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: 成人亚洲欧美丁香在线观看| 天天av天天爽无码中文| 无码人妻丰满熟妇区免费| 亚洲国产最大av| 国产欧美另类久久久精品丝瓜| 狠狠亚洲狠狠欧洲2019| 国产精品区av| 亚洲精品456在线播放| 熟女人妻aⅴ一区二区三区麻豆| 久久午夜私人影院| 亚洲国产成人爱av网站| 国产精品偷窥熟女精品视频| 日本亚洲色大成网站www| 欧美肥婆性猛交xxxx| a级大胆欧美人体大胆666| 国产午夜片无码区在线观看| 日日噜噜夜夜狠狠va视频v| 吃奶呻吟打开双腿做受在线视频| 成年女人永久免费看片| 无码精品国产d在线观看| 天堂8在线新版官网| 欧洲美熟女乱又伦av影片| 色丁狠狠桃花久久综合网| 无码精品国产d在线观看| 亚洲色成人网一二三区| 久久久久99人妻一区二区三区 | 麻豆一区二区三区精品视频| 国产又色又爽又黄好看的视频| 男女做爰猛烈啪啪吃奶动| 中文无码天天av天天爽| 欧美老熟妇乱大交xxxxx| 色综合欧美亚洲国产| 亚洲国产码专区| 欧美丰满熟妇xxxx性大屁股| 精品人妻无码一区二区三区抖音| 中文字幕在线亚洲日韩6页| 亚洲 欧洲 日韩 综合av| 天堂在线观看www| 高清不卡毛片免费观看| 精品国产午夜福利精品推荐| 最近免费中文字幕mv在线视频3|