MYO3A purified MaxPab rabbit polyclonal antibody (D01P)
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More Files
- More Functions
Western Blot (Transfected lysate)
Western Blot analysis of MYO3A expression in transfected 293T cell line (H00053904-T01) by MYO3A MaxPab polyclonal antibody.
Lane 1: MYO3A transfected lysate(27.60 KDa).
Lane 2: Non-transfected lysate.
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Specification
Product Description
Rabbit polyclonal antibody raised against a full-length human MYO3A protein.
Immunogen
MYO3A (AAH45538.1, 1 a.a. ~ 247 a.a) full-length human protein.
Sequence
MFPLIGKTIIFDNFPDPSDTWEITETIGKGTYGKVFKVLNKKNGQKAAVKILDPIHDIDEEIEAGYNILKALSDHPNVVRFYGIYFKKDKVNGDKLWLVLELCSGGSVTDLVKGFLKRGERMSEPLIAYILHEALMGLQHLHNNKTIHRDVKGNNILLTTEGGVKLVDFGVSAQLTSTRHRRNTSVGTPFWMAPEVIACEQQLDTTYDARCDTWSLGITAIELGDGDPPLADLHPMRALFKIPRSDD
Host
Rabbit
Reactivity
Human
Interspecies Antigen Sequence
Mouse (94)
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of MYO3A expression in transfected 293T cell line (H00053904-T01) by MYO3A MaxPab polyclonal antibody.
Lane 1: MYO3A transfected lysate(27.60 KDa).
Lane 2: Non-transfected lysate.
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Gene Info — MYO3A
Entrez GeneID
53904GeneBank Accession#
BC045538.1Protein Accession#
AAH45538.1Gene Name
MYO3A
Gene Alias
DFNB30
Gene Description
myosin IIIA
Gene Ontology
HyperlinkGene Summary
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
Other Designations
OTTHUMP00000019339
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Interactome
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Disease
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