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 Histone deacetylase 5 (HDAC5), partial

  • 中文名稱:
    人HDAC5重組蛋白
  • 貨號:
    CSB-YP010241HU
  • 規(guī)格:
  • 來源:
    Yeast
  • 其他:
  • 中文名稱:
    人HDAC5重組蛋白
  • 貨號:
    CSB-EP010241HU
  • 規(guī)格:
  • 來源:
    E.coli
  • 其他:
  • 中文名稱:
    人HDAC5重組蛋白
  • 貨號:
    CSB-EP010241HU-B
  • 規(guī)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HDAC5重組蛋白
  • 貨號:
    CSB-BP010241HU
  • 規(guī)格:
  • 來源:
    Baculovirus
  • 其他:
  • 中文名稱:
    人HDAC5重組蛋白
  • 貨號:
    CSB-MP010241HU
  • 規(guī)格:
  • 來源:
    Mammalian cell
  • 其他:

產(chǎn)品詳情

  • 純度:
    >85% (SDS-PAGE)
  • 基因名:
  • Uniprot No.:
  • 別名:
    Antigen NY CO 9; Antigen NY-CO-9; HD5; HDAC 5; HDAC5; HDAC5_HUMAN; Histone deacetylase 5; NY CO 9
  • 種屬:
    Homo sapiens (Human)
  • 蛋白長度:
    Partial
  • 蛋白標(biāo)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(chǎn)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(fù)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(chǔ)存條件:
    Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.
  • 保質(zhì)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(xiàng):
    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(chǎn)品評價(jià)

靶點(diǎn)詳情

  • 功能:
    Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4). Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes. Involved in muscle maturation by repressing transcription of myocyte enhancer MEF2C. During muscle differentiation, it shuttles into the cytoplasm, allowing the expression of myocyte enhancer factors. Involved in the MTA1-mediated epigenetic regulation of ESR1 expression in breast cancer. Serves as a corepressor of RARA and causes its deacetylation. In association with RARA, plays a role in the repression of microRNA-10a and thereby in the inflammatory response.
  • 基因功能參考文獻(xiàn):
    1. These results demonstrate a previously unknown negative epigenetic regulation of hematopoietic stem cells (HSC) homing and engraftment by HDAC5, and allow for a new and simple translational strategy to enhance HSC transplantation. PMID: 30013077
    2. Collectively, these data indicate that vIRF3 alters global gene expression and induces a hypersprouting formation in an HDAC5-binding-dependent and lymphatic endothelial cell-specific manner, ultimately contributing to Kaposi's sarcoma-associated herpesvirus-associated pathogenesis. PMID: 29339432
    3. High HDAC5 expression is associated with invasion of lung cancer. PMID: 30066893
    4. HO-1 plays a key role in protecting tumor cells from apoptosis, in a process that involves Smad7 and HDAC4/5 in apoptosis of B-ALL cells PMID: 29886060
    5. These findings demonstrate a novel mechanism for deregulation of HDAC5 in non-small cell lung cancer (NSCLC)and suggest that miR5895p/HDAC5 pathway may represent a new prognostic biomarker and therapeutic target against NSCLC. PMID: 28440397
    6. HDAC5 was extensively expressed in human BC tissues, and high HDAC5 expression was associated with an inferior prognosis. PMID: 27177225
    7. HDAC5 is a negative predictor of disease-free and overall survival in pancreatic neuroendocrine tumor patients. PMID: 28235630
    8. Interference with both glucose and glutamine supply in HDAC5-inhibited cancer cells significantly increases apoptotic cell death. PMID: 28414307
    9. these results suggest that HDAC5 is critical in regulating LSD1 protein stability through post-translational modification, and the HDAC5-LSD1 axis has an important role in promoting breast cancer development and progression. PMID: 27212032
    10. The expression of HDAC5 was significantly increased in endothelial cells (ECs) from patients with systemic sclerosis (SSc) compared to healthy control endothelial cells. Silencing of HDAC5 in SSc ECs restored normal angiogenesis. HDAC5 knockdown followed by ATAC-seq assay in SSc ECs identified key HDAC5-regulated genes involved in angiogenesis and fibrosis, such as CYR61, PVRL2, and FSTL1. PMID: 27482699
    11. the migration and invasion of hepatocellular carcinoma cells were impaired by knockdown of histone deacetylase 5 or hypoxia-inducible factor-1alpha but rescued when eliminating homeodomain-interacting protein kinase-2 in hepatocellular carcinoma cells, which suggested the critical role of histone deacetylase 5-homeodomain-interacting protein kinase-2-hypoxia-inducible factor-1alpha pathway in hypoxia-induced metastasis. PMID: 28653891
    12. HDAC5 inhibits hepatic lipogenic genes expression by attenuating the transcriptional activity of liver X receptor. PMID: 27614433
    13. HDAC5 promotes cellular proliferation through the upregulation of cMet, and may provide a novel therapeutic target for the treatment of patients with Wilms' tumor. PMID: 26847592
    14. Formononetin-combined therapy may enhance the therapeutic efficacy of doxorubicin in glioma cells by preventing EMT through inhibition of HDAC5. PMID: 26261519
    15. These results suggest a strong regulatory function of HDAC5 in the pro-inflammatory response of macrophages. PMID: 26059794
    16. In erythroid cells, pull down experiments identified the presence of a novel complex formed by HDAC5, GATA1, EKLF and pERK which was instead undetectable in cells of the megakaryocytic lineage. PMID: 24594363
    17. Data reveal a novel role of HDAC5 in modulating the KLF2 transcriptional activation and eNOS expression. PMID: 25096223
    18. Studied phosphorylation sites within functional HDAC5 domains, including the deacetylation domain (DAC, Ser755), nuclear export signal (NES, Ser1108), and an acidic domain (AD, Ser611). PMID: 24920159
    19. mRNA and protein levels of HDAC5 were up-regulated in human hepatocellular carcinoma. PMID: 25129440
    20. HDAC5 promoted the Six1 expression. PMID: 24706304
    21. In C2C12 myoblasts, recombinant human HDAC5 phosphorylation by PKD regulated the expression of diverse metabolic genes and glucose metabolism. PMID: 24732133
    22. findings show N-Myc upregulated HDAC5 expression in neuroblastoma cells; HDAC5 repressed NEDD4 gene expression,increased Aurora A gene expression and consequently upregulated N-Myc protein expression;data identify HDAC5 as a novel co-factor in N-Myc oncogenesis PMID: 23812427
    23. we show that Stat3 binds to the promoter region of PTPN13 and promotes its activity through recruiting HDAC5. Thus, our results suggest a previously unknown Stat3-PTPN13 molecular network controlling squamous cell lung carcinoma development PMID: 24191246
    24. At the molecular level, we demonstrated that HDAC5 promoted mRNA expression of twist 1, which has been reported as an oncogene PMID: 24092570
    25. These findings suggest that HDAC5 is a key determinant of p53-mediated cell fate decisions in response to genotoxic stress. PMID: 24120667
    26. Data indicate there was a link between baseline viral load, age (40 years), IL-28B (rs12979860), HDAC2 (rs3778216), HDAC3 (rs976552) and HDAC5 (rs368328) with sustained virological response (SVR). PMID: 23615070
    27. HDAC5 is essential for the length maintenance of long telomeres and its depletion is required for sensitization of cancer cells with long telomeres to chemotherapy. PMID: 23729589
    28. Loss of HDAC5 impairs memory function but has little impact in a transgenic mouse model of amyloid pathology. PMID: 22914591
    29. Nuclear calcium signaling is a regulator of nuclear export of HDAC4 and HDAC5. PMID: 23364788
    30. Dephosphorylation at a conserved SP motif governs cAMP sensitivity and nuclear localization of class IIa histone deacetylases HDAC4, 5 and 9 PMID: 23297420
    31. Data suggest that HDAC5 regulates muscle glucose metabolism and insulin action and that HDAC inhibitors can be used to modulate these parameters in muscle cells. PMID: 22991226
    32. The current study identified the class II deacetylase HDAC5 as a novel promoting factor of CTG*CAG expansions. PMID: 22941650
    33. HDAC5 in the maintenance/assembly of pericentric heterochromatin structure and demonstrate that class IIa HDAC5 can represent a potential target for anticancer therapies. PMID: 22301920
    34. The results of this study suggested that suggest that HDAC5 provides a delayed braking mechanism on gene expression programs that support the development, but not expression, of cocaine reward behaviors. PMID: 22243750
    35. Significantly increased methylation of the HDAC5 gene was associated with astrocytomas. PMID: 21508384
    36. Ser279 is a critical phosphorylation within the NLS involved in the nuclear import of HDAC5 PMID: 21081666
    37. in addition to activation of protein kinase D isozymes by phosphorylating Ser744 and Ser748 at their activation sites, PKCdelta may also play a role in the regulation of HDAC5 by phosphorylation of Ser259 PMID: 21146494
    38. differentiation-dependent GLUT4 gene expression in 3T3-L1 adipocytes is dependent on the nuclear concentration of a class II histone deacetylase (HDAC) protein, HDAC5 PMID: 21047791
    39. Findings identify HDAC5 as a substrate of PKA and reveal a cAMP/PKA-dependent pathway that controls HDAC5 nucleocytoplasmic shuttling and represses gene transcription. PMID: 20716686
    40. phosphorylation-dependent derepression of HDAC5 mediates flow-induced KLF2 and eNOS expression as well as flow anti-inflammation, and suggest that HDAC5 could be a potential therapeutic target for the prevention of atherosclerosis. PMID: 20042720
    41. Class II histone deacetylases are directly recruited by BCL6 transcriptional repressor PMID: 11929873
    42. Histone deacetylase 5 is not a p53 target gene, but its overexpression inhibits tumor cell growth and induces apoptosis. PMID: 12019172
    43. MITR, HDAC4, and HDAC5 associate with heterochromatin protein 1 (HP1), an adaptor protein that recognizes methylated lysines within histone tails and mediates transcriptional repression by recruiting histone methyltransferase PMID: 12242305
    44. HDAC5 binds to Ca(2+)/calmodulin and inhibits MEF2a binding PMID: 12626519
    45. ICP0 of herpes simplex virus Type 1 is able to overcome the HDAC5 amino-terminal- and MITR-induced MEF2A repression in gene reporter assays PMID: 15194749
    46. The HDAC5, a class II HDAC involved in myogenesis, was not detected in the tissues. PMID: 15590418
    47. G betagamma binds HDAC5 and inhibits its transcriptional co-repression activity PMID: 16221676
    48. novel transcriptional pathway under the control of class II HDACs and suggest a role for these transcriptional repressors as signal-responsive regulators of antigen presentation PMID: 16236793
    49. NO-dependent PP2A activation plays a key role in nuclear translocation of class II HDACs HDAC4 and HDAC5 PMID: 17975112
    50. AMP-activated protein kinase (AMPK) regulates GLUT4 transcription through the histone deacetylase (HDAC)5 transcriptional repressor. PMID: 18184930

    顯示更多

    收起更多

  • 亞細(xì)胞定位:
    Nucleus. Cytoplasm. Note=Shuttles between the nucleus and the cytoplasm. In muscle cells, it shuttles into the cytoplasm during myocyte differentiation. The export to cytoplasm depends on the interaction with a 14-3-3 chaperone protein and is due to its phosphorylation at Ser-259 and Ser-498 by AMPK, CaMK1 and SIK1.
  • 蛋白家族:
    Histone deacetylase family, HD type 2 subfamily
  • 組織特異性:
    Ubiquitous.
  • 數(shù)據(jù)庫鏈接:

    HGNC: 14068

    OMIM: 605315

    KEGG: hsa:10014

    STRING: 9606.ENSP00000225983

    UniGene: Hs.438782



主站蜘蛛池模板: 欧美精品久久96人妻无码| 欧美亚洲国产精品久久蜜芽 | 国内揄拍高清国内精品对白| 国产伦精品一区二区三区妓女下载 | 狠狠躁天天躁无码中文字幕| 大伊香蕉精品一区视频在线 | 久久综合99re88久久爱| 日本一卡2卡三卡4卡免费网站| 免费国产线观看免费观看| 亚洲精品亚洲人成在线下载| 成人天堂婷婷青青视频在线观看| 亚洲日韩av无码一区二区三区人| 亚洲爆乳成av人在线蜜芽| 日日摸日日碰夜夜爽亚洲| 熟睡人妻被讨厌的公侵犯| 色多多www视频在线观看免费| 亚洲超碰无码色中文字幕97| 国产无遮挡又黄又爽免费视频| 熟妇女人妻丰满少妇中文字幕 | 无码乱肉视频免费大全合集| 色橹橹欧美在线观看视频高清| 精品久久久久久无码专区不卡| 天天爽夜夜爽人人爽从早干到睌| 男人的天堂免费一区二区视频| 毛片无遮挡高清免费| 色偷偷88888欧美精品久久久| 天堂俺去俺来也www色官网| 97色伦97色伦国产欧美| 少妇无码一区二区三区免费| 午夜无码片在线观看影院| 亚洲处破女av日韩精品波波网| 伊人色综合九久久天天蜜桃| av天堂午夜精品一区| 成人免费看吃奶视频网站 | av无码东京热亚洲男人的天堂| 精品熟女少妇av久久免费软件| 亚洲爱婷婷色婷婷五月| 亚无码乱人伦一区二区| 另类亚洲小说图片综合区| 暖暖视频日本| 两根大肉大捧一进一出好爽视频|