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. KY Antibody, FITC conjugated

KY Antibody, FITC conjugated

  • 中文名稱：
    KY兔多克隆抗體, FITC偶聯
  • 貨號：
    CSB-PA012702LC01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) KY Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    KY
  • 別名：
    KY antibody; KY_HUMAN antibody; Kyphoscoliosis peptidase antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Kyphoscoliosis peptidase protein (23-170AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    FITC
  • 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
  • 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：
    Probable cytoskeleton-associated protease required for normal muscle growth. Involved in function, maturation and stabilization of the neuromuscular junction. May act by cleaving muscle-specific proteins such as FLNC.
  • 基因功能參考文獻：
    1. This study shown Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defects in two bother. PMID: 27484770
    2. Homozygous KY mutation was identified as a cause of progressive hereditary spastic paraplegia. High KY transcript levels were demonstrated in muscular organs and lower expression in the CNS. PMID: 28488683
    3. Homozygous c.1071delG, p.(Thr358Leufs*3) variant of KY causes neuromuscular disorder by introducing a premature stop codon. PMID: 27485408
    4. KY expression is significantly downregulated in human masticatory mucosa during wound healing PMID: 28005267
    5. Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) PMID: 20379614

    顯示更多

    收起更多

  • 相關疾病：
    Myopathy, myofibrillar, 7 (MFM7)
  • 亞細胞定位：
    Cytoplasm, cytoskeleton. Cytoplasm, myofibril, sarcomere, Z line.
  • 蛋白家族：
    Transglutaminase-like superfamily
  • 組織特異性：
    Highly expressed in skeletal muscle.
  • 數據庫鏈接：

    HGNC: 26576

    OMIM: 605739

    KEGG: hsa:339855

    STRING: 9606.ENSP00000397598

    UniGene: Hs.146730



主站蜘蛛池模板： 亚洲乱码中文字幕综合| 无码人妻一区二区三区一| 国产在线 | 欧洲| 熟妇人妻午夜寂寞影院| 无翼乌工口全彩肉肉无遮挡18 | 亚洲暴爽av人人爽日日碰| 人人妻人人澡人人爽偷拍台湾| 精品乱码一区二区三四五区| 午夜理论片yy6080私人影院 | 国产av精国产传媒| 国产素人在线观看人成视频| 国产精品夜夜春夜夜爽久久| 天天综合色天天综合色hd| 男女无遮挡激情视频| 在线视频免费观看爽爽爽| 中文人妻av久久人妻18| 久久视频这里只精品99| 97精品尹人久久大香线蕉| 欧美三级a做爰在线观看| 国产精品亚洲欧美大片在线看| 国产成人午夜福利在线观看| 亚洲精品无码人妻无码| 四库影院永久四虎精品国产| 精品久久人人爽天天玩人人妻| 小箩莉末发育娇小性色xxxx| 国内精品免费久久久久软件| 久久不见久久见免费视频1′| 拍真实国产伦偷精品| 久久精品国产大片免费观看| 精品亚洲国产成人av在线时间短的 | 午夜无码乱码在线观看| 免费国产午夜理论片不卡| 国产福利在线永久视频| 国产成人av一区二区三区在线观看 | 亚洲性猛交xxxx| 久久99成人免费| 无码熟熟妇丰满人妻啪啪| 亚洲乱码中文字幕小综合| 欧美老妇与zozoz0交| 欧美性猛交xxxx富婆| 精品一区二区三区国产在线观看|