MYLK2抗体应用：WB 1:500-2000 ELISA 1:5000-20000myosin light chain kinase 2(MYLK2) Homo sapiens This gene encodes a myosin light chain kinase, a calcium/calmodulin dependent enzyme, that is exclusively expressed in adult skeletal muscle. [provided by RefSeq, Jul 2008],

MYNN抗体应用：WB 1:500-2000This gene encodes a member of the BTB/POZ and zinc finger domain-containing protein family that are involved in the control of gene expression. Alternative splicing results in multiple transcript variants and a pseudogene has been identified on chromosome 14. [provided by RefSeq, Jun 2010],

MYO10抗体应用：WB 1:500-2000 ELISA 1:5000-20000myosin X(MYO10) Homo sapiens This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional non-muscle myosin-10 (MYH10). Unconventional myosins contain the basic domains of conventional myosins and are further distinguished from class members by their tail domains. This gene functions as an actin-based molecular motor and plays a role in integration of F-actin and microtubule cytoskeletons during meiosis. [provided by RefSeq, Dec 2011],

MYO15抗体应用：IHC-p 1:50-300myosin XVA(MYO15A) Homo sapiens This gene encodes an unconventional myosin. This protein differs from other myosins in that it has a long N-terminal extension preceding the conserved motor domain. Studies in mice suggest that this protein is necessary for actin organization in the hair cells of the cochlea. Mutations in this gene have been associated with profound, congenital, neurosensory, nonsyndromal deafness. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Read-through transcripts containing an upstream gene and this gene have been identified, but they are not thought to encode a fusion protein. Several alternatively spliced transcript variants have been described, but their full length sequences have not been determined. [provided by RefSeq, Jul 2008],

MYO19抗体应用：WB 1:500-2000

MYO1A 抗体应用：WB 1:500-2000 ELISA 1:5000-20000myosin IA(MYO1A) Homo sapiens This gene encodes a member of the myosin superfamily. The protein represents an unconventional myosin; it should not be confused with the conventional skeletal muscle myosin-1 (MYH1). Unconventional myosins contain the basic domains characteristic of conventional myosins and are further distinguished from class members by their tail domains. They function as actin-based molecular motors. Mutations in this gene have been associated with autosomal dominant deafness. Alternatively spliced variants have been found for this gene. [provided by RefSeq, Dec 2011],

MYO1B抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Motor protein that may participate in process critical to neuronal development and function such as cell migration, neurite outgrowth and vesicular transport.,similarity:Contains 1 myosin head-like domain.,similarity:Contains 6 IQ domains.,

MYO1F抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Myosins are actin-based motor molecules with ATPase activity. Unconventional myosins serve in intracellular movements. Their highly divergent tails are presumed to bind to membranous compartments, which would be moved relative to actin filaments.,similarity:Contains 1 IQ domain.,similarity:Contains 1 myosin head-like domain.,similarity:Contains 1 SH3 domain.,

MYO3A抗体应用：WB 1:500-2000 ELISA 1:5000-20000myosin IIIA(MYO3A) Homo sapiens The protein encoded by this gene belongs to the myosin superfamily. Myosins are actin-dependent motor proteins and are categorized into conventional myosins (class II) and unconventional myosins (classes I and III through XV) based on their variable C-terminal cargo-binding domains. Class III myosins, such as this one, have a kinase domain N-terminal to the conserved N-terminal motor domains and are expressed in photoreceptors. The protein encoded by this gene plays an important role in hearing in humans. Three different recessive, loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss. Expression of this gene is highly restricted, with the strongest expression in retina and cochlea. [provided by RefSeq, Jul 2008],

MYO3B抗体应用：WB 1:500-2000 ELISA 1:5000-20000myosin IIIB(MYO3B) Homo sapiens This gene encodes one of the class III myosins. Myosins are ATPases, activated by actin, that move along actin filaments in the cell. This class of myosins are characterized by an amino-terminal kinase domain and shown to be present in photoreceptors. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014],