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. NOP56 Antibody

NOP56 Antibody

  • 中文名稱：
    NOP56兔多克隆抗體
  • 貨號：
    CSB-PA015939GA01HU
  • 規(guī)格：
    ￥3,900
  • 其他：

產(chǎn)品詳情

  • Uniprot No.：
  • 基因名：
    NOP56
  • 別名：
    NOP56 antibody; NOL5ANucleolar protein 56 antibody; Nucleolar protein 5A antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human,Mouse,Rat
  • 免疫原：
    Human NOP56
  • 免疫原種屬：
    Homo sapiens (Human)
  • 抗體亞型：
    IgG
  • 純化方式：
    Antigen Affinity purified
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 產(chǎn)品提供形式：
    Liquid
  • 應(yīng)用范圍：
    ELISA,WB
  • 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(chǎn)品評價(jià)

靶點(diǎn)詳情

  • 功能：
    Involved in the early to middle stages of 60S ribosomal subunit biogenesis. Core component of box C/D small nucleolar ribonucleoprotein (snoRNP) particles. Required for the biogenesis of box C/D snoRNAs such U3, U8 and U14 snoRNAs.
  • 基因功能參考文獻(xiàn)：
    1. Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China, with its causative mutation as a hexanucleotide GGCCTG repeat expansion in intron 1 of the NOP56 gene, has been described. PMID: 26661328
    2. Studies indicate that the causative mutation for spinocerebellar ataxias SCA36, namely intronic hexanucleotide GGCCTG expansion in NOP56 gene, has been identified. PMID: 26663071
    3. We newly found intronic hexanucleotide GGCCTG gene expansion in NOP56 gene as the causative mutation in nine unrelated Japanese familial hereditary spinocerebellar ataxia patients PMID: 22353375
    4. This study demonistrated that NOP56 mutation is response spinocerebellar ataxia 36 in Spainish family. PMID: 22492559
    5. Expansion of the intronic GGCCTG hexanucleotide repeat in NOP56 causes a unique form of spinocerebellar ataxias, SCA36, which shows not only ataxia but also motor neuron dysfunction. PMID: 21683323
    6. hNop56p functions in the early to middle stages of 60 S subunit synthesis in human cells and has functional similarities with treacle-associated ribonucleoproteins PMID: 12777385
    7. Data demonstrate that fibrillarin and Nop56 directly interact in vivo, and that this interaction is indispensable for the association of both proteins with the box C/D snoRNPs. PMID: 19331828
    8. snoRNP assembly factor NUFIP can regulate the interactions between TIP48 and TIP49 and the core box C/D proteins. PMID: 19620283

    顯示更多

    收起更多

  • 相關(guān)疾病：
    Spinocerebellar ataxia 36 (SCA36)
  • 亞細(xì)胞定位：
    Nucleus, nucleolus. Cytoplasm. Nucleus, nucleoplasm.
  • 蛋白家族：
    NOP5/NOP56 family
  • 數(shù)據(jù)庫鏈接：

    HGNC: 15911

    OMIM: 614153

    KEGG: hsa:10528

    STRING: 9606.ENSP00000370589

    UniGene: Hs.376064



主站蜘蛛池模板： 老熟妇高潮一区二区三区| 久久精品国产99国产精2021| 国产超碰人人模人人爽人人添| 亚洲大尺度无码无码专线一区| 国产精品卡1卡2卡三卡四| 国色天香精品一卡2卡3卡4| 97se色综合一区二区二区| 亚洲精品永久在线观看| 中文字幕第一区高清av| 亚洲乱码日产精品bd在| 又大又紧又粉嫩18p少妇| 在线播放五十路熟妇| 超碰曰口干天天种夜夜爽 | 国产亚洲视频在线观看播放 | 蜜臀aⅴ国产精品久久久国产老师| 伊人久久大香线蕉av网站| 无码人妻精品一区二区三区下载| 少妇人妻真实偷人精品视频| 黑人糟蹋人妻hd中文字幕| 菠萝菠萝蜜午夜视频在线播放观看| 免费午夜福利不卡片在线播放| 国产精品成熟老女人| 欧美 国产日韩 综合在线| 少妇大叫太大太爽受不了在线观看| 性无码一区二区三区在线观看| 最新国产乱人伦偷精品免费网站| 亚洲午夜理论片在线观看| 在线天堂最新版资源| 国产口爆吞精在线视频2020版| 青青青国产免a在线观看| 午夜亚洲影院在线观看| 欧美丰满熟妇xxxx性ppx人交| av无码久久久久久不卡网站| 亚洲gv天堂无码男同在线观看| 又黄又爽又色视频| 欧美综合自拍亚洲综合图| 久久久久香蕉国产线看观看伊| 亚洲加勒比少妇无码av| 国产精品久久久久久av| 中国熟妇牲交视频| 手机在线亚洲国产精品|