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KD-Validated MYH9 Mouse Monoclonal Antibody
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KD-Validated MYH9 Mouse Monoclonal Antibody

KVAb00422-20ul · 20ul

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Catalog No: KVAb00422-20ul
Pack Size: 20ul
Brand: EnkiLife

Description

EnkiLife offers the KD-Validated MYH9 Mouse Monoclonal Antibody. This antibody reacts with Human and is suitable for WB,FCM,IHC-P application. The product boasts remarkable high specificity, outstanding reproducibility, and exceptional affinity, making it a reliable and superior choice for your needs. Dilution Ratio: WB 1:400-1:2,000; FC 1:100-1:1,000; IHC-P 1:500-1:1,000 Alternative Names of Immunogen:MYH9; Myosin Heavy Chain 9; NMHC-II-A; NMMHCA; EPSTS; FTNS; MHA; Cellular Myosin Heavy Chain, Type A; Nonmuscle Myosin Heavy Chain II-A; Non-Muscle Myosin Heavy Chain IIa; Non-Muscle Myosin Heavy Chain A; MMHC-IIA; Myosin-9; DFNA17; Myosin, Heavy Polypeptide 9, Non-Muscle; Non-Muscle Myosin Heavy Polypeptide 9; Myosin Heavy Chain, Non-Muscle IIa; Myosin, Heavy Chain 9, Non-Muscle; Non-Muscle Myosin Heavy Chain 9; Nonmuscle Myosin IIA2; NMMHC II-A; NMMHC-A; BDPLT6; MATINS 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. [provided by RefSeq, Dec 2011] Research Area: Signal Transduction

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