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

KCTD7 Antibody

  • 中文名稱：
    KCTD7兔多克隆抗體
  • 貨號：
    CSB-PA941590
  • 規格：
    ￥1090
  • 圖片：
    • Western Blot analysis of 1,mouse-brain 2,mouse-spleen cells using primary antibody diluted at 1:1000(4°C overnight). Secondary antibody:Goat Anti-rabbit IgG IRDye 800( diluted at 1:5000, 25°C, 1 hour)
  • 其他：

產品詳情

  • 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,Mouse,Rat
  • 免疫原：
    Synthesized peptide derived from Human KCTD7. at AA range: 181-230
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    Non-conjugated
  • 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.
  • 保存緩沖液：
    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • 產品提供形式：
    Liquid
  • 應用范圍：
    WB,ELISA
  • 推薦稀釋比：
    Application Recommended Dilution
    WB 1:500-2000
    ELISA 1:10000-20000
  • 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

  • 相關疾病：
    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： 2022久久国产精品免费热麻豆| 国产老熟女伦老熟妇露脸| 57pao成人国产永久免费视频| 国产女人高潮视频在线观看| 亚洲熟妇av午夜无码不卡| 2021精品亚洲中文字幕| 精品乱人伦一区二区三区| 又粗又大又硬又长又爽| 中文乱码人妻系列一区| 国产精品一区二区手机在线观看| 在线 v亚洲 v欧美v 专区| 国产成人精品一区二区在线小狼| 日日碰狠狠躁久久躁96avv| 午夜精品久久久久久久四虎| 日韩欧美国产aⅴ另类| 国内自拍视频一区二区三区| 无码av免费毛片一区二区| 岛国4k人妻一区二区三区| 强 暴 疼 哭 处 女 身子视频| 中文字幕在线播放| 免费无码国产v片在线观看| 污18禁污色黄网站免费| 久久久国产精品无码一区二区 | 久久天天躁狠狠躁夜夜躁2014 | 天天躁日日躁aaaxxⅹ| 国产精华av午夜在线| 一本大道无码日韩精品影视丶| 日本无遮挡真人祼交视频| 久久人人爽人人爽爽久久小说| 性做久久久久久久免费看| 国产精品毛片一区二区| 人妻精品制服丝袜久久久| 日本少妇xxxx做受| 国产欧美日韩va另类在线播放| 狠狠狠狼鲁亚洲综合网| 亚洲欧洲av一区二区久久| 成人网站国产在线视频内射视频| 2024av天堂手机在线观看| 精品国际久久久久999| 一本色道久久综合狠狠躁篇| 热99re久久精品这里都是精品|