MYO5A Antikörper

Produktnummer ABIN7264882

Produktdetails anti-MYO5A Antikörper

Target: MYO5A (Myosin VA (MYO5A))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser MYO5A Antikörper ist unkonjugiert

Applikation: Immunohistochemistry (IHC)

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Affinity purification

Immunogen: Recombinant fusion protein of human MYO5A (NP_000250.3).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IHC 1:50-1:100

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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.

Details zu MYO5A

Target: MYO5A (Myosin VA (MYO5A))

Andere Bezeichnung: MYO5A (MYO5A Produkte)

Synonyme: myo5a antikoerper, MGC53270 antikoerper, si:dkey-266j9.1 antikoerper, MYOA antikoerper, MYO5A antikoerper, D antikoerper, Dop antikoerper, Myh12 antikoerper, 9630007J19Rik antikoerper, AI413174 antikoerper, AI661011 antikoerper, Dbv antikoerper, MVa antikoerper, Myo5 antikoerper, MyoVA antikoerper, Sev-1 antikoerper, d antikoerper, d-120J antikoerper, flail antikoerper, flr antikoerper, DILUTE antikoerper, myoxin) antikoerper, non-muscle antikoerper, GS1 antikoerper, MYH12 antikoerper, MYO5 antikoerper, MYR12 antikoerper, myosin VA L homeolog antikoerper, myosin VAa antikoerper, myosin VA antikoerper, myosin va antikoerper, myo5a.L antikoerper, myo5aa antikoerper, MYO5A antikoerper, PY04789 antikoerper, Myo5a antikoerper

Hintergrund: This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined.

Gen-ID: 4644

UniProt: Q9Y4I1

Pathways: Hormone Transport, Peptide Hormone Metabolism