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],

MYO5B抗体应用：WB 1:500-2000 ELISA 1:5000-20000myosin VB(MYO5B) Homo sapiens The protein encoded by this gene, together with other proteins, may be involved in plasma membrane recycling. Mutations in this gene are associated with microvillous inclusion disease. [provided by RefSeq, Sep 2009],

LRRDN抗体应用：WB 1:500-2000

LRRK2抗体应用：IHC-p 1:50-300leucine rich repeat kinase 2(LRRK2) Homo sapiens This gene is a member of the leucine-rich repeat kinase family and encodes a protein with an ankryin repeat region, a leucine-rich repeat (LRR) domain, a kinase domain, a DFG-like motif, a RAS domain, a GTPase domain, a MLK-like domain, and a WD40 domain. The protein is present largely in the cytoplasm but also associates with the mitochondrial outer membrane. Mutations in this gene have been associated with Parkinson disease-8. [provided by RefSeq, Jul 2008],

LRRN1抗体应用：WB 1:500-2000 ELISA 1:5000-20000similarity:Contains 1 fibronectin type-III domain.,similarity:Contains 1 Ig-like C2-type (immunoglobulin-like) domain.,similarity:Contains 11 LRR (leucine-rich) repeats.,

LRRT1抗体应用：WB 1:500-2000

LRRT2抗体应用：WB 1:500-2000