GTX113236 IP Image
GTX113236 IP Image
MYH9 antibody [N1-2], N-term
GTX113236
Product group Antibodies
Overview
- SupplierGeneTex
- Product NameMYH9 antibody [N1-2], N-term
- Delivery Days Customer9
- CertificationResearch Use Only
- Concentration0.43 mg/ml
- IsotypeIgG
- Scientific DescriptionThis 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. [provided by RefSeq]
- Storage Instruction2°C to 8°C,-20°C
- UNSPSC12352203
References
- Arv1 promotes cell division by recruiting IQGAP1 and myosin to the cleavage furrow. Sundvold H et al., 2016, Cell CycleRead more
- Centrosome guides spatial activation of Rac to control cell polarization and directed cell migration. Cheng HW et al., 2019 Feb, Life Sci AllianceRead more
- Comparative proteomic analysis of mouse models of pathological and physiological cardiac hypertrophy, with selection of biomarkers of pathological hypertrophy by integrative Proteogenomics. Kwon HK et al., 2018 Jul 23, Biochim Biophys Acta Proteins ProteomRead more
- Mass Spectrometry-Based Proteomics Identification of Enteropathogenic Escherichia coli Pedestal Constituents. Law HT et al., 2015 Jun 5, J Proteome ResRead more
- The E3 ligase Ubr3 regulates Usher syndrome and MYH9 disorder proteins in the auditory organs of Drosophila and mammals. Li T et al., 2016 Jun 22, ElifeRead more