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. 首頁
  2. 蛋白
  3. 重組蛋白
  4. Recombinant Human Beta-1,3-glucosyltransferase (B3GALTL), partial

Recombinant Human Beta-1,3-glucosyltransferase (B3GALTL), partial

  • 中文名稱：
    Recombinant Human Beta-1,3-glucosyltransferase(B3GALTL),partial
  • 貨號：
    CSB-YP754479HU
  • 說明書：
  • 規格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    Recombinant Human Beta-1,3-glucosyltransferase(B3GALTL),partial
  • 貨號：
    CSB-EP754479HU
  • 說明書：
  • 規格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    Recombinant Human Beta-1,3-glucosyltransferase(B3GALTL),partial
  • 貨號：
    CSB-EP754479HU-B
  • 說明書：
  • 規格：
  • 來源：
    E.coli
  • 共軛：
    Avi-tag Biotinylated

    E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag.

  • 其他：
  • 中文名稱：
    Recombinant Human Beta-1,3-glucosyltransferase(B3GALTL),partial
  • 貨號：
    CSB-BP754479HU
  • 說明書：
  • 規格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    Recombinant Human Beta-1,3-glucosyltransferase(B3GALTL),partial
  • 貨號：
    CSB-MP754479HU
  • 說明書：
  • 規格：
  • 來源：
    Mammalian cell
  • 其他：

產品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
    B3GLCT
  • Uniprot No.：
  • 別名：
    B3GLCT; B3GALTL; B3GTLBeta-1,3-glucosyltransferase; Beta3Glc-T; EC 2.4.1.-; Beta 3-glucosyltransferase; Beta-3-glycosyltransferase-like
  • 種屬：
    Homo sapiens (Human)
  • 蛋白長度：
    Partial
  • 蛋白標簽：
    Tag?type?will?be?determined?during?the?manufacturing?process.
    The tag type will be determined during production process. If you have specified tag type, please tell us and we will develop the specified tag preferentially.
  • 產品提供形式：
    Lyophilized powder Warning: in_array() expects parameter 2 to be array, null given in /www/web/cusabio_cn/public_html/caches/caches_template/default/content/show_product_protein.php on line 662
    Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.
  • 復溶：
    We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
  • 儲存條件：
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質期：
    The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
    Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.
  • 貨期：
    Delivery time may differ from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
    Note: All of our proteins are default shipped with normal blue ice packs, if you request to ship with dry ice, please communicate with us in advance and extra fees will be charged.
  • 注意事項：
    Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.
  • Datasheet ：
    Please contact us to get it.

產品評價

靶點詳情

  • 功能：
    O-glucosyltransferase that transfers glucose toward fucose with a beta-1,3 linkage. Specifically glucosylates O-linked fucosylglycan on TSP type-1 domains of proteins, thereby contributing to elongation of O-fucosylglycan.
  • 基因功能參考文獻：
    1. Studies indicate that Peters Plus syndrome is caused by mutations in beta 3-glucosyltransferase (B3GALTL). PMID: 27049305
    2. POFUT2 and B3GLCT mediate a noncanonical endoplasmic reticulum quality-control mechanism that recognizes folded thrombospondin type 1 repeats and stabilizes them by glycosylation. PMID: 25544610
    3. Mutations in the coding region of B3GALTL were identified in nine patients; six had a documented phenotype of classic Peters plus syndrome (PPS) and the remaining three had a clinical diagnosis of PPS with incomplete clinical documentation. PMID: 23889335
    4. a novel c.597-2 A>G splicing mutation within the B3GALTL gene in typical Peters-plus syndrome PMID: 23954224
    5. A novel homozygous c.597-2A>G mutation was identified in both patients with Peters plus syndrome harbouring a novel splice site mutation in the B3GALTL gene PMID: 22759511
    6. Vertebral defects in a patient with Peters plus syndrome and mutations in B3GALTL. PMID: 21671750
    7. The present report confirms the wide clinical spectrum of Peters plus syndrome, underlines the major clinical criteria of the syndrome and the major implication of B3GALTL gene in this condition. PMID: 21067481
    8. Novel B3GALTL mutation in Peters-plus Syndrome PMID: 19796186
    9. B3GTL is transcribed in a wide range of tissues and has conserved domains and motifs PMID: 12943678
    10. We report here the molecular cloning and characterization of a novel beta1,3-glucosyltransferase (beta3Glc-T) that synthesizes a Glcbeta1,3Fucalpha- structure on the TSR domain. PMID: 16899492
    11. Biallelic truncating mutations in the beta 1,3-galactosyltransferase-like gene (B3GALTL) in all 20 tested patients, showed that Peters Plus is a monogenic, primarily single-mutation syndrome. PMID: 16909395
    12. Peters Plus syndrome is a new congenital disorder of glycosylation and involves defective Omicron-glycosylation of thrombospondin type 1 repeats.( PMID: 18199743
    13. two new mutant alleles, c.459 + 1G > A and c.230insT, were identified and predicted to result in truncated protein products; data confirm an important role for B3GALTL in causing typical Peters Plus syndrome PMID: 18798333

    顯示更多

    收起更多

  • 相關疾病：
    Peters-plus syndrome (PPLS)
  • 亞細胞定位：
    Endoplasmic reticulum membrane; Single-pass type II membrane protein.
  • 蛋白家族：
    Glycosyltransferase 31 family
  • 組織特異性：
    Widely expressed, with highest levels in testis and uterus.
  • 數據庫鏈接：

    HGNC: 20207

    OMIM: 261540

    KEGG: hsa:145173

    STRING: 9606.ENSP00000343002

    UniGene: Hs.13205



主站蜘蛛池模板： 动漫av一区二区在线观看| 亚洲精品一区二区三区不卡| 疯狂做受xxxx高潮不断| 成人一区二区免费中文字幕视频 | 黄床片30分钟免费视频教程| 亚洲一区av无码专区在线观看| 久久99热狠狠色精品一区| 刺激一区仑乱| 国产免费一卡二卡三卡四卡| 国语对白刺激精品视频| 先锋影音男人av资源| 日本最新免费二区三区| 欧美亚洲日韩国产综合电影 | 国产作爱激烈叫床视频| 艳妇臀荡乳欲伦交换h在线观看| 人妻换人妻仑乱| 久久久亚洲欧洲日产无码av| 日韩亚洲国产激情一区浪潮av| 亚洲色偷拍另类无码专区| 色综合久久久久综合体桃花网| 免费观看在线a毛片| 国产交换配偶在线视频| 人妻少妇中文字幕久久| 亚洲的天堂av无码| 国产亚洲精品久久久久久国| 国产午夜福利在线观看视频_| 欧美伊人久久大香线蕉综合| 四川少妇被弄到高潮| 人妻出轨av中文字幕| 日本 精品 高清不卡| 久久综合九色综合欧美98| 无码人妻精品一区二区三区不卡| 精品久久国产综合婷婷五月| 久久这里有精品国产电影网| 乱女伦露脸对白在线播放| 夜色福利院在线观看免费| 天堂网www最新版官网| 波多野结衣人妻| 亚洲精品字幕| 亚洲精品入口一区二区乱麻豆精品 | 99精品国产丝袜在线拍国语|