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： 精品亚洲国产成人av制服| 女人被做到高潮免费视频| 性欧美俄罗斯极品| 成人av片在线观看免费| 狠狠躁天天躁中文字幕无码| 欧洲精品码一区二区三区| 天天躁日日躁狠狠躁2018| 在线视频免费无码专区| 精品久久久无码中文字幕天天| 狠狠综合久久av一区二区| 国产欧美va欧美va香蕉在线观看| 天天综合网亚在线| 337p日本欧洲亚洲大胆精品| 亚洲午夜无码av毛片久久| 日本丰满熟妇videossex| 狂野欧美激情性xxxx在线观看 | 狠狠色噜噜狠狠狠狠777米奇| 亚洲综合av色婷婷五月蜜臀| 成人a毛片视频免费看| 欧美精品国产综合久久| 国产人成视频在线视频| 久久久久青草线蕉亚洲麻豆| 亚洲愉拍自拍另类图片 | 4438xx亚洲最大五色丁香| 日本一区二区a√成人片| 亚洲国产成人精品无码区一本 | 午夜亚洲www湿好大| 亚洲精品中文字幕乱码4区| 噜噜噜亚洲色成人网站∨| 亚洲无人区码一码二码三码的含义| 国产精品久久久久久无码五月| 97se色综合一区二区二区| 酒店大战丝袜高跟鞋人妻| 色欲久久人妻内射| 99亚洲精品自拍av成人| 美女无遮挡免费视频网站| 国产亚洲视频在线观看播放| 少妇无码av无码专区线y| 国产欧美在线观看不卡| 久久久久香蕉国产线看观看伊| 麻豆国产原创视频在线播放|