non-conjugé

Application

  • 14
  • 13
  • 12
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB32139
  • Épitope

    • 6
    • 6
    • 2
    • 1
    • 1
    • 1
    AA 195-223

    Homologie

    M, Rat

    Purification

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

    Immunogène

    This TMEM43 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 195-223 amino acids from the Central region of human TMEM43.

    Isotype

    Ig Fraction
  • Indications d'application

    WB: 1:1000. IHC-P: 1:10~50

    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

    TMEM43 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.

    Date de péremption

    6 months
  • Antigène

    TMEM43 (Transmembrane Protein 43 (TMEM43))

    Autre désignation

    TMEM43

    Sujet

    This gene belongs to the TMEM43 family. Defects in this gene are the cause of familial arrhythmogenic right ventricular dysplasia type 5 (ARVD5), also known as arrhythmogenic right ventricular cardiomyopathy type 5 (ARVC5). Arrhythmogenic right ventricular dysplasia is an inherited disorder, often involving both ventricles, and is characterized by ventricular tachycardia, heart failure, sudden cardiac death, and fibrofatty replacement of cardiomyocytes. This gene contains a response element for PPAR gamma (an adipogenic transcription factor), which may explain the fibrofatty replacement of the myocardium, a characteristic pathological finding in ARVC.

    Poids moléculaire

    44876

    ID gène

    79188

    NCBI Accession

    NP_077310

    UniProt

    Q9BTV4
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