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Myosin VI Antikörper

Der Kaninchen Polyklonal anti-Myosin VI Antikörper (ABIN5958676) detektiert spezifisch Myosin VI in WB, ELISA und IHC (p). Dieser Antikörper reagiert spezifisch mit Proben aus Human, Maus und Ratte.
Produktnummer ABIN5958676
449,00 €
Zzgl. Versandkosten 20,00 € und MwSt
Lieferung nach: Deutschland
Lieferung in 10 bis 13 Werktagen

Kurzübersicht für Myosin VI Antikörper (ABIN5958676)

Target

Alle Myosin VI (MYO6) Antikörper anzeigen
Myosin VI (MYO6)

Reaktivität

  • 19
  • 19
  • 18
  • 2
  • 1
Human, Maus, Ratte

Wirt

  • 32
  • 2
Kaninchen

Klonalität

  • 32
  • 2
Polyklonal

Konjugat

  • 15
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser Myosin VI Antikörper ist unkonjugiert

Applikation

  • 19
  • 17
  • 13
  • 13
  • 11
  • 8
  • 8
  • 6
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • Spezifität

    Deafness autosomal recessive 37,DFNA 22,DFNA22,DFNB 37,DFNB37,KIAA0389,MYO 6,Myo6,MYO6,Myosin VI,Myosin-VI,Myosin6,Unconventional myosin-6,Unconventional myosin-VI

    Aufreinigung

    Affinity purification

    Immunogen

    Synthesized peptide derived from the N-terminal region of human Myosin VI

    Isotyp

    IgG
  • Applikationshinweise

    WB 1:500-1:2000, IHC 1:100-300, ELISA 1:5000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Konzentration

    1 mg/mL

    Buffer

    PBS with 0.02 % sodium azide, 0.5 % BSA and 50 % glycerol,  pH 7.4

    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.
  • Target

    Myosin VI (MYO6)

    Andere Bezeichnung

    Myosin VI

    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. MYO6 (Myosin VI) is a Protein Coding gene. Diseases associated with MYO6 include Deafness, Autosomal Dominant 22 and Deafness, Autosomal Recessive 37. Among its related pathways are PAK Pathway and Vesicle-mediated transport. GO annotations related to this gene include actin binding and actin filament binding. An important paralog of this gene is MYO7A.

    Molekulargewicht

    150kDa

    Gen-ID

    4646

    UniProt

    Q9UM54

    Pathways

    Sensory Perception of Sound, Dicarboxylic Acid Transport, Asymmetric Protein Localization
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