Myosin 9 Antikörper
Kurzübersicht für Myosin 9 Antikörper (ABIN6566485)
Target
Alle Myosin 9 (MYH9) Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
-
-
Aufreinigung
- Affinity purification
-
Immunogen
- Recombinant protein of human MYH9
-
Isotyp
- IgG
-
-
-
-
Applikationshinweise
- WB 1:1000 - 1:2000 IHC 1:50 - 1:100
-
Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
-
-
Konzentration
- 1 mg/mL
-
Buffer
- 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.
-
-
- Myosin 9 (MYH9)
-
Andere Bezeichnung
- MYH9
-
Hintergrund
-
Synonyms: BDPLT 6,BDPLT6,Cellular myosin heavy chain,Cellular myosin heavy chain type A,DFNA 17,DFNA17,EPSTS,FTNS,MGC104539,MHA,MYH 2A,MYH 9,MYH2A,MYH9,MYH9,MYHas8,MyHC 2A,MyHC IIa,MyHC2A,MyHCIIa,MYHSA 2,MYHSA2,Myosin 9,Myosin heavy chain 9,Myosin heavy chain 9 non muscle,Myosin heavy chain,Myosin heavy chain non muscle IIa,Myosin heavy chain nonmuscle IIa,Myosin heavy polypeptide 2,Myosin heavy polypeptide 9 non muscle,Myosin-9,Myosin9,NMHC II A,NMMHC A,NMMHC II a,NMMHC II-a,NMMHC IIA,NMMHC-A,NMMHC-IIA,NMMHCA,Non muscle myosin heavy chain A,Non muscle myosin heavy chain,Non muscle myosin heavy chain II A,Non muscle myosin heavy polypeptide 9,non-muscle IIa,Non-muscle myosin heavy chain A,Non-muscle myosin heavy chain IIa,Nonmuscle myosin heavy chain A,Nonmuscle myosin heavy chain II A,type A
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
-
Observed_MW: 250kDa
Calculated_MW: 159kDa/226kDa
-
Gen-ID
- 4627
-
UniProt
- P35579
-
Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
Target
-