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TMEM43 anticorps (AA 80-310)

TMEM43 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN6149266
  • Antigène Voir toutes TMEM43 Anticorps
    TMEM43 (Transmembrane Protein 43 (TMEM43))
    Épitope
    • 7
    • 6
    • 6
    • 6
    • 6
    • 1
    AA 80-310
    Reactivité
    • 21
    • 2
    Humain
    Hôte
    • 21
    Lapin
    Clonalité
    • 21
    Polyclonal
    Conjugué
    • 7
    • 4
    • 3
    • 3
    • 2
    • 2
    Cet anticorp TMEM43 est non-conjugé
    Application
    • 18
    • 16
    • 16
    • 1
    Western Blotting (WB)
    Séquence
    VAPENEGRLV HIIGALRTSK LLSDPNYGVH LPAVKLRRHV EMYQWVETEE SREYTEDGQV KKETRYSYNT EWRSEIINSK NFDREIGHKN PSAMAVESFM ATAPFVQIGR FFLSSGLIDK VDNFKSLSLS KLEDPHVDII RRGDFFYHSE NPKYPEVGDL RVSFSYAGLS GDDPDLGPAH VVTVIARQRG DQLVPFSTKS GDTLLLLHHG DFSAEEVFHR ELRSNSMKTW G
     Réactivité croisée
    Humain, Souris
    Attributs du produit
    Polyclonal Antibodies
    Immunogène
    Recombinant fusion protein containing a sequence corresponding to amino acids 80-310 of human TMEM43 (NP_077310.1).
    Isotype
    IgG
    Top Product
    Discover our top product TMEM43 Anticorps primaire
  • Indications d'application
    WB,1:500 - 1:2000
    Commentaires

    HIGH QUALITY

    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    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
    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène
    TMEM43 (Transmembrane Protein 43 (TMEM43))
    Autre désignation
    TMEM43 (TMEM43 Produits)
    Synonymes
    anticorps zgc:85946, anticorps ARVC5, anticorps ARVD5, anticorps EDMD7, anticorps LUMA, anticorps 1200015A22Rik, anticorps transmembrane protein 43, anticorps TMEM43, anticorps tmem43, anticorps 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.,TMEM43,ARVC5,ARVD5,EDMD7,LUMA,Signal Transduction,TMEM43
    Poids moléculaire
    44 kDa
    ID gène
    79188
    UniProt
    Q9BTV4
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