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： 偷窥 亚洲 另类 图片 熟女 | 亚洲最大无码av网站观看| 久久精品av一区二区免费| 国产成人理论无码电影网| 国产在线一区二区三区四区五区| 一道久久爱综合久久爱| 乱码av麻豆丝袜熟女系列| 男女又色又爽又爽视频| 亚洲欧美成人综合图区| 亚洲无线码免费| 欧美人禽杂交狂配| 亚洲啪av永久无码精品放毛片| 亚洲深深色噜噜狠狠爱网站| 久久久综合九色综合鬼色| 日韩国产成人无码av毛片蜜柚| 好硬好湿好爽再深一点动态图视频| 人妻无码一区二区三区| 免费人妻精品一区二区三区| 国产α片免费观看在线人| 亚洲精品久久一区二区无卡| 人人添人人澡人人澡人人人人| 亚州av综合色区无码一区| 日韩精品久久久久久久电影蜜臀 | 成人毛片一区二区| 欧美不卡一卡二卡三卡| 免费人成网站在线观看视频| 夜夜爽妓女8888888视频| 毛多水多www偷窥小便| 精品一区二区三区东京热| 久久中文字幕无码中文字幕有码| 中文在线www天堂网| 午夜家庭影院| 国产乡下三级全黄三级bd| 伊人伊成久久人综合网996| 狠狠色噜噜狠狠狠狠五月婷| 国产亚洲视频中文字幕97精品| 人妻精品国产一区二区| 影音先锋无码a∨男人资源站| 久久日本片精品aaaaa国产| 亚洲色偷拍另类无码专区| 5x性社区免费视频播|