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TMEM43 antibody (N-Term)

This anti-TMEM43 antibody is a Rabbit Polyclonal antibody detecting TMEM43 in WB. Suitable for Human.
Catalog No. ABIN5673734

Quick Overview for TMEM43 antibody (N-Term) (ABIN5673734)

Target

See all TMEM43 Antibodies
TMEM43 (Transmembrane Protein 43 (TMEM43))

Reactivity

  • 39
  • 22
  • 19
Human

Host

  • 39
Rabbit

Clonality

  • 21
  • 18
Polyclonal

Conjugate

  • 12
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This TMEM43 antibody is un-conjugated

Application

  • 34
  • 30
  • 13
  • 2
  • 1
Western Blotting (WB)
  • Binding Specificity

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

    Sequence

    ANYSSTSTRR EHVKVKTSSQ PGFLERLSET SGGMFVGLMA FLLSFYLIFT

    Purification

    Affinity purified

    Immunogen

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

    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.

    Preservative

    Sodium azide

    Precaution of Use

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

    Storage

    -20 °C

    Storage Comment

    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))

    Alternative Name

    TMEM43

    Background

    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

    Gene ID

    79188

    NCBI Accession

    NM_024334, NP_077310

    UniProt

    Q9BTV4
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