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 Probable E3 ubiquitin-protein ligase makorin-3 (MKRN3)

Recombinant Human Probable E3 ubiquitin-protein ligase makorin-3 (MKRN3)

  • 中文名稱：
    人MKRN3重組蛋白
  • 貨號：
    CSB-EP618755HU
  • 規格：
    ￥1536
  • 圖片：
    • (Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.
  • 其他：

產品詳情

  • 純度：
    Greater than 90% as determined by SDS-PAGE.
  • 基因名：
    MKRN3
  • Uniprot No.：
  • 別名：
    D15S9; Makorin ring finger protein 3; Mkrn3; MKRN3_HUMAN; Probable E3 ubiquitin-protein ligase makorin-3; RING finger protein 63; RNF63; ZFP127; Zinc finger protein 127; ZNF127
  • 種屬：
    Homo sapiens (Human)
  • 蛋白長度：
    Full Length
  • 來源：
    E.coli
  • 分子量：
    60.6kDa
  • 表達區域：
    1-507aa
  • 氨基酸序列
    MEEPAAPSEAHEAAGAQAGAEAAREGVSGPDLPVCEPSGESAAPDSALPHAARGWAPFPVAPVPAHLRRGGLRPAPASGGGAWPSPLPSRSSGIWTKQIICRYYIHGQCKEGENCRYSHDLSGRKMATEGGVSPPGASAGGGPSTAAHIEPPTQEVAEAPPAASSLSLPVIGSAAERGFFEAERDNADRGAAGGAGVESWADAIEFVPGQPYRGRWVASAPEAPLQSSETERKQMAVGSGLRFCYYASRGVCFRGESCMYLHGDICDMCGLQTLHPMDAAQREEHMRACIEAHEKDMELSFAVQRGMDKVCGICMEVVYEKANPNDRRFGILSNCNHSFCIRCIRRWRSARQFENRIVKSCPQCRVTSELVIPSEFWVEEEEEKQKLIQQYKEAMSNKACRYFAEGRGNCPFGDTCFYKHEYPEGWGDEPPGPGGGSFSAYWHQLVEPVRMGEGNMLYKSIKKELVVLRLASLLFKRFLSLRDELPFSEDQWDLLHYELEEYFNLIL
    Note: The complete sequence may include tag sequence, target protein sequence, linker sequence and extra sequence that is translated with the protein sequence for the purpose(s) of secretion, stability, solubility, etc.
    If the exact amino acid sequence of this recombinant protein is critical to your application, please explicitly request the full and complete sequence of this protein before ordering.
  • 蛋白標簽：
    N-terminal 10xHis-tagged and C-terminal Myc-tagged
  • 產品提供形式：
    Liquid or 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.
  • 緩沖液：
    If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol.
    Note: If you have any special requirement for the glycerol content, please remark when you place the order.
    If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose.
  • 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：
    Basically, we can dispatch the products out in 1-3 working days after receiving your orders. 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 & COA：
    Please contact us to get it.

產品評價

靶點詳情

  • 功能：
    E3 ubiquitin ligase catalyzing the covalent attachment of ubiquitin moieties onto substrate proteins.
  • 基因功能參考文獻：
    1. MKRN3 is involvedt in central precocious puberty also in absence of deleterious mutations, although our sample size is small. Role of MKRN3 in the complex mechanism controlling puberty onset and its interaction with other factors affecting puberty such as nutrition. PMID: 28299573
    2. MKRN3 23566445 C/T polymorphism was associated with precocious puberty. PMID: 28988223
    3. The prevalence of MKRN3 mutations in our cohort of girls with central precocious puberty was similar to that reported in the literature in sporadic cases but lower than previously described in familial ones. PMID: 28672280
    4. Data suggest that a familial case of CPP (central precocious puberty) in which three out of four girls are affected is due to a novel MKRN3 nonsense mutation (p.Glu298Ter, N/E298); the affected siblings are the proband/oldest sister and the youngest sisters, monozygotic twins; there are no sons in this family; the next-to-oldest sister and the father are carriers of this nonsense mutation. [CASE REPORT; LETTER] PMID: 28132164
    5. Two heterozygous frameshift mutations (c.441_441delG, p.H148Tfs*23 and c803_803delAT, p.M268Vfs*23) were described in the MKRN3 gene in 2 probands with familial idiopathic central precocious puberty and in some of their family members. These frameshift mutations create a premature stop codon and result in a truncated protein. PMID: 27798941
    6. This study demonstrated a high frequency of MKRN3 mutations in boys with Central Precocious Puberty , previously classified as idiopathic, suggesting the importance of genetic analysis in this group. PMID: 27225315
    7. The genetic findings in our patients' cohort with central precocious puberty are in agreement with the hypothesis that the MKRN3 gene may act as an inhibitor of GnRH secretion during childhood. 13 It seems that MKRN3 gene alterations do not necessarily lead to early pubertal development in males, but paternally inherited MKRN3 mutations are responsible for central precocious puberty in females. PMID: 27640350
    8. MKRN3 is the most frequent genetic cause of familial Idiopathic Central Precocious Puberty, so it is wise to screen for MKRN3 mutations in all patients with familial Idiopathic Central Precocious Puberty and in patients with an unclear paternal pubertal history. PMID: 27931036
    9. Declining MKRN3 before pubertal onset support MKRN3 as an inhibitor of GnRH secretion during midchildhood. PMID: 27057785
    10. The identification of carriers of MKRN3 mutations may contribute to early diagnosis of Central Precocious Puberty, facilitating treatment decisions and guiding genetic counseling and prompt intervention in familial cases. PMID: 27424312
    11. Peripheral MKRN3 levels in boys appear to serve as a readout of the diminishing central inhibition that controls the onset of puberty. PMID: 27025240
    12. Data show similar circulating MKRN3 levels in men with congenital hypogonadotropic hypogonadism (CHH)and healthy controls. PMID: 26175221
    13. Data indicate that a novel mutation in the makorin ring finger protein 3 (MKRN3) gene in two sisters with central precocious puberty (CPP) was identified. PMID: 26173472
    14. the present study reveals a relatively low number of MKRN 3 mutations in Korean girls with CPP. PMID: 25938887
    15. Case Report: MKRN3 missense mutation in a Danish girl with central precocious puberty and her brother with early puberty. PMID: 26331766
    16. prevalence of MKNR3 mutations is high in familial cases of idiopathic central precocious puberty (iCPP); onset occurs earlier in patients with MKRN3 mutations than in those without the mutations and sexual dimorphism for age at puberty onset persists in patients with mutations; MKRN3 mutations accelerate postnatal development of the gonadotropic axis PMID: 26431553
    17. MKRN3 plays an inhibitory role in the reproductive axis to represent a new pathway in pubertal regulation. [Review] PMID: 25957321
    18. Declining levels of circulating MKRN3 preceded pubertal onset. The negative correlation between MKRN3 and gonadotropins further supports MKRN3 as a major regulator of hypothalamic GnRH secretion during childhood. PMID: 25695892
    19. The MKRN3 protein has a fundamental role in determining pubertal timing. PMID: 25316453
    20. MKRN3 mutations appear to be a frequent cause of familial CPP and, considering the imprinted mode of inheritance, may also account for a certain proportion of isolated CPP cases. PMID: 25011910
    21. this study identified novel inherited MKRN3 defects in children with apparently sporadic central precocious puberty, supporting a fundamental role of this peptide in the suppression of the reproductive axis. PMID: 24628548
    22. A novel MKRN3 mutation (p.C340G) in a girl with central precocious puberty and her brother with early puberty. PMID: 24438377
    23. Deficiency of MKRN3 causes central precocious puberty in humans. PMID: 23738509
    24. MKRN3 gene is imprinted, with preferential expression from the paternal allele. PMID: 10196367

    顯示更多

    收起更多

  • 相關疾病：
    Precocious puberty, central 2 (CPPB2)
  • 組織特異性：
    Ubiquitous.
  • 數據庫鏈接：

    HGNC: 7114

    OMIM: 603856

    KEGG: hsa:7681

    STRING: 9606.ENSP00000313881

    UniGene: Hs.679587



主站蜘蛛池模板： 亚洲码欧美码一区二区三区 | 97无码免费人妻超级碰碰碰碰 | 麻豆国产成人av在线播放欲色| 天天综合爱天天综合色| 激情按摩系列片aaaa| 亚洲 成人 无码 在线观看| 久久视频在线视频| 日本亚洲vr欧美不卡高清专区| 亚洲天天做日日做天天欢毛片| 搡女人真爽免费视频大全| 人人妻人人藻人人爽欧美一区| 国产午夜片无码区在线观看爱情网| 青青草国产免费国产是公开| 免费网站观看www在线观看| 久久久久成人精品免费播放动漫| 国产综合色在线视频区| 在线看片免费人成视频在线影院 | 免费视频成人片在线观看| 一区二区三区在线 | 日本| 久久精品蜜芽亚洲国产av| 国语国产精精品国产国语清晰对话 | 国产手机在线国内精品| 理论片午午伦夜理片影院| 青楼妓女禁脔道具调教sm| 亚洲毛片αv无线播放一区 | av不卡国产在线观看| 色yeye香蕉凹凸视频在线观看| 精品国产av 无码一区二区三区 | 亚洲中文字幕aⅴ无码天堂| 少妇爱做高清免费视频| 欧美人与物videos另类| 日本强伦姧人妻一区二区| 国产偷久久久精品专区| 97色精品视频在线观看| 无套内谢老熟女| 天天拍夜夜添久久精品| 欧美人与动牲交免费观看网| 成人片黄网站色大片免费毛片| 色与欲影视天天看综合网| 五月综合缴情婷婷六月| 久久99精品国产麻豆婷婷洗澡|