Recombinant TMEM43 monoklonaal antilichaam

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

Q9BTV4

Human; Mouse; Rat

Recombinant Human TMEM43 protein

UNQ; PRO; TMEM; ARVC; ARVD; EDMD; TMEM43; ARVC5; ARVD5; EDMD7; LUMA; UNQ2564; PRO6244

5B3

Unconjugated

WB

Tags & Cell Markers; Signal Transduction

Protein A

0.2 mg/mL

WB 1:1000-1:5000

PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Ice bag

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

https://789.bio/eb/QFRKFRQZ

44 kDa

44 kDa

IgG, κ