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. KCTD7 Antibody, HRP conjugated

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： 成人午夜无码精品免费看| 国模裸体无码xxxx视频| 欧美v亚洲v日韩v最新在线| 麻豆av传媒蜜桃天美传媒| 亚洲欧美日本中文字不卡| 波多野结衣一区二区三区av免费 | 成人黄网站高清免费视频| 国产亚洲欧美精品永久| 精品一区二区不卡无码av| 韩国精品无码少妇在线观看| 色婷婷亚洲精品综合影院| 99久久免费国产精精品| 欧美日韩在线第一页免费观看| 久久伊人精品波多野结衣| 欧美激烈精交gif动态图| 亚洲成a人片在线观看天堂无码| 在线看免费无码av天堂| 国产精成人品| 日本一卡2卡3卡4卡免费精品| 欧美另类人妖| 西西人体www大胆高清| 四虎永久免费地址入口| 久久久肥妇熟女ⅹxxx毛片| 国产成人av男人的天堂| 精品久久久无码中文字幕边打电话| 丝袜无码专区人妻视频| 久久热最新网站获取| 秋霞影院午夜伦a片欧美| 无码国产乱人伦偷精品视频| 女m羞辱调教视频网站| 精品综合久久久久久8888| 超碰人人超碰人人| 看黄a大片爽爽影院免费无码| 国产亚洲久久久久久久| 亚洲aⅴ综合av国产八av| 精品国偷自产在线| 午夜裸体性播放| 国产免费又色又爽又黄软件| 伦埋琪琪久久影院三级| 人妻有码av中文字幕久久琪| 久久九九兔免费精品6|