Myosin 9 antibody
Quick Overview for Myosin 9 antibody (ABIN7116598)
Target
See all Myosin 9 (MYH9) AntibodiesReactivity
Host
Clonality
Conjugate
Application
- 
    - 
                                            Purification
- Immunogen affinity purified
- 
                                            Purity
- ≥95 % as determined by SDS-PAGE
- 
                                            Immunogen
- myosin, heavy chain 9, non-muscle
- 
                                            Isotype
- IgG
 
- 
                                            
- 
    
- 
    - 
                                            Application Notes
- WB: 1:1000 - 1:2000, IHC: 1:50 - 1:100
- 
                                            Restrictions
- For Research Use only
 
- 
                                            
- 
    - 
                                            Format
- Liquid
- 
                                            Buffer
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
- 
                                            Preservative
- Sodium azide
- 
                                            Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 
                                            Storage
- -20 °C
- 
                                            Storage Comment
- -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
- 
                                            Expiry Date
- 12 months
 
- 
                                            
- 
    - Myosin 9 (MYH9)
- 
                                            Alternative Name
- MYH9
- 
                                            Background
- 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.
- 
                                            Molecular Weight
- 250 kDa
- 
                                            Gene ID
- 4627
- 
                                            UniProt
- P35579
- 
                                            Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
 Target
- 
                    
 
                                     
                                     
                                    