产品详情 |
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Antigenic Specificity | MYH9 |
Clone | polyclonal |
Host Species | Rabbit |
Reactive Species | human |
Isotype | n/a |
Format | peptide affinity purified |
Size | 80 µl, 400 µl |
Concentration | n/a |
Applications | WB. RUO |
Reviews / Ratings | If you have used this antibody, please help fellow researchers by submitting reviews to pAbmAbs and antYbuddY. |
Description | 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. This MYH9 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1840-1867 amino acids from the C-terminal region of human MYH9. |
Immunogen | Human MYH9. |
Other Names | Cellular Myosin Heavy Chain; Type A Myosin Heavy Chain 9 Myosin Heavy Chain; Non-Muscle Iia Non-Muscle Myosin Heavy Chain A; Nmmhc-A; Non-Muscle Myosin Heavy Chain Iia; Nmmhc Ii-A; Nmmhc-Iia; MYH9; BDPLT6; FTNS; MHA; Myosin heavy chain 9; Myosin-9; DFNA17; EPSTS; NMHC-II-A; NMMHCA; MGC104539; Myosin Iia; type A; Myosin heavy chain; non-muscle IIa; Non-muscle myosin heavy chain A |
Gene, Accession # | MYH9, SwissProt: P35579 |
Catalog # | abx030030 |
Price | |
Order / More Info | MYH9 Antibody from ABBEXA |
Product Specific References | n/a |
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