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

Recombinant Human DDB1- and CUL4-associated factor 17 (DCAF17), partial

  • 中文名稱:
    Recombinant Human DDB1- and CUL4-associated factor 17(DCAF17),partial
  • 貨號:
    CSB-YP705161HU1
  • 規格:
  • 來源:
    Yeast
  • 其他:
  • 中文名稱:
    Recombinant Human DDB1- and CUL4-associated factor 17(DCAF17),partial
  • 貨號:
    CSB-EP705161HU1
  • 規格:
  • 來源:
    E.coli
  • 其他:
  • 中文名稱:
    Recombinant Human DDB1- and CUL4-associated factor 17(DCAF17),partial
  • 貨號:
    CSB-EP705161HU1-B
  • 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 DDB1- and CUL4-associated factor 17(DCAF17),partial
  • 貨號:
    CSB-BP705161HU1
  • 規格:
  • 來源:
    Baculovirus
  • 其他:
  • 中文名稱:
    Recombinant Human DDB1- and CUL4-associated factor 17(DCAF17),partial
  • 貨號:
    CSB-MP705161HU1
  • 規格:
  • 來源:
    Mammalian cell
  • 其他:

產品詳情

  • 純度:
    >85% (SDS-PAGE)
  • 基因名:
    DCAF17
  • Uniprot No.:
  • 別名:
    DCAF17; C2orf37; DDB1- and CUL4-associated factor 17
  • 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
    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:
    May function as a substrate receptor for CUL4-DDB1 E3 ubiquitin-protein ligase complex.
  • 基因功能參考文獻:
    1. The phenotypic variability of Woodhouse-Sakati syndrome due to c.436delC founder DCAF17 mutation may have a wider range than previously recognized. PMID: 29574468
    2. This signifies the vital yet unexplored role of DCAF17 both in development and maintenance of adult tissues homeostasis. PMID: 26612766
    3. two novel frameshift mutations in C2orf37 present in the compound heterozygous state in an Indian family with Woodhouse-Sakati syndrome, is reported. PMID: 26440089
    4. Direct sequencing of the C2orf37 gene revealed that the c.436delC (p.Ala147Hisfs*9) mutation was present in a homozygous state in all affected siblings and in a heterozygous state in the parents and a healthy sister. PMID: 24015686
    5. The results of this study demonistrated that the syndrome of deafness-dystonia is cause by mutation of DCAF17. PMID: 23418071
    6. Pakistani family with clinical manifestations of Woodhouse-Sakati Syndrome; DNA sequence analysis revealed a novel splice site mutation (c.321 + 1 G > A) in the gene C2orf37, mapped on chromosomes 2q22.3-2q35 PMID: 21963443
    7. Mutations in C2orf37 are responsible for Woodhouse-Sakati syndrome. PMID: 21964978
    8. A novel C2orf37 mutation causes the first Italian cases of Woodhouse Sakati syndrome PMID: 21044051
    9. C2orf37 mutational spectrum in Woodhouse-Sakati syndrome patients PMID: 20507343
    10. Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndrome. PMID: 19026396

    顯示更多

    收起更多

  • 相關疾病:
    Woodhouse-Sakati syndrome (WoSaS)
  • 亞細胞定位:
    Membrane; Multi-pass membrane protein. Nucleus, nucleolus. Note=According to PubMed:19026396, it is a nucleolar protein, while sequence analysis programs clearly predict 2 transmembrane regions.
  • 組織特異性:
    Ubiquitously expressed.
  • 數據庫鏈接:

    HGNC: 25784

    OMIM: 241080

    KEGG: hsa:80067

    STRING: 9606.ENSP00000364404

    UniGene: Hs.659439



主站蜘蛛池模板: 亚洲国产av无码综合原创国产| 国内少妇偷人精品免费| 午夜婷婷精品午夜无码a片影院| 欧美自拍亚洲综合丝袜| 国产色无码精品视频免费 | 亚洲gv天堂gv无码男同| 992tv精品视频tv在线观看| 成人午夜福利视频后入| 亚洲精品国产一区二区| 亚洲国产精品无码久久青草| 中国做爰国产精品视频| 又粗又大又黄又爽的免费视频| 国产无套内射久久久国产| 天堂资源中文最新版在线一区 | 国产精品无码制服丝袜| 国产麻豆精品久久一二三| 免费观看国产小粉嫩喷水| 中文字幕无码家庭乱欲| 国产成人久久精品一区二区三区| 国内精品视频自在一区| 国产精品视频色拍在线视频| 长腿校花无力呻吟娇喘的视频| 色先锋av影音先锋在线| 色www永久免费视频首页| 狂野欧美激情性xxxx按摩| 黑人巨大精品欧美黑寡妇| 久久精品女人天堂av麻| 日本强伦姧人妻久久影片| 最近日本免费观看高清视频 | 香港三日本三级少妇三级2021| 天下第一社区视频www日本| 成人亚洲性情网站www在线观看| 亚洲精品~无码抽插| 亚洲youwu永久无码精品| 亚洲bbw性色大片| 亚洲国产成人综合精品| 久久久欧美精品激情| 欧美 亚洲 日韩 中文2019 | 边添小泬边狠狠躁视频| 人妻avav中文系列久久| 韩国精品视频一区二区在线播放 |