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. IFT172 Antibody, FITC conjugated

IFT172 Antibody, FITC conjugated

  • 中文名稱：
    IFT172兔多克隆抗體, FITC偶聯
  • 貨號：
    CSB-PA887019LC01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) IFT172 Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    IFT172
  • 別名：
    IF172_HUMAN antibody; ift172 antibody; Intraflagellar transport 172 homolog (Chlamydomonas) antibody; Intraflagellar transport protein 172 homolog antibody; Osm 1 antibody; Selective LIM binding factor homolog antibody; SLB antibody; Wim antibody; Wimple homolog antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Intraflagellar transport protein 172 homolog protein (1368-1502AA)
  • 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：
    Required for the maintenance and formation of cilia. Plays an indirect role in hedgehog (Hh) signaling, cilia being required for all activity of the hedgehog pathway.
  • 基因功能參考文獻：
    1. This is the second report of IFT172 mutations in BBS patients validating IFT172 as the twentieth BBS gene (BBS20). PMID: 26763875
    2. Findings identified mutations in IFT172 that lead to a recessive form of non-syndromic retinitis pigmentosa and Bardet-Biedl syndrome and suggest that the primary IFT172 mutations alone are not sufficient to explain the wide range of phenotypes. PMID: 25168386
    3. We have identified defects in IFT172 as a cause of complex asphyxiating thoracic dystrophy and Mainzer-Saldino syndrome. PMID: 24140113
  • 相關疾病：
    Short-rib thoracic dysplasia 10 with or without polydactyly (SRTD10); Retinitis pigmentosa 71 (RP71)
  • 亞細胞定位：
    Cell projection, cilium. Note=Localized to the axoneme and around the base of the cilium.
  • 蛋白家族：
    IFT172 family
  • 數據庫鏈接：

    HGNC: 30391

    OMIM: 607386

    KEGG: hsa:26160

    STRING: 9606.ENSP00000260570

    UniGene: Hs.127401



主站蜘蛛池模板： 人妻影音先锋啪啪av资源| 高清乱码一区二区三区| 国产男生夜间福利免费网站| 丰满少妇被猛烈进av毛片| 精品三级久久久久电影网| 大伊香蕉精品视频在线 | 国产真人性做爰久久网站| 强行糟蹋人妻hd中文字| 又黄又爽吃奶视频在线观看| 亚洲人成在线观看网站不卡| 国产精品主播一区二区三区| 欧美精品a∨在线观看| 欧美另类bbbxxxxx另类| 中文天堂资源在线www| 成人精品视频一区二区| 久久久成人精品av四区| 在线综合亚洲欧美网站| 色欲av久久综合人妻无码| 亚洲欧美日韩国产自偷| 成年女人毛片免费视频| 久久综合88熟人妻| 亚洲欧美国产另类va| av无码久久久精品免费| 水蜜桃av导航| 精品福利一区二区三区免费视频| 国产女人高潮视频在线观看| 亚洲综合久久无码色噜噜赖水| 亚洲日韩乱码中文无码蜜桃臀网站| 亚洲成a人v欧美综合天堂麻豆| 无码一区二区三区| 国产成人精品免费视频大全五级| 东北老女人高潮大喊舒服死了 | 不卡高清av手机在线观看| 一卡二卡3卡四卡网站精品| 99久久久无码国产精品不卡| 少妇性l交大片| 看成年全黄大色黄大片| 2021麻豆剧传媒一二三区| 四虎永久在线精品免费网站| 丰满人妻熟妇乱又伦精品视| 国产jjzzjjzz视频全部免费|