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TMEM43 antibody (AA 195-223)

The Rabbit Polyclonal anti-TMEM43 antibody has been validated for WB and IHC (p). It is suitable to detect TMEM43 in samples from Human.
Catalog No. ABIN656549

Quick Overview for TMEM43 antibody (AA 195-223) (ABIN656549)

Target

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

Reactivity

  • 19
  • 3
  • 1
Human

Host

  • 19
Rabbit

Clonality

  • 17
  • 2
Polyclonal

Conjugate

  • 10
  • 3
  • 2
  • 2
  • 1
  • 1
This TMEM43 antibody is un-conjugated

Application

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

Clone

RB32139
  • Binding Specificity

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

    Predicted Reactivity

    M, Rat

    Purification

    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.

    Isotype

    Ig Fraction
  • Application Notes

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

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

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

    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

    4 °C,-20 °C

    Storage Comment

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

    Expiry Date

    6 months
  • 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.

    Molecular Weight

    44876

    Gene ID

    79188

    NCBI Accession

    NP_077310

    UniProt

    Q9BTV4
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