OTOG Antibody
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) OTOG Polyclonal antibody
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Uniprot No.:Q6ZRI0
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基因名:OTOG
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别名:OTOG antibody; OTGN antibody; Otogelin antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Otogelin protein (1634-1796AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
本页面中的产品,OTOG Antibody (CSB-PA017273LA01HU),的标记方式是Non-conjugated。对于OTOG Antibody,我们还提供其他标记。见下表:
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:>95%, Protein G purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
产品提供形式:Liquid
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应用范围:ELISA, IHC, IF
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推荐稀释比:
Application Recommended Dilution IHC 1:200-1:500 IF 1:50-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
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功能:Glycoprotein specific to acellular membranes of the inner ear. May be required for the anchoring of the otoconial membranes and cupulae to the underlying neuroepithelia in the vestibule. May be involved in the organization and/or stabilization of the fibrillar network that compose the tectorial membrane in the cochlea. May play a role in mechanotransduction processes.
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基因功能参考文献:
- Patients with OTOG mutation show a flat to downsloping configuration of the audiogram with mild to moderate sensorineural hearing loss. Speech recognition scores remain good and vestibular hyporeflexia is present. PMID: 24378291
- study reports the identification of mutations in OTOG as a cause of moderate nonsyndromic hearing loss PMID: 23122587
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相关疾病:Deafness, autosomal recessive, 18B (DFNB18B)
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亚细胞定位:Apical cell membrane; Peripheral membrane protein; Extracellular side. Secreted, extracellular space.
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蛋白家族:Otogelin family
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数据库链接:
HGNC: 8516
OMIM: 604487
KEGG: hsa:340990
STRING: 9606.ENSP00000382323
UniGene: Hs.688380