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 E3 ubiquitin-protein ligase HERC2 (HERC2), partial

Recombinant Human E3 ubiquitin-protein ligase HERC2 (HERC2), partial

  • 中文名稱：
    人HERC2重組蛋白
  • 貨號：
    CSB-YP010293HU
  • 規格：
  • 來源：
    Yeast
  • 其他：
  • 中文名稱：
    人HERC2重組蛋白
  • 貨號：
    CSB-EP010293HU
  • 規格：
  • 來源：
    E.coli
  • 其他：
  • 中文名稱：
    人HERC2重組蛋白
  • 貨號：
    CSB-EP010293HU-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：
    人HERC2重組蛋白
  • 貨號：
    CSB-BP010293HU
  • 規格：
  • 來源：
    Baculovirus
  • 其他：
  • 中文名稱：
    人HERC2重組蛋白
  • 貨號：
    CSB-MP010293HU
  • 規格：
  • 來源：
    Mammalian cell
  • 其他：

產品詳情

  • 純度：
    >85% (SDS-PAGE)
  • 基因名：
  • Uniprot No.：
  • 別名：
    D15F37S1; E3 ubiquitin-protein ligase HERC2; HECT and RLD domain containing E3 ubiquitin protein ligase 2; HECT domain and RCC1 like domain containing protein 2; HECT domain and RCC1-like domain-containing protein 2; Hect domain and RLD 2; HERC2; HERC2_HUMAN; jdf2 ; MRT38; p528 ; Probable E3 ubiquitin-protein ligase HERC2; SHEP1
  • 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：
    E3 ubiquitin-protein ligase that regulates ubiquitin-dependent retention of repair proteins on damaged chromosomes. Recruited to sites of DNA damage in response to ionizing radiation (IR) and facilitates the assembly of UBE2N and RNF8 promoting DNA damage-induced formation of 'Lys-63'-linked ubiquitin chains. Acts as a mediator of binding specificity between UBE2N and RNF8. Involved in the maintenance of RNF168 levels. E3 ubiquitin-protein ligase that promotes the ubiquitination and proteasomal degradation of XPA which influences the circadian oscillation of DNA excision repair activity. By controlling the steady-state expression of the IGF1R receptor, indirectly regulates the insulin-like growth factor receptor signaling pathway.
  • 基因功能參考文獻：
    1. The results of this study are the first to show an association between HERC2 variants and time to first cSCC post-transplant. PMID: 28456133
    2. By downregulating acetylated LKB1 protein via HERC2, SIRT1 fine-tunes the crosstalk between endothelial and vascular smooth muscle cells to prevent adverse arterial remodeling and maintain vascular homeostasis PMID: 27259994
    3. Evaluated the association of seven OCA2-HERC2 SNPs and haplotypes with pigmentation characteristics (eye, skin, hair and freckles) in the highly admixed and phenotypically heterogeneous Brazilian population. Such SNPs and haplotypes could be deemed as good predictors for the presence of freckles and for skin, eye and hair pigmentation in the Brazilian population. PMID: 28081795
    4. SNP rs12913832 in HERC2 was found to be strongly associated with blue eye colour. SNP associations with hair and skin colour were weaker and genotypes less predictive. PMID: 26286644
    5. Data show that histone H2A deubiquitinase USP16 interacts with E3 ubiquitin-protein ligase HERC2, negatively regulates DNA damage-induced ubiquitin foci formation, and is required for termination of the ubiquitin signal. PMID: 25305019
    6. Results identify HERC2 as a regulator of p53 signaling. PMID: 24722987
    7. results thus suggest that HERC2 regulates the basal turnover of FBXL5, and that this ubiquitin-dependent degradation pathway contributes to the control of mammalian iron metabolism PMID: 24778179
    8. identified HERC2, a HECT domain-containing E3 ligase, as being responsible for polyubiquitination of USP33. PMID: 24855649
    9. given a particular HERC2/OCA2 genotype, males are more prone to have lighter eye colors than predicted by their genotypes, while females tend to have darker eye colors than predicted PMID: 23601698
    10. Studied an autosomal-recessive neurodevelopmental disorder with some phenotypic similarities to Angelman syndrome, found among the Old Order Amish. Our molecular investigation identified a mutation in HERC2 associated with the disease phenotype. PMID: 23243086
    11. Pathogenic changes in HERC2 are associated with nonsyndromic intellectual disability, autism, and gait disturbance. PMID: 23065719
    12. the NEURL4-HERC2 complex participates in the ubiquitin-dependent regulation of centrosome architecture PMID: 22261722
    13. HERC2 rs12913832 region functions as an enhancer regulating OCA2 transcription. PMID: 22234890
    14. In response to double-strand breaks, both HERC2 and RNF168 were specifically modified with SUMO1 at double-strand break sites in a manner dependent on the SUMO E3 ligase PIAS4. PMID: 22508508
    15. These results suggest that HERC2 regulates DNA replication progression and origin firing by facilitating MCM2 phosphorylation. PMID: 21775519
    16. ). Sequence variations in rs11636232 and rs7170852 in HERC2, rs1800407 in OCA2 and rs16891982 in MATP showed additional association with eye colours PMID: 20457063
    17. role in pigmentation characteristics in Spanish population PMID: 20629734
    18. Findings identify a function for HERC2 in regulating BRCA1 stability in opposition to BARD1. The HERC2 expression in breast epithelial cells and breast carcinomas suggests that this mechanism may play a role in breast carcinogenesis. PMID: 20631078
    19. Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression PMID: 18172690
    20. We suggest that genetic variants regulating expression of the OCA2 gene exist in the HERC2 gene or, alternatively, within the 11.7 kb of sequence between OCA2 and HERC2, and that most iris color variation in Europeans is explained by those two genes. PMID: 18252221
    21. A single SNP in an evolutionary conserved region within intron 86 of the HERC2 gene determines human blue-brown eye color. PMID: 18252222
    22. Single nucleotide polymorphism in HERC2 gene is associated with ulcerative colitis PMID: 18438405
    23. OCA2 and HERC2 have roles in hair color in Australian adolescents PMID: 18528436
    24. Results confirmed the association of HERC2 rs12913832 with eye colour and showed that this SNP is also significantly associated with skin and hair colouration. PMID: 19208107
    25. Two single nucleotide polymorphisms found in intron 86 (rs12913832) and the 3' UTR region (rs1129038) of the HERC2 gene. PMID: 19472299

    顯示更多

    收起更多

  • 相關疾?。?/div>
    Mental retardation, autosomal recessive 38 (MRT38)
  • 亞細胞定位：
    Cytoplasm. Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriole. Nucleus. Note=Recruited to sites of DNA damage in response to ionizing radiation (IR) via its interaction with RNF8. May loose association with centrosomes during mitosis.
  • 數據庫鏈接：

    HGNC: 4868

    OMIM: 227220

    KEGG: hsa:8924

    STRING: 9606.ENSP00000261609

    UniGene: Hs.434890



主站蜘蛛池模板： 精品偷自拍另类在线观看| 亚洲爆乳精品无码一区二区| 娇妻玩4p被三个男人伺候电影 | 欧美人与动牲交a欧美| 色欲色香天天天综合网站| 99精品免视看| 国产成人一区二区三区在线| 国自产拍偷拍精品啪啪模特 | 99久久国产综合精品1| 国产精品无码一区二区三区在 | 亚欧av无码乱码在线观看性色| 久久精品一区二区三区中文字幕| 亚洲国产精品久久久久久| 久久久久久无码日韩欧美| 欧洲美女熟乱av| 亚洲色婷婷一区二区三区| 伊人成年网站综合网| 精品国产亚洲午夜精品av | 少妇大胆瓣开下部自慰| 国产呻吟久久久久久久92 | 偷偷要色偷偷中文无码| 乌克兰美女浓毛bbw| 国产欧美va欧美va香蕉在线| 国产老熟女网站| 久草热8精品视频在线观看| 综合色就爱涩涩涩综合婷婷| 一本色道久久综合亚洲精品 | 国内丰满熟女出轨videos| 成熟妇人a片免费看网站| 人人妻人人做人人爽| 中文字幕中文有码在线| 小13箩利洗澡无码视频网站| 欧美高清在线精品一区| 白丝乳交内射一二三区| 18禁男女无遮挡啪啪网站| 亚洲精品一区久久久久一品av| 亚洲乱亚洲乱妇24p| 少妇午夜福利一区二区 | 97色偷偷色噜噜狠狠爱网站 | 亚洲精品一区二区三区蜜臀| 青青草国产免费久久久|