Myosin 9 Antikörper (N-Term)
Kurzübersicht für Myosin 9 Antikörper (N-Term) (ABIN2855153)
Target
Alle Myosin 9 (MYH9) Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
Güteklasse
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Bindungsspezifität
- N-Term
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Spezifität
- This antibody may cross react with MYH10, MYH14, or other family members.
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Kreuzreaktivität
- Human
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Produktmerkmale
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Rabbit Polyclonal antibody to MYH9 (myosin, heavy chain 9, non-muscle)
MYH9 antibody [N1], N-term -
Aufreinigung
- Purified by antigen-affinity chromatography.
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Immunogen
- Recombinant protein encompassing a sequence within the N-terminus region of human MYH9. The exact sequence is proprietary.
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Isotyp
- IgG
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Applikationshinweise
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. IP: 1:100-1:500. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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Kommentare
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Positive Control: U87-MG , SK-N-SH , IMR32 , SK-N-AS , NT2D1 , PC-3
Validation: KO/KD, Overexpression
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Beschränkungen
- Nur für Forschungszwecke einsetzbar
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Format
- Liquid
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Konzentration
- 1.31 mg/mL
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Buffer
- 1XPBS pH 7, 20 % Glycerol, 0.025 % ProClin 300
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Konservierungsmittel
- ProClin
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Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Lagerung
- 4 °C,-20 °C
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Informationen zur Lagerung
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Myosin 9 (MYH9)
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Andere Bezeichnung
- myosin heavy chain 9
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Hintergrund
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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.
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Molekulargewicht
- 227 kDa
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Gen-ID
- 4627
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UniProt
- P35579
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Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
Target
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