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. ECEL1 Antibody

ECEL1 Antibody

  • 中文名稱：
    ECEL1兔多克隆抗體
  • 貨號：
    CSB-PA007373GA01HU
  • 規格：
    ￥3,900
  • 其他：

產品詳情

  • Uniprot No.：
  • 基因名：
    ECEL1
  • 別名：
    ECEL1; XCE; UNQ2431/PRO4991; Endothelin-converting enzyme-like 1; Xce protein
  • 宿主：
    Rabbit
  • 反應種屬：
    Human,Mouse,Rat
  • 免疫原：
    Human ECEL1
  • 免疫原種屬：
    Homo sapiens (Human)
  • 抗體亞型：
    IgG
  • 純化方式：
    Antigen Affinity purified
  • 濃度：
    It differs from different batches. Please contact us to confirm it.
  • 保存緩沖液：
    PBS with 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 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 contribute to the degradation of peptide hormones and be involved in the inactivation of neuronal peptides.
  • 基因功能參考文獻：
    1. Mutation of a conserved residue in ECEL1 is linked with fetal arthrogryposis multiplex congenita. PMID: 25708584
    2. Our clinical findings are consistent with recessive ECEL1 mutations causing variably penetrant orbital dysinnervation phenotypes (ptosis and/or complex strabismus with abnormal synkinesis) PMID: 25173900
    3. Three novel ECEL1 mutations have been identified in consanguineous pedigrees of Saudi Arabian origin presenting with distal arthrogryposis type 5D. PMID: 23829171
    4. A novel missense c.1819G>A mutation (G607S) in the ECEL1 gene has been identified in a consanguineous pedigree of Turkish origin presenting with congenital contracture syndromes. PMID: 23808592
    5. We described a new and homogenous phenotype of DA associated with ECEL1 that resulted in symptoms involving rather the peripheral than the central nervous system and suggesting a developmental dysfunction PMID: 23236030
    6. Mutations in ECEL1 cause distal arthrogryposis type 5D. PMID: 23261301
    7. Sp1 recruits ATF3, c-Jun, and STAT3 to obtain the requisite synergistic effect in neuronal injury through DINE neuronal injury-inducible gene PMID: 18192274

    顯示更多

    收起更多

  • 相關疾病：
    Arthrogryposis, distal, 5D (DA5D)
  • 亞細胞定位：
    Membrane; Single-pass type II membrane protein.
  • 蛋白家族：
    Peptidase M13 family
  • 組織特異性：
    Highly expressed in the CNS, in particular in putamen, spinal cord, medulla and subthalamic nucleus. A strong signal was also detected in uterine subepithelial cells and around renal blood vessels. Detected at lower levels in amygdala, caudate, thalamus,
  • 數據庫鏈接：

    HGNC: 3147

    OMIM: 605896

    KEGG: hsa:9427

    STRING: 9606.ENSP00000302051

    UniGene: Hs.26880



主站蜘蛛池模板： 精品久久久久久无码人妻热| 亚洲国产色播av在线| 久久久久久久综合狠狠综合| 无码av无码天堂资源网| 久久久综合九色综合88| 国产精品真实灌醉女在线播放| 国产公开免费人成视频| 中出内射颜射骚妇| 人妻免费一区二区三区最新| 同性女女黄h片在线播放| 少妇高潮喷水惨叫久久久久电影| 亚洲乱码国产一区三区| 西西人体大胆4444www| 亚洲春色av无码专区在线播放| 国产午夜高潮熟女精品av软件| 久久久无码一区二区三区| 人人玩人人添人人澡超碰偷拍 | 日本xxxx裸体xxxx视频大全| 韩国三级丰满少妇高潮| 欧美激情乱人伦| 在线观看高清黄网站观看| 久久久国产精品人人片| 欧洲亚洲色一区二区色99| 精品自拍亚洲一区在线| 69堂人成无码免费视频果冻传媒| 伊人久久综合色| 久久777国产线看观看精品| 久久久国产99久久国产久麻豆 | 性无码一区二区三区在线观看| 另类内射国产在线| 一区二区精品视频日本| 在线观看成人无码中文av天堂不卡 | 精品服丝袜无码视频一区| 男人边吃奶边揉好爽免费视频 | 日韩无码专区| 精品国产不卡在线观看免费| 国产欧美精品一区二区色综合| 18禁裸男晨勃露j毛免费观看| 欧美506070老妇乱子伦| 最新中文乱码字字幕在线| 久久精品国产色蜜蜜麻豆|