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

KCTD7 Antibody, HRP conjugated

  • 中文名稱:
    KCTD7兔多克隆抗體, HRP偶聯
  • 貨號:
    CSB-PA850395LB01HU
  • 規格:
    ¥880
  • 其他:

產品詳情

  • 產品名稱:
    Rabbit anti-Homo sapiens (Human) KCTD7 Polyclonal antibody
  • Uniprot No.:
  • 基因名:
    KCTD7
  • 別名:
    KCTD7 antibody; BTB/POZ domain-containing protein KCTD7 antibody
  • 宿主:
    Rabbit
  • 反應種屬:
    Human
  • 免疫原:
    Recombinant Human BTB/POZ domain-containing protein KCTD7 protein (5-152AA)
  • 免疫原種屬:
    Homo sapiens (Human)
  • 標記方式:
    HRP
  • 克隆類型:
    Polyclonal
  • 抗體亞型:
    IgG
  • 純化方式:
    >95%, Protein G purified
  • 濃度:
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液:
    Preservative: 0.03% Proclin 300
    Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
  • 產品提供形式:
    Liquid
  • 應用范圍:
    ELISA
  • 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:
    May be involved in the control of excitability of cortical neurons.
  • 基因功能參考文獻:
    1. KCTD7 has an impact on K+ fluxes, neurotransmitter synthesis and neuronal function, and that malfunction of the encoded protein may lead to progressive myoclonus epilepsy. PMID: 27742667
    2. reviews the phenotype of progressive myoclonic epilepsy associated with KCTD7 mutations [review] PMID: 27629772
    3. This study identified that novel KCTD7 mutation in patients with progressive myoclonus epilepsy with ataxia. PMID: 25060828
    4. The KCTD7 gene, previously associated with progressive myoclonus epilepsies (PMEs) in a single inbred family, was screened for mutations in 18 Turkish PME patients. PMID: 22693283
    5. this study clearly demonstrates that KCTD7 mutations also cause a rare, infantile-onset NCL subtype designated as CLN14. PMID: 22748208
    6. We found a C to T mutation in exon 2 of the potassium channel tetramerization domain containing 7 gene(KCTD7)in a progressive myoclonic epilepsy family affecting a highly conserved segment of the predicted protein changing an arginine codon to a stop. PMID: 17455289

    顯示更多

    收起更多

  • 相關疾?。?/div>
    Epilepsy, progressive myoclonic 3, with or without intracellular inclusions (EPM3)
  • 亞細胞定位:
    Cell membrane. Cytoplasm, cytosol.
  • 數據庫鏈接:

    HGNC: 21957

    OMIM: 611725

    KEGG: hsa:154881

    UniGene: Hs.546627



主站蜘蛛池模板: 欧洲人免费视频网站在线| 国产精品久人妻精品老妇 | 又粗又黄又硬又爽的免费视频| 影音先锋中文字幕人妻| 免费国产在线一区二区| 日韩精品极品视频在线观看免费 | 久久综合九色综合97欧美| 亚洲一二区制服无码中字| 国产在线精品一区二区在线看| 人妻少妇被粗大爽9797pw| 越南毛茸茸的少妇| 乱无码伦视频在线观看| 国产精品国产成人国产三级| 精品av无码国产一区二区| 国产亚洲精品成人aa片| 亚洲色大成网站www永久在线观看 亚洲日韩国产精品无码av | 蜜臀av在线播放一区二区三区| 中文无码日韩欧免费视频| 被窝影院午夜无码国产| 在线综合亚洲欧美网站| 国产sm主人调教女m视频| 内射囯产旡码丰满少妇| 国产精品久久香蕉免费播放| 天天做天天爱夜夜爽| 1000部拍拍拍18勿入免费视频下载| 在线a久青草视频在线观看| 狠狠躁夜夜躁人人爽天天bl| 无遮挡激情视频国产在线观看| 久久九九av免费精品| 动漫av纯肉无码av在线播放| 日本精品人妻无码免费大全| 成人亚洲欧美激情在线电影| 国产97人妻人人做人碰人人爽 | 久久久久免费看黄a片app| 国产 中文 制服丝袜 另类| 亚洲国产精品久久久久爰| 国产情侣真实54分钟在线| 狂野av人人澡人人添| 国产激情久久久久久熟女老人av | 一本一道久久a久久精品综合| 午夜亚洲精品久久一区二区|