Myosin 9 Antikörper (N-Term)
Kurzübersicht für Myosin 9 Antikörper (N-Term) (ABIN6243267)
Target
Alle Myosin 9 (MYH9) Antikörper anzeigenReaktivität
Wirt
Klonalität
Konjugat
Applikation
Klon
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    - 
                                            Bindungsspezifität
- AA 134-165, N-Term
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                                            Homologie
- C, Rat
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                                            Aufreinigung
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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                                            Immunogen
- This MYH9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 134-165 amino acids from the N-terminal region of human MYH9.
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                                            Isotyp
- Ig Fraction
 
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    - 
                                            Applikationshinweise
- WB: 1:1000. WB: 1:1000. FC: 1:10~50
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                                            Beschränkungen
- Nur für Forschungszwecke einsetzbar
 
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    - 
                                            Format
- Liquid
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                                            Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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                                            Konservierungsmittel
- Sodium azide
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                                            Vorsichtsmaßnahmen
- This product contains Sodium azide: 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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                                            Haltbarkeit
- 6 months
 
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    - Myosin 9 (MYH9)
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                                            Andere Bezeichnung
- MYH9
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                                            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.
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                                            Molekulargewicht
- 226532
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                                            NCBI Accession
- NP_002464
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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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