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. TGDS Antibody, Biotin conjugated

TGDS Antibody, Biotin conjugated

  • 中文名稱：
    TGDS兔多克隆抗體, Biotin偶聯
  • 貨號：
    CSB-PA023444LD01HU
  • 規格：
    ￥880
  • 其他：

產品詳情

  • 產品名稱：
    Rabbit anti-Homo sapiens (Human) TGDS Polyclonal antibody
  • Uniprot No.：
  • 基因名：
    TGDS
  • 別名：
    6-dehydratase antibody; dTDP D glucose 4,6 dehydratase antibody; dTDP-D-glucose 4 antibody; Growth inhibiting protein 21 antibody; SDR2E1 antibody; TDP glucose 4,6 dehydratase antibody; TDPGD antibody; TGDS antibody; TGDS_HUMAN antibody
  • 宿主：
    Rabbit
  • 反應種屬：
    Human
  • 免疫原：
    Recombinant Human dTDP-D-glucose 4,6-dehydratase protein (143-305AA)
  • 免疫原種屬：
    Homo sapiens (Human)
  • 標記方式：
    Biotin
  • 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
  • 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

  • 基因功能參考文獻：
    1. Our findings widen the phenotype spectrum caused by TGDS mutations and underline the phenotypic overlap with Temtamy preaxial brachydactyly syndrome. This improves our understanding of the prenatal development and the pathogenetic mechanism of Catel-Manzke syndrome. PMID: 28422407
    2. By using haplotype reconstruction we showed that the mutation c.298G>T is probably a founder mutation. Due to the spectrum of the amino acid changes, we suggest that loss of function in TGDS is the underlying mechanism of Catel-Manzke syndrome. PMID: 25480037
  • 相關疾病：
    Catel-Manzke syndrome (CATMANS)
  • 蛋白家族：
    NAD(P)-dependent epimerase/dehydratase family, dTDP-glucose dehydratase subfamily
  • 數據庫鏈接：

    HGNC: 20324

    OMIM: 616145

    KEGG: hsa:23483

    STRING: 9606.ENSP00000261296

    UniGene: Hs.12393



主站蜘蛛池模板： 成人麻豆日韩在无码视频| 欧美成人片一区二区三区| 中文在线а天堂中文在线新版| 欧美亅性猛交内射| 天天综合网亚在线| 伊人久久精品无码二区麻豆 | 欧美成人无码a区视频在线观看| 巨人精品福利官方导航| 国产精品女同一区二区| 色欲av亚洲情无码av蜜桃| 久久人人97超碰caoporen| 中文字幕人妻无码系列第三区| 极品尤物被啪到呻吟喷水| 69成人免费视频无码专区| 野花社区免费观看在线www| 无码国产精品一区二区色情男同| 波多野42部无码喷潮| 成人网站色52色在线观看| 日韩免费无码专区精品观看| 97色偷偷色噜噜狠狠爱网站| 国产日产欧产精品精品| 无码av在线一本无码| 久久久久久久久毛片精品| 大伊香蕉精品视频在线天堂| 又湿又黄裸乳漫画无遮挡网站| 老熟女老太婆爽| 99久久久无码国产精品6| 日产幕无线码三区在线| 中文资源在线天堂库8| 亚洲视频一区| 色屁屁www影院免费观看入口 | 国产未成女一区二区| 天天鲁一鲁摸一摸爽一爽| 日日鲁鲁鲁夜夜爽爽狠狠 | 成人伊人亚洲人综合网| 久久午夜羞羞影院免费观看 | 扒开双腿疯狂进出爽爽爽| 一线二线无人区乱码 | 国产成人精品一区二区三区免费看| 亚洲精品无码ma在线观看| 男女啪啪永久免费观看网站|