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Recombinant Mouse Perforin-1 (Prf1)

In Stock
  • 中文名稱:
    小鼠Prf1重組蛋白
  • 貨號(hào):
    CSB-EP018668MO
  • 規(guī)格:
    ¥2328
  • 圖片:
    • (Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.
  • 其他:

產(chǎn)品詳情

  • 純度:
    Greater than 85% as determined by SDS-PAGE.
  • 基因名:
  • Uniprot No.:
  • 別名:
    Prf1; Pfp; Perforin-1; P1; Cytolysin; Lymphocyte pore-forming protein
  • 種屬:
    Mus musculus (Mouse)
  • 蛋白長度:
    Full Length of Mature Protein
  • 來源:
    E.coli
  • 分子量:
    63.9 kDa
  • 表達(dá)區(qū)域:
    21-554aa
  • 氨基酸序列
    PCYTATRSECKQKHKFVPGVWMAGEGMDVTTLRRSGSFPVNTQRFLRPDRTCTLCKNSLMRDATQRLPVAITHWRPHSSHCQRNVAAAKVHSTEGVAREAAANINNDWRVGLDVNPRPEANMRASVAGSHSKVANFAAEKTYQDQYNFNSDTVECRMYSFRLVQKPPLHLDFKKALRALPRNFNSSTEHAYHRLISSYGTHFITAVDLGGRISVLTALRTCQLTLNGLTADEVGDCLNVEAQVSIGAQASVSSEYKACEEKKKQHKMATSFHQTYRERHVEVLGGPLDSTHDLLFGNQATPEQFSTWTASLPSNPGLVDYSLEPLHTLLEEQNPKREALRQAISHYIMSRARWQNCSRPCRSGQHKSSHDSCQCECQDSKVTNQDCCPRQRGLAHLVVSNFRAEHLWGDYTTATDAYLKVFFGGQEFRTGVVWNNNNPRWTDKMDFENVLLSTGGPLRVQVWDADYGWDDDLLGSCDRSPHSGFHEVTCELNHGRVKFSYHAKCLPHLTGGTCLEYAPQGLLGDPPGNRSGAVW
    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(biāo)簽:
    N-terminal 6xHis-tagged
  • 產(chǎn)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:
    Tris-based buffer,50% glycerol
  • 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:
    3-7 business days
  • 注意事項(xiàng):
    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(chǎn)品評價(jià)

靶點(diǎn)詳情

  • 功能:
    Plays a key role in secretory granule-dependent cell death, and in defense against virus-infected or neoplastic cells. Can insert into the membrane of target cells in its calcium-bound form, oligomerize and form large pores. Promotes cytolysis and apoptosis of target cells by facilitating the uptake of cytotoxic granzymes.
  • 基因功能參考文獻(xiàn):
    1. Study in mice models shows that perforin from antigen-specific cytotoxic T lymphocytes is required for Nlrp3 inflammasome activation in antigen-presenting cells. Furthermore, such activation of NLRP3 inflammasome contributes to the induction of antigen-specific antitumour immunity and pathogenesis of graft-versus-host diseases. PMID: 28537251
    2. levetiracetam can still protect neurons with perforin knockout mice. PMID: 26454821
    3. These studies indicate that CD8+ T cells against a single antigen can restrict Y. pseudotuberculosis colonization in a perforin-dependent manner, but ultimately are insufficient in their ability to provide sterilizing immunity and protect against death. PMID: 27268148
    4. Furthermore, perforin production specifically by CD8 T cells was required to cause fatal edema during experimental cerebral malaria. PMID: 28264905
    5. Our study suggests that perforin plays a role in dopaminergic neuron loss in PD. PMID: 28137589
    6. study shows that perforin is essential to facilitate beta cell destruction in mouse models of type 1 diabetes PMID: 26446877
    7. Released granzyme B induces DNA fragmentation in intraepithelial lymphocytes independently of Perforin PMID: 25750028
    8. serglycin plays a critical role in the maturation of dense-core cytotoxic granules in cytotoxic lymphocytes and the trafficking and storage of perforin and granzyme B, whereas granzyme A is unaffected PMID: 26756195
    9. This suggests that LPS alters UNK cell migration and activates cytotoxic granule release. PMID: 26066976
    10. it is proposed that Ca(2+) binding at the weakest affinity site triggers changes in the perforin C2 domain that facilitate its interaction with lipid membranes PMID: 26306037
    11. a lack of perforin and absence of the specific activation of NK cells during acute MCMV infection lead to an unleashed CD8(+) T cell response that is detrimental for the host. PMID: 25809566
    12. CD8 T cells are sufficient as a sole perforin-expressing cell type to cause BBB disruption in the PIFS model. PMID: 25337791
    13. The rate and proportion of donor lymphoid cell engraftment and expansion of effector memory donor T cells were significantly increased within 5 to 7 days post-bone marrow transplantation in perforin-deficient recipients, compared with wild-type. PMID: 25459639
    14. Regulatory effects of perforin on glucose tolerance are mechanistically linked to the control of T-cell proliferation and cytokine production in inflamed visceral adipose tissue. PMID: 25048196
    15. Perforin (and granzyme B)-dependent apoptosis increases postapoptotic necrosis and inflammation in atherosclerosis. PMID: 25398236
    16. Perforin has a role in atherosclerotic plaque development. PMID: 24205352
    17. Defining the interaction of perforin with calcium and the phospholipid membrane. PMID: 24070258
    18. miR-150 is a common post-transcriptional regulator for Prf1 in mouse and human NK cells that represses NK cell lytic activity. PMID: 24698324
    19. Perforin and granzymes have complementary roles mediating epithelial injury by NK and CD8 T cells. The prevention of experimental biliary atresia can only be achieved by inhibiting both granules. PMID: 24096050
    20. Multiple roles of perforin in hampering ERBB-2 (Her-2/neu) carcinogenesis in transgenic male mice. PMID: 24790144
    21. perforin preferentially delivers cationic molecules while anionic and neutral cargoes are delivered inefficiently PMID: 24558045
    22. perforin's contribution to bacterial clearance in vivo is not though enhancing CD4 T cell termination of Chlamydia replication in epithelial cells PMID: 23691028
    23. These findings demonstrate that perforin-mediated immunoregulation functions in trans and are consistent with a feedback model in which cytotoxic T cells control immune activation by killing dendritic cells. PMID: 23974195
    24. These data suggest that perforin expression is not required for normal immune regulation. PMID: 23883515
    25. Distinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11. PMID: 23160464
    26. Perforin facilitates viral antigen uptake by pulmonary dendritic cells by inducing apoptosis in mice with influenza infection. PMID: 22869906
    27. Perforin/FasL-independent functions of hapten-primed CD8 T cells in a contact hypersensitivity model identify new functions for neutrophils in regulating effector CD8 T cell recruitment and immune responses in the skin. PMID: 22815291
    28. deficiency of T-cells, NKT-cells, perforin, Fas-ligand, TNF-alpha-receptor failed to reveal significant differences in tumor development. PMID: 22212899
    29. CD8+ T-cells expressing interferon gamma or perforin play antagonistic roles in heart injury in experimental Trypanosoma cruzi-elicited cardiomyopathy PMID: 22532799
    30. CD4 cells expressing gamma interferon and perforin mediate protection against lethal influenza virus infection. PMID: 22491469
    31. A perforin-dependent pathwy plays a role to mediate contraction of antigen-specific CD8+ and CD4+ T cells during prolonged Listeria monocytogenes infection. PMID: 22161269
    32. Data show that transitional stage 1, 2 and splenic marginal zone B cells were clearly reduced after transfer of CD4+ T cells from TNFalpha-/-, IFNgamma-/-, perforin-/-, or FasLgld mice. PMID: 21966366
    33. Structures that PFN oligomers form in the membrane bilayer may include arcs previously observed by electron microscopy and these unusual structures represent an incomplete mixture of plasma membrane lipid. PMID: 21931672
    34. We conclude that perforin-dependent cytotoxicity has an immunoregulatory role that is distinguishable from its pathogen clearance function and limits T-cell activation in the physiologic context by suppressing antigen presentation. PMID: 21606480
    35. intact C terminus and N-linked glycosylation provide accurate and efficient export of perforin from the endoplasmic reticulum to the secretory granules and are critical for cytotoxic lymphocyte survival PMID: 21658975
    36. Data suggest that an interdependent relationship between parasite burden and CD8(+) T cells dictates the onset of perforin/GzmB-mediated ECM. PMID: 21525386
    37. Transcription and translation products of the cytolysin gene psm-mec on the mobile genetic element SCCmec regulate Staphylococcus aureus virulence. PMID: 21304931
    38. At the Prf1 locus, clear areas of reduced nucleosomal density are detected in effector CD8-positive T cells surrounding the transcription start site but not in downstream areas of the genes, during lymphocytic choriomeningitis viral infection. PMID: 21278341
    39. Perforin was dispensable for efficient clearance of antigen-bearing cells from immunized mice, but only if CD95/CD95L was functional; however, there was a delay in target cell clearance in the absence of perforin. PMID: 20309009
    40. Granule-bound cathepsins are essential for processing perforin to its active form, and that CatL is an important, but not exclusive, participant in this process. PMID: 20497254
    41. elucidation of the mechanism of perforin pore formation by determining the X-ray crystal structure of monomeric murine perforin, together with a cryo-electron microscopy reconstruction of the entire perforin pore PMID: 21037563
    42. Perforin-mediated cytotoxicity by CD8 T cells is definitively responsible for muscle injury in C protein-induced myositis (CIM) PMID: 20583106
    43. Perforin deficiency attenuates inflammation and tumor growth in colitis-associated cancer. PMID: 19785028
    44. Pathogenetically relevant immune reactions in proteolipid protein-overexpressing mice are TCR-dependent and mediated by the classical components of CD8+ T-cell cytotoxicity, perforin, and Gzmb. PMID: 20042681
    45. role for perforin-, Fas/FasL-, and TNFR1-mediated cytotoxic pathways in down-regulation of antigen-specific T cells during persistent viral infection PMID: 11752172
    46. Using perforin-knockout (PKO) mice, we have seen that the granule exocytosis pathway can play a major role in NK cell-mediated rejection of allogeneic and MHC class I-deficient BMC, depending upon the genetics of the recipient and housing conditions. PMID: 11870623
    47. An intronic silencer of the mouse perforin gene. PMID: 11911476
    48. the genes for perforin, the three major T cell granzymes (A-C) and IFN-gamma are differentially expressed during primary activation of naive CD8(+) T cells, kinetically and at the single-cell level PMID: 12039912
    49. The immunodominance hierarchy of influenza virus-specific T(CD8+) was not greatly perturbed by the absence of either perforin or T-helper cells or by interference with B7 (CD80)-mediated signaling. PMID: 12239309
    50. Perforin protein expression is severely impaired in MEF-deficient NK cells PMID: 12387738

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  • 亞細(xì)胞定位:
    Cytolytic granule. Secreted. Cell membrane; Multi-pass membrane protein. Endosome lumen.
  • 蛋白家族:
    Complement C6/C7/C8/C9 family
  • 組織特異性:
    Detected in cytotoxic T-lymphocytes and natural killer cells.
  • 數(shù)據(jù)庫鏈接:


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