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RPGRIP1-Like (RPGRIP1L) (N-Term) Peptide

RPGRIP1L 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN5511911
发货至: 中国
  • 抗原 See all RPGRIP1L products
    RPGRIP1L (RPGRIP1-Like (RPGRIP1L))
    蛋白结构域
    N-Term
    宿主
    资源
    • 3
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    HARKQEDKIK RMATKLIRLV NDKKRYERVG GGPKRLGRDV EMEEMIEQLQ
    产品特性
    This is a synthetic peptide designed for use in combination with anti-FTM Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
  • 应用备注
    Optimal working dilution should be determined by the investigator.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    RPGRIP1L (RPGRIP1-Like (RPGRIP1L))
    别名
    si:ch1073-301i20.1 Peptide, mks5 Peptide, cors3 Peptide, jbts7 Peptide, nphp8 Peptide, CORS3 Peptide, FTM Peptide, JBTS7 Peptide, MKS5 Peptide, NPHP8 Peptide, 1700047E16Rik Peptide, 4931437C01 Peptide, Ftm Peptide, Nphp8 Peptide, RGD1311099 Peptide, RPGRIP1 like Peptide, RPGRIP1-like Peptide, Protein fantom Peptide, Rpgrip1-like Peptide, RPGRIP1L Peptide, rpgrip1l Peptide, mks-5 Peptide, Rpgrip1l Peptide
    背景
    The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). Two transcript variants encoding different isoforms have been found for this gene.

    Alias Symbols: RPGRIP1L,FTM,KIAA1005,NPHP8,

    Protein Size: 1315
    基因ID
    23322
    NCBI登录号
    NP_056087
    UniProt
    Q68CZ1
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