TMEM43 anticorps
-
- Antigène Voir toutes TMEM43 Anticorps
- TMEM43 (Transmembrane Protein 43 (TMEM43))
- Reactivité
- Humain, Souris
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp TMEM43 est non-conjugé
-
Application
- Immunohistochemistry (IHC), Western Blotting (WB)
- Attributs du produit
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein of human TMEM43 (NP_077310.1).
- Isotype
- IgG
- Top Product
- Discover our top product TMEM43 Anticorps primaire
-
anti-Transmembrane Protein 43 (TMEM43) (AA 80-310) antibody
TMEM43 Reactivité: Humain IHC, ELISA Hôte: Lapin Polyclonal unconjugated
anti-Transmembrane Protein 43 (TMEM43) (AA 178-312) antibodyTMEM43 Reactivité: Humain IHC, WB, ELISA Hôte: Lapin Polyclonal unconjugated
anti-Transmembrane Protein 43 (TMEM43) (AA 195-223) antibodyTMEM43 Reactivité: Humain WB, IHC (p) Hôte: Lapin Polyclonal RB32139 unconjugated
anti-Transmembrane Protein 43 (TMEM43) (AA 80-310) antibodyTMEM43 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
-
- Indications d'application
- WB 1:500-1:2000 IHC 1:50-1:100
- Restrictions
- For Research Use only
-
- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
-
- Antigène
- TMEM43 (Transmembrane Protein 43 (TMEM43))
- Autre désignation
- TMEM43 (TMEM43 Produits)
- Synonymes
- anticorps zgc:85946, anticorps ARVC5, anticorps ARVD5, anticorps EDMD7, anticorps LUMA, anticorps 1200015A22Rik, anticorps transmembrane protein 43, anticorps TMEM43, anticorps tmem43, anticorps Tmem43
- Sujet
- 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.
- Poids moléculaire
-
Observed_MW: 45 kDa
Calculated_MW: 44 kDa
- ID gène
- 79188
- UniProt
- Q9BTV4
-
