| Source: | Goat | Gene Id: | 4644 | 
| Isotype: | / | Swiss Prot: | Q9Y4I1 | 
| purity: | Affinity purification | 
| Background: | 
| This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq | 
| Reactivity | Human, Mouse | 
| Tested applications | WB ELISA IF | 
| Clonality | Polyclonal Antibody | 
| Calculated MW | 210 kDa | 
| Recommended Dilutions | 
                                     WB 1-3 ug/mL 
                                    
                                    IF 1-3 ug/mL 
                                    
                                    
                                    
                                    
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| Immunogen | A synthetic peptide corresponding to amino acids at internal region of human MYO5A | 
| Storage | Store at -20°C in Tris saline, pH7.3 (0.5% BSA, 0.02% sodium azide).Avoid freeze/thaw cycles. | 
| Synonym | GS1, MYH12, MYO5, MYR12 | 
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