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TMEM43 anticorps (N-Term)

Cet anticorps anti-TMEM43 est un anticorps Lapin Polyclonal détectant TMEM43 dans WB. Adapté pour Humain.
N° du produit ABIN5673734

Aperçu rapide pour TMEM43 anticorps (N-Term) (ABIN5673734)

Antigène

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

Reactivité

  • 39
  • 22
  • 19
Humain

Hôte

  • 39
Lapin

Clonalité

  • 21
  • 18
Polyclonal

Conjugué

  • 12
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Cet anticorp TMEM43 est non-conjugé

Application

  • 34
  • 30
  • 13
  • 2
  • 1
Western Blotting (WB)
  • Épitope

    • 7
    • 6
    • 2
    • 1
    • 1
    • 1
    N-Term

    Séquence

    ANYSSTSTRR EHVKVKTSSQ PGFLERLSET SGGMFVGLMA FLLSFYLIFT

    Purification

    Affinity purified

    Immunogène

    The immunogen is a synthetic peptide directed towards the N terminal region of human TMEM43
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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

    -20 °C

    Stockage commentaire

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • 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.

    Alias Symbols: LUMA, ARVC5, ARVD5, EDMD7

    Protein Size: 400

    ID gène

    79188

    NCBI Accession

    NM_024334, NP_077310

    UniProt

    Q9BTV4
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