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. PIGT Antibody

PIGT Antibody

  • 中文名稱：
    PIGT兔多克隆抗體
  • 貨號：
    CSB-PA017983GA01HU
  • 規(guī)格：
    ￥3,900
  • 其他：

產(chǎn)品詳情

  • Uniprot No.：
  • 基因名：
    PIGT
  • 別名：
    PIGT antibody; CGI-06 antibody; PSEC0163 antibody; UNQ716/PRO1379 antibody; GPI transamidase component PIG-T antibody; Phosphatidylinositol-glycan biosynthesis class T protein antibody
  • 宿主：
    Rabbit
  • 反應(yīng)種屬：
    Human,Mouse,Rat
  • 免疫原：
    Human PIGT
  • 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 0.02% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
  • 產(chǎn)品提供形式：
    Liquid
  • 應(yīng)用范圍：
    ELISA,WB,IHC
  • Protocols：
  • 儲(chǔ)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(chǎn)品評價(jià)

靶點(diǎn)詳情

  • 功能：
    Component of the GPI transamidase complex. Essential for transfer of GPI to proteins, particularly for formation of carbonyl intermediates.
  • 基因功能參考文獻(xiàn)：
    1. Whole-exome sequencing revealed compound heterozygous mutations (c.250G > T, p.Glu84X and c.1096G > T, p.Gly366Trp) in PIGT (NM_015937.5), which were confirmed using Sanger sequencing. Thus inherited GPI anchor deficiency associated with these PIGT mutations was diagnosed PMID: 28728837
    2. PIGT-knockout HEK293 cells showed that p.(E237Q) results in a small reduction in the amount of CD59 anchored to the cell membrane. PMID: 28327575
    3. mutations in PIGT as the cause of a novel autosomal recessive intellectual disability syndrome PMID: 23636107
    4. Germline mutation and a somatic mutation in PIGT is associated with paroxysmal nocturnal hemoglobinuria. PMID: 23733340
    5. ER-localized because of information in its transmembrane span PMID: 15713669

    顯示更多

    收起更多

  • 相關(guān)疾病：
    Multiple congenital anomalies-hypotonia-seizures syndrome 3 (MCAHS3); Paroxysmal nocturnal hemoglobinuria 2 (PNH2)
  • 亞細(xì)胞定位：
    Endoplasmic reticulum membrane; Single-pass type I membrane protein.
  • 蛋白家族：
    PIGT family
  • 數(shù)據(jù)庫鏈接：

    HGNC: 14938

    OMIM: 610272

    KEGG: hsa:51604

    STRING: 9606.ENSP00000279036

    UniGene: Hs.437388



主站蜘蛛池模板： 精品成在人线av无码免费看| 欲求不满邻居的爆乳在线播放| 亚洲欧美日韩国产综合v| 国产福利男女xx00视频| 欧美影视精品久久| 国产精品人妻在线观看| 久久人妻av中文字幕| 无码中文字幕在线播放2| 996久久国产精品线观看| 无码精品久久久久久人妻中字| 久九九精品免费视频| 亚洲欧美国产免费综合视频| 性高朝久久久久久久| 在线播放无码高潮的视频| 国产精品99久久不卡| 肉感饱满中年熟妇日本| 国产传媒麻豆剧精品av| 色综合伊人色综合网站无码| 特级做a爰片毛片免费69| 熟睡人妻被讨厌的公侵犯深田咏美| 2020每日更新国产精品视频| 亚洲国产av无码综合原创国产| 久久精品国产网红主播| 中文在线а√天堂| 成人爽a毛片免费网站| 成在人线av无码免费看网站| 在教室伦流澡到高潮hgl视频| 欧洲熟妇色xxxxx欧美老妇伦 | 国产午夜福利精品久久2021| 老熟女 露脸 嗷嗷叫| 性色a∨人人爽网站hdkp885| 日韩国产精品人妻无码久久久| 欧美午夜刺激影院| 日韩精品人妻系列无码专区免费| 成年日韩片av在线网站| 国产欧美日韩亚洲精品专区| 久久久精品人妻一区二区三区四 | 久久人人爽人人爽人人爽| 国产真实偷乱视频| 久久综合色老色| 午夜福利视频|