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Invitrogen™ TMEM43 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA548409
Description
Predicted to react with mouse and rat based on sequence homology.
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.
Specifications
TMEM43 | |
Polyclonal | |
Unconjugated | |
TMEM43 | |
1200015A22Rik; ARVC5; ARVD5; EDMD7; LUMA; Protein LUMA; Tmem43; Transmembrane protein 43; UNQ2564/PRO6244 | |
Rabbit | |
Antigen affinity chromatography, Protein A | |
RUO | |
79188 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
0.3 mg/mL | |
PBS with 0.09% sodium azide; pH 7.4 | |
Q9BTV4 | |
TMEM43 | |
KLH conjugated synthetic peptide between 195-223 amino acids from the Central region of human TMEM43. | |
400 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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