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： 中文字幕久久综合伊人| 久久久国产精品va麻豆| 亚洲kkk4444在线观看| 精品国产电影久久九九| 一区二区三区av高清免费波多| 精品国模一区二区三区| 成熟人妻av无码专区| 男女性杂交内射妇女bbwxz| 亚洲va天堂va欧美片a在线| 国产精品女主播在线视频| 亚洲欧洲国产成人综合在线观看| 色窝窝免费一区二区三区| 少妇厨房愉情理9仑片视频| 丰满护士巨好爽好大乳| 色欲来吧来吧天天综合网| 人体内射精一区二区三区| 高潮毛片无遮挡高清免费| 欧美一性一乱一交一视频| 久99视频精品免费观看福利| 国产又色又爽又黄的在线观看| 免费人成激情视频在线观看冫| 一个人在线观看免费中文www | 日韩亚洲国产综合高清 | 少妇人妻中文字幕污| 国产av无码专区亚洲版综合| 中文字幕丰满乱子伦无码专区| 国产成a人亚洲精v品无码| 免费无码成人av电影在线播放| 日韩人妻少妇一区二区三区 | 一 级 黄 色 片免费网站| 午夜福利国产成人无码gif动图| 8ⅹ8x擦拨擦拨成人免费视频| 国产亚洲精aa在线观看| 免费无码又爽又高潮视频| 无码少妇一区二区三区芒果| 国产婷婷亚洲999精品小说| 欧美人禽zozo动人物杂交| 色妺妺在线视频| 成人3d动漫一区二区三区| av区无码字幕中文色| 国产精品久久久久久52avav|