TMEM43 Products
(Transmembrane Protein 43 (TMEM43))
Categories
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. [provided by RefSeq, Oct 2008].
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Featured TMEM43 Categories
TMEM43 Antibodies
High quality antibodies with extensive validation data.
Recommended TMEM43 Antibodies
Product
Reactivity
Application
Validations
Cat. No.
Quantity
Datasheet
Reactivity
Human
Application
IHC, ELISA
Validations
- (2)
Cat. No.
ABIN7173219
Quantity
100 μL
Datasheet
Datasheet
Reactivity
Human
Application
IHC, ELISA, WB
Validations
- (2)
Cat. No.
ABIN7173215
Quantity
100 μg
Datasheet
Datasheet
Reactivity
Human
Application
WB, IHC (p)
Validations
- (2)
Cat. No.
ABIN656549
Quantity
400 μL
Datasheet
Datasheet
Latest Publications for our TMEM43 products
: "Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy." in: Clinical genetics, Vol. 80, Issue 3, pp. 256-64, (2011) (PubMed).Synonyms and alternative names related to TMEM43
transmembrane protein 43 (TMEM43), transmembrane protein 43 (tmem43), transmembrane protein 43 (Tmem43), 1200015A22Rik, ARVC5, ARVD5, EDMD7, LUMA, zgc:85946Protein level used designations for TMEM43
- elastin
- transmembrane protein 43
- Transmembrane protein 43
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