Myosin VI Antikörper
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- Target Alle Myosin VI (MYO6) Antikörper anzeigen
- Myosin VI (MYO6)
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Reaktivität
- Human, Maus, Ratte
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser Myosin VI Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), Immunofluorescence (IF)
- Produktmerkmale
- Polyclonal Antibody
- Aufreinigung
- Affinity purification
- Immunogen
- Recombinant fusion protein of human MYO6 (NP_004990.3).
- Isotyp
- IgG
- Top Product
- Discover our top product MYO6 Primärantikörper
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anti-Myosin VI (MYO6) (N-Term) antibody
MYO6 Reaktivität: Human, Maus, Ratte WB, ELISA, IHC (p) Wirt: Kaninchen Polyclonal unconjugated
anti-Myosin VI (MYO6) (AA 1166-1195), (C-Term) antibodyMYO6 Reaktivität: Human WB, IF, IHC (p) Wirt: Kaninchen Polyclonal RB19127 unconjugated
anti-Myosin VI (MYO6) (AA 1188-1285) antibodyMYO6 Reaktivität: Human WB, ELISA Wirt: Maus Monoclonal 2E12 unconjugated
anti-Myosin VI (MYO6) (AA 1173-1203), (C-Term) antibodyMYO6 Reaktivität: Human WB, IF, IHC (p), EIA Wirt: Kaninchen Polyclonal unconjugated
anti-Myosin VI (MYO6) (N-Term) antibodyMYO6 Reaktivität: Human WB, ELISA Wirt: Kaninchen Polyclonal unconjugated
anti-Myosin VI (MYO6) (AA 1016-1285) antibodyMYO6 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
anti-Myosin VI (MYO6) (N-Term) antibodyMYO6 Reaktivität: Human, Maus, Ratte WB, ELISA, IHC (p) Wirt: Kaninchen Polyclonal unconjugated
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- Applikationshinweise
- WB 1:500-1:2000 IF 1:50-1:200
- 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
- Myosin VI (MYO6)
- Andere Bezeichnung
- MYO6 (MYO6 Produkte)
- Hintergrund
- This gene encodes a reverse-direction motor protein that moves toward the minus end of actin filaments and plays a role in intracellular vesicle and organelle transport. The protein consists of a motor domain containing an ATP- and an actin-binding site and a globular tail which interacts with other proteins. This protein maintains the structural integrity of inner ear hair cells and mutations in this gene cause non-syndromic autosomal dominant and recessive hearing loss. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
- Molekulargewicht
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Observed_MW: 150 kDa
Calculated_MW: 145 kDa/146 kDa/148 kDa/149 kDa
- Gen-ID
- 4646
- UniProt
- Q9UM54
- Pathways
- Sensory Perception of Sound, Dicarboxylic Acid Transport, Asymmetric Protein Localization
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