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Rho-related GTP-binding protein 抗体

RhO (pan) 适用: Cow WB, IHC 宿主: 小鼠 Monoclonal 1D4 unconjugated
产品编号 ABIN361366
发货至: 中国
  • 抗原 See all Rho-related GTP-binding protein (RhO (pan)) 抗体
    Rho-related GTP-binding protein (RhO (pan))
    适用
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    Cow
    宿主
    • 23
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    小鼠
    克隆类型
    • 23
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    单克隆
    标记
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    This Rho-related GTP-binding protein antibody is un-conjugated
    应用范围
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    Western Blotting (WB), Immunohistochemistry (IHC)
    特异性
    Specific for the ~ 39k rhodopsin protein.
    交叉反应
    Amphibian, 哺乳动物
    纯化方法
    Protein G purified culture supernatant
    免疫原
    Purified native bovine rhodopsin
    克隆位点
    1D4
    亚型
    IgG1
    Top Product
    Discover our top product RhO (pan) Primary Antibody
  • 应用备注
    Recommended Dilution: WB: 1:1000 IHC: 1:100 Quality Control: Western blots performed on each lot.
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    100 μL in 10 mM HEPES (  pH 7.5), 150 mM NaCl, 100 μg per ml BSA and 50 % glycerol.
    储存条件
    -20 °C
  • Cho, Song, Shin, Kim: "Neonatal disease environment limits the efficacy of retinal transplantation in the LCA8 mouse model." in: BMC ophthalmology, Vol. 16, Issue 1, pp. 193, (2017) (PubMed).

    Kim, Park, Lee, Shin, Nickas, Kim, Cho: "Yap is essential for retinal progenitor cell cycle progression and RPE cell fate acquisition in the developing mouse eye." in: Developmental biology, Vol. 419, Issue 2, pp. 336-347, (2017) (PubMed).

  • 抗原
    Rho-related GTP-binding protein (RhO (pan))
    别名
    RHO (RhO (pan) 产品)
    物质类
    Chemical
    背景
    Rhodopsin is a photoreceptor protein found in retinal rods. It is a complex formed by the binding of retinaldehyde, the oxidized form of retinol, to the protein opsin and undergoes a series of complex reactions in response to visible light resulting in the transmission of nerve impulses to the brain. Mutation of the rhodopsin gene is a major contributor to various retinopathies such as retinitis pigmentosa. The disease-causing protein generally aggregates with ubiquitin in inclusion bodies, disrupts the intermediate filament network and impairs the ability of the cell to degrade non-functioning proteins which leads to photoreceptor apoptosis (Berson et al., 1991). Other mutations on rhodopsin lead to X-linked congenital stationary night blindness, mainly due to constitutive activation, when the mutations occur around the chromophore binding pocket of rhodopsin (Dryja et al.,1993). Several other pathological states relating to rhodopsin have been discovered including poor post-Golgi trafficking, dysregulative activation, rod outer segment instability and arrestin binding. Anti-Rhodopsin Immunohistochemical staining of mouse retinal section showing specific immunolabeling of the rhodopsin protein in the rod spherules. Photo courtesy of Mary Raven, University of California, Santa Barbara, CA.
    分子量
    '39 kDa
    基因ID
    509933
    UniProt
    P02699
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