TMEM43 Antikörper
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- Target Alle TMEM43 Antikörper anzeigen
- TMEM43 (Transmembrane Protein 43 (TMEM43))
- Reaktivität
- Human, Maus
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser TMEM43 Antikörper ist unkonjugiert
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Applikation
- Immunohistochemistry (IHC), Western Blotting (WB)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human TMEM43 (NP_077310.1).
- Isotyp
- IgG
- Top Product
- Discover our top product TMEM43 Primärantikörper
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anti-Transmembrane Protein 43 (TMEM43) (AA 80-310) antibody
TMEM43 Reaktivität: Human IHC, ELISA Wirt: Kaninchen Polyclonal unconjugated
anti-Transmembrane Protein 43 (TMEM43) (AA 178-312) antibodyTMEM43 Reaktivität: Human IHC, WB, ELISA Wirt: Kaninchen Polyclonal unconjugated
anti-Transmembrane Protein 43 (TMEM43) (AA 195-223) antibodyTMEM43 Reaktivität: Human WB, IHC (p) Wirt: Kaninchen Polyclonal RB32139 unconjugated
anti-Transmembrane Protein 43 (TMEM43) (AA 80-310) antibodyTMEM43 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
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- Applikationshinweise
- WB 1:500-1:2000 IHC 1:50-1:100
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- TMEM43 (Transmembrane Protein 43 (TMEM43))
- Andere Bezeichnung
- TMEM43 (TMEM43 Produkte)
- Synonyme
- zgc:85946 antikoerper, ARVC5 antikoerper, ARVD5 antikoerper, EDMD7 antikoerper, LUMA antikoerper, 1200015A22Rik antikoerper, transmembrane protein 43 antikoerper, TMEM43 antikoerper, tmem43 antikoerper, Tmem43 antikoerper
- Hintergrund
- 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.
- Molekulargewicht
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Observed_MW: 45 kDa
Calculated_MW: 44 kDa
- Gen-ID
- 79188
- UniProt
- Q9BTV4
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