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Conjugation/Formulation：Un-conjugated
- 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. [provided by RefSeq, Oct 2008]
- Immunogen A synthetic peptide of human TMEM43
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Gene ID
79188
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Swiss Prot
Q9BTV4
- Synonyms LUMA; ARVC5; ARVD5; EDMD7
- Reactivity Human,Mouse,Rat
- Application WB, IHC-P
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Recommended dilution
WB: 1:1000-1:10000
IHC-P: 1:200-1:500 - Calculated MW 45 kDa
- Observed MW 45 kDa
- Host species Rabbit
- Clonality Monoclonal
- Clonality No. DGR19564
- Isotype IgG
- Purity Affinity Purification
- Conjugation Un-conjugated
- Storage/Stability Store at -20°C. Supplied in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
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Western blot detection of TMEM43 in K562,C6 cell lysates using TMEM43 antibody(1:1000 diluted). -
Western blot analysis of extracts from C2C12，U2OS cells and Rat spleen，Mouse small intestine tissue using db13353 at 1:3000. -
Immunohistochemical analysis of paraffin-embedded human breast cancer using db13353 antibody.
订购信息
- Package Price (RMB)
- 10μL 398
- 20μL 698
- 50μL 1398
- 100μL 2398
- 货期：现货
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For research use only. Not intended for diagnostic.
