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Protein structure
MYH9
Myosin heavy chain 9DFNA17, EPSTS, FTNS, MHA, NMHC-II-A, NMMHCA
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. [provided by RefSeq, Dec 2011]
Top validated antibodies |
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| Proteintech Group |  11128-1-AP |
33 references | Polyclonal |
WB
EL
ICC
IP
IHC
FC
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| Invitrogen Antibodies | 11128-1-AP |
Polyclonal |
WB
ICC
IP
IHC
FC
OA
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| GeneTex | GTX113236 |
5 references | Polyclonal |
WB
ICC
IP
IHC
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| Novus Biologicals | H00004627-M06 |
2 references | Monoclonal |
WB
EL
ICC
IP
IHC
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| LSBio | LS-B5936 |
Monoclonal |
WB
EL
ICC
IHC
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