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. ROGDI Antibody, FITC conjugated

ROGDI Antibody, FITC conjugated

  • 中文名稱：
    ROGDI兔多克隆抗體, FITC偶聯
  • 貨號：
    CSB-PA867108LC01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) ROGDI Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    ROGDI
  • 別名：
    FLJ22386 antibody; KTZS antibody; Leucine zipper domain protein antibody; Protein rogdi homolog antibody; rogdi antibody; rogdi homolog (Drosophila) antibody; rogdi, Drosophila, homolog of antibody; ROGDI_HUMAN antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human Protein rogdi homolog protein (14-287AA)
  • 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：
    Antigen Affinity 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

  • 基因功能參考文獻：
    1. We identify novel compound heterozygous ROGDI mutations in five typical Kohlschutter-Tonz syndrome families. Other families were negative for ROGDI mutations, suggesting genetic heterogeneity of atypical forms of the disease. PMID: 23086778
    2. The finding that ROGDI mutations cause Kohlschutter-Tonz Syndrome indicates that the protein product of this gene plays an important role in neuronal development as well as amelogenesis. PMID: 22424600
    3. Homozygosity mapping localized the gene linked to Kohlschutter-Tonz syndrome to a 586,513 bp region (with a LOD score of 6.4) in chromosomal region 16p13.3. The nonsense mutation was homozygous in all affected individuals. PMID: 22482807
  • 相關疾病：
    Kohlschuetter-Toenz syndrome (KTZS)
  • 亞細胞定位：
    Nucleus envelope. Cell junction, synapse, presynapse. Cell projection, axon. Perikaryon. Cell projection, dendrite. Cytoplasmic vesicle, secretory vesicle, synaptic vesicle.
  • 蛋白家族：
    Rogdi family
  • 組織特異性：
    Widely expressed with highest levels in spinal cord, brain, heart and bone marrow. Also expressed in fetal brain and liver.
  • 數據庫鏈接：

    HGNC: 29478

    OMIM: 226750

    KEGG: hsa:79641

    UniGene: Hs.459795



主站蜘蛛池模板： 国产杨幂丝袜av在线播放| 久久精品欧美日韩精品| 国产偷伦视频片免费视频| 国产卡一卡二卡三卡免费| 十八禁av无码免费网站| 高中生自慰www网站| 国产美女被遭高潮免费视频| 欧美综合乱图图区乱图图区| 中文国产成人精品久久app | 国产精品丝袜黑色高跟鞋| 久久综合久久鬼色| 久久精品国产999久久久| 色屁屁www影院免费观看| 亚洲精品乱码久久久久久久久久久久 | 少妇无码av无码去区钱| 性欧美vr高清极品| 国产肉体xxxx裸体137大胆| 国产原创av中文在线观看| 玩两个丰满老熟女久久网| 国产真实乱对白精彩久久老熟妇女| 人妻少妇久久中文字幕456| 精品无人乱码高清| 亚洲精品午夜国产va久久成人| 日韩成av人片在线观看| 五月婷婷激情第四季| 欲色欲色天天天www| 精品无码国产一区二区三区麻豆| 久久久久国精品产熟女久色| 性av盈盈无码天堂| 中文字幕亚洲欧美在线不卡| 国产h视频在线观看| 成人av在线一区二区三区| 2019最新中文字幕在线观看| 国产成人一区二区三区影院动漫| 亚洲久热中文字幕在线| 图片区小说区另类春色| www一区二区www免费| 色综合色欲色综合色综合色综合r| 少妇被粗大的猛烈进出动视频| 久久人妻av中文字幕| 国产欧美日韩专区发布|