Myosin 9 Antikörper

Produktnummer ABIN5701128

Dieses Anti-Myosin 9-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von Myosin 9 in WB, ELISA, IHC, IF und IP. Geeignet für Human, Maus, Ratte und Zebrafisch (Danio rerio).

Kurzübersicht für Myosin 9 Antikörper (ABIN5701128)

Target: Myosin 9 (MYH9)

Reaktivität: Human, Maus, Ratte, Zebrafisch (Danio rerio)

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Myosin 9 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF), Immunoprecipitation (IP)

Produktdetails anti-Myosin 9 Antikörper

Immunogen: myosin, heavy chain 9, non-muscle

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Kommentare:

mouse kidney tissue were subjected to SDS PAGE followed by western blot with FNab05479(MYH9 antibody) at dilution of 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Buffer: PBS with 0.02 % sodium azide and 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.

Handhabung: Avoid repeated freeze / thaw cycles.

Lagerung: -20 °C

Haltbarkeit: 12 months

Details zu Myosin 9

Target: Myosin 9 (MYH9)

Andere Bezeichnung: MYH9

Hintergrund: Synonyms:BDPLT6 Background:This gene encodes a conventional non-muscle myosin, this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.

Molekulargewicht: 224 kDa

Gen-ID: 4627

UniProt: P35579

Pathways: Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex