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： 99久久精品免费看国产一区二区三区| 久久久久国色av免费观看性色| 精品无码国产av一区二区三区| 人妻少妇一区二区三区| 国产天堂久久天堂av色综合| 中文在线а√在线天堂中文| 无遮挡男女激烈动态图| 好硬好湿好爽再深一点动态图视频 | 激情久久亚洲小说| 国产精品人妻在线观看 | 国产无遮挡裸体免费视频| 免费视频成人片在线观看| 亚洲精品无码鲁网中文电影| 亚洲国产果冻传媒av在线观看| 尤物yw193无码点击进入| 精品国产国语对白久久免费 | 麻豆av字幕无码中文| 亚洲色欲色欲综合网站| 亚洲欧美国产精品久久| 777精品久无码人妻蜜桃| 天堂在线最新版www中文| 中文字幕亚洲一区二区三区| 久久欧美与黑人双交男男| 综合久久国产九一剧情麻豆| 国内野外强奷在线视频| 又色又爽又高潮免费视频观看| 亚洲永久网址在线观看| 欧美日本亚洲韩国一区| 亚洲va在线∨a天堂va欧美va| 国精产品一二三区传媒公司| 天天天天做夜夜夜夜做无码| 邪恶肉肉全彩色无遮盖| 无码丰满熟妇juliaann与黑人| 亚洲第一网站男人都懂| 欧美影视精品久久| 欧美寡妇xxxx黑人猛交| 成在人线av无码免观看午夜网 | 亚洲女女女同性video| 人妻.中文字幕无码| 无套中出丰满人妻无码| 性生交大片免费看l|