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TMEM43 Antikörper (N-Term)

Dieser Anti-TMEM43 Antikörper ist ein Kaninchen Polyklonal Antikörper zur Detektion von TMEM43 in WB. Geeignet für Human.
Produktnummer ABIN5673734

Kurzübersicht für TMEM43 Antikörper (N-Term) (ABIN5673734)

Target

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

Reaktivität

  • 39
  • 22
  • 19
Human

Wirt

  • 39
Kaninchen

Klonalität

  • 21
  • 18
Polyklonal

Konjugat

  • 12
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Dieser TMEM43 Antikörper ist unkonjugiert

Applikation

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

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

    Sequenz

    ANYSSTSTRR EHVKVKTSSQ PGFLERLSET SGGMFVGLMA FLLSFYLIFT

    Aufreinigung

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N terminal region of human TMEM43
  • Applikationshinweise

    Optimal working dilution should be determined by the investigator.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

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

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

    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.
  • 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.

    Alias Symbols: LUMA, ARVC5, ARVD5, EDMD7

    Protein Size: 400

    Gen-ID

    79188

    NCBI Accession

    NM_024334, NP_077310

    UniProt

    Q9BTV4
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