在线日韩日本国产亚洲丨少妇伦子伦情品无吗丨欧美性猛交xxxx免费看蜜桃丨精品人妻系列无码一区二区三区丨亚洲精品无码不卡在线播放

Your Good Partner in Biology Research

  1. Home
  2. 抗體
  3. 多克隆抗體
  4. PEX10 Antibody

PEX10 Antibody

  • 中文名稱：
    PEX10兔多克隆抗體
  • 貨號：
    CSB-PA869145
  • 規格：
    ￥2024
  • 圖片：
    • Western blot analysis of extracts from Jurkat cells, using PEX10 antibody.
    • Immunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue using PEX10 antiobdy.
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) PEX10 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    PEX10
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Synthesized peptide derived from internal of Human PEX10.
  • 免疫原種屬：
    Homo sapiens (Human)
  • 克隆類型：
    Polyclonal
  • 純化方式：
    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 產品提供形式：
    Liquid
  • 應用范圍：
    ELISA,WB,IHC
  • 推薦稀釋比：
    Application Recommended Dilution
    WB 1:500-1:3000
    IHC 1:50-1:100
  • Protocols：
  • 儲存條件：
    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • 貨期：
    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.
  • 用途：
    For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產品評價

靶點詳情

  • 功能：
    Somewhat implicated in the biogenesis of peroxisomes.
  • 基因功能參考文獻：
    1. This study demonstrated that two mutations in PEX10 were found in the three peroxisomal biogenesis disorders patients: c.827G>T (novel) causing the missense change p.Cys276Phe and c.932G>A causing the missense change p.Arg311Gln. PMID: 27230853
    2. abnormal expression of PEX10 gene resulting from copy number variations of 1p36 region may be associated with the epilepsy phenotype PMID: 25636090
    3. child and an adult of normal intelligence with progressive ataxia, axonal motor neuropathy, decreased vibration sense and cerebellar atrophy; 2 mutations in PEX10 found in child, c.992G>A and c.764_765insA, and in the adult, c.2T>C and c.790C>T PMID: 20695019
    4. Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. PMID: 14713216
    5. the relative fraction of disease-causing alleles that occur in the coding and splice junction sequences of PEX10 gene. PMID: 19105186

    顯示更多

    收起更多

  • 相關疾病：
    Peroxisome biogenesis disorder complementation group 7 (PBD-CG7); Peroxisome biogenesis disorder 6A (PBD6A); Peroxisome biogenesis disorder 6B (PBD6B)
  • 亞細胞定位：
    Peroxisome membrane; Peripheral membrane protein.
  • 蛋白家族：
    Pex2/pex10/pex12 family
  • 數據庫鏈接：

    HGNC: 8851

    OMIM: 602859

    KEGG: hsa:5192

    UniGene: Hs.732228



主站蜘蛛池模板： 国产伦精品一区二区三区免.费| 超碰97人人做人人爱亚洲尤物| 人人妻人人爽日日人人| 精品偷拍一区二区三区在线看| 草草影院发布页| 亚洲爆乳无码专区www| 吃奶摸下高潮60分钟免费视频| 伊人久久精品av一区二区 | 国产69精品久久久久999小说| 羞羞色男人的天堂| 在线资源天堂www| 成人免费无码大片a毛片抽搐| 丁香五香天堂网| 国产精品被窝福利一区| 又粗又硬又黄又爽的视频永久| 放荡的少妇2欧美版| 成人做爰www网站视频| 蕾丝av无码专区在线观看| 欲妇荡岳丰满少妇岳| 国产伦孑沙发午休精品| 亚洲精品久久久久久无码色欲四季| 狼友av永久网站免费观看孕交| 久久精品亚洲中文字幕无码麻豆| 国产高清在线精品一区| 99re6热视频这里只精品首页 | 毛片无码国产| 国内少妇偷人精品免费| 奇米777狠狠色噜噜狠狠狠| 亚洲欧洲精品成人久久曰影片| 亚洲国产成人一区二区精品区| 亚洲毛片无码不卡av在线播放| 麻豆成人av不卡一二三区| 中文字幕av无码一区二区三区 | 国产成人精选在线观看不卡| 麻豆网神马久久人鬼片| 黑人玩弄人妻1区二区| 国产成人年无码av片在线观看| 特级毛片内射www无码| 久久久久久久女国产乱让韩| 日韩av无码一区二区三区无码 | 日韩精品一区二区在线观看|