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TMEM43 Antikörper (AA 195-223)

Der Kaninchen Polyklonal Anti-TMEM43-Antikörper wurde für WB und IHC (p) validiert. Er ist geeignet, TMEM43 in Proben von Human zu detektieren.
Produktnummer ABIN656549

Kurzübersicht für TMEM43 Antikörper (AA 195-223) (ABIN656549)

Target

Alle TMEM43 Antikörper anzeigen
TMEM43 (Transmembrane Protein 43 (TMEM43))

Reaktivität

  • 19
  • 3
  • 1
Human

Wirt

  • 19
Kaninchen

Klonalität

  • 17
  • 2
Polyklonal

Konjugat

  • 10
  • 3
  • 2
  • 2
  • 1
  • 1
Dieser TMEM43 Antikörper ist unkonjugiert

Applikation

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

Klon

RB32139
  • Bindungsspezifität

    • 7
    • 6
    • 2
    • 1
    • 1
    • 1
    AA 195-223

    Homologie

    M, Rat

    Aufreinigung

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

    Immunogen

    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.

    Isotyp

    Ig Fraction
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

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

    Haltbarkeit

    6 months
  • Target

    TMEM43 (Transmembrane Protein 43 (TMEM43))

    Andere Bezeichnung

    TMEM43

    Hintergrund

    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.

    Molekulargewicht

    44876

    Gen-ID

    79188

    NCBI Accession

    NP_077310

    UniProt

    Q9BTV4
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