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

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: 午夜免费啪视频在线观看区| 久久只有这里有精品4| 五十路熟妇强烈无码| 图片区小说区av区| 精品国产成人高清在线观看| 欧美黑人巨大videos精品| 日韩精品一区二区三区在线观看| 国产精品爽爽久久久久久| 久久久综合亚洲色一区二区三区| 精品无码一区二区三区爱欲| 国产福利萌白酱精品tv一区| 亚洲男人片片在线观看| 最新亚洲中文av在线不卡| 日本少妇被黑人猛cao| 国产92成人精品视频免费| 嫩b人妻精品一区二区三区| 亚洲中文字幕永久在线不卡| 国产精品一区二区手机在线观看| 欧美另类 自拍 亚洲 图区| 精品国产乱码一区二区三区| 亚洲狠狠婷婷综合久久蜜芽| 人人做人人妻人人精| 动漫av永久无码精品每日更新| 一本无码中文字幕在线观| 蜜臀avwww国产天堂| 久久精品中文字幕一区| 日韩中文字幕在线一区二区三区 | 日本va在线视频播放| 久在线观看福利视频| 丰满饥渴老女人hd| 日本高清www午色夜在线视频| 免费无码又爽又刺激成人| 377p欧洲日本亚洲大胆| 无码福利日韩神码福利片 | 国产色诱视频在线观看| 国产在线一区二区在线视频| 久久精品亚洲综合专区| 中文字幕精品久久久久人妻| 亚洲国产精品综合久久网络| 人妻丰满熟妇av无码片| 国产精品亚洲二区在线看|