Myosin 9 Antikörper (pTyr158)

Produktnummer ABIN1539741

Dieses Anti-Myosin 9-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von Myosin 9 in DB. Geeignet für Human. Dieses Primary Antibody wurde in 1 Publikation zitiert.

Kurzübersicht für Myosin 9 Antikörper (pTyr158) (ABIN1539741)

Target: Myosin 9 (MYH9)

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser Myosin 9 Antikörper ist unkonjugiert

Applikation: Dot Blot (DB)

Klon: RB36361

Produktdetails anti-Myosin 9 Antikörper

Bindungsspezifität: pTyr158

Homologie: C, M, Rat

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This MYH9 Antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding Y158 of human MYH9.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: DB: 1:500

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: Phospho-MYH9-Y158 Antibody can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the Phospho-MYH9-Y158 Antibody at -20 °C.

Haltbarkeit: 6 months

Referenzen für anti-Myosin 9 Antikörper (ABIN1539741)

Almeida, Mesquita, Cruz, Osório, Custódio, Brito, Vingadassalom, Martins, Leong, Holden, Cabanes, Sousa: "Src-dependent tyrosine phosphorylation of non-muscle myosin heavy chain-IIA restricts Listeria monocytogenes cellular infection." in: The Journal of biological chemistry, Vol. 290, Issue 13, pp. 8383-95, (2015) (PubMed).

Details zu Myosin 9

Target: Myosin 9 (MYH9)

Andere Bezeichnung: MYH9

Hintergrund: This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of 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: 226532

Gen-ID: 4627

NCBI Accession: NP_002464

UniProt: P35579

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