RIP3(RIPK3,Receptor Interacting Protein 3),受體相互作用蛋白3,是一種重要的蛋白質,在細胞凋亡過程中起著關鍵作用。近年來,RIP3蛋白研究取得了顯著進展。首先,研究人員發現RIP3蛋白與許多其他重要的蛋白質相互作用,從而參與了細胞凋亡的誘導和調節。其中,一些研究表明RIP3蛋白與蛋白質復合物Necrosome相關,這是一個重要的細胞凋亡誘導機制。此外,RIP3蛋白也與細胞凋亡調節因子、蛋白酶以及其他蛋白質相互作用,參與了細胞凋亡的誘導和調節。隨著新病毒如SARS-CoV-2的出現以及流感、MPOX和RSV等已知病毒的激增,RIPK 3已成為研究和治療的首要靶點,但最近的研究表明,它是幾種炎癥性疾病、退行性疾病甚至癌癥的可行靶點。
艾美捷科技為您推薦ProSci,經敲除驗證的RIP3 / RIPK3抗體(貨號PSI-2283),已被廣泛引用,在抗體引文跟蹤器CiteAb上被引用多達171次,在Bioz上被引用多達165次。我們抗體的可靠性促成了它的受歡迎程度,在許多頂級期刊上發表的研究中,包括《Nature》《Cell》《Nature Medicine》。至關重要的是,我們的抗體已經參與了很多與治療學開發相關的研究,以及冠狀病毒和COVID-19療法有關的研究。
抗體名稱 | RIP3 抗體 |
貨號 | PSI-2283 |
克隆性 | 多克隆 |
應用類型 | E, IF, IHC-P, IP, WB |
宿主來源 | 兔 |
反應種屬 | 人類、小鼠、大鼠 |
以下幾篇文章展示了在您的研究中使用ProSci抗體的療效:
- Karki R, Lee S, Mall R, et al. ZBP1-dependent inflammatory cell death, PANoptosis, and cytokine storm disrupt IFN therapeutic efficacy during coronavirus infection. Sci Immunol. 2022;7(74):eabo6294. doi:10.1126/sciimmunol.abo6294
- Lee S, Karki R, Wang Y, Nguyen LN, Kalathur RC, Kanneganti TD. AIM2 forms a complex with pyrin and ZBP1 to drive PANoptosis and host defence. Nature. 2021;597(7876):415-419. doi:10.1038/s41586-021-03875-8
- Zhang T, Yin C, Boyd DF, et al. Influenza Virus Z-RNAs Induce ZBP1-Mediated Necroptosis. Cell. 2020;180(6):1115-1129.e13. doi:10.1016/j.cell.2020.02.050
- Zheng M, Karki R, Vogel P, Kanneganti TD. Caspase-6 Is a Key Regulator of Innate Immunity, Inflammasome Activation, and Host Defense. Cell. 2020;181(3):674-687.e13. doi:10.1016/j.cell.2020.03.040
RIP3 / RIPK3抗體相關產品推薦:
- RIPK1 ,貨號:PSI--5389(50篇以上文章)
- MLKL ,貨號:PSI--14-026
- TRIF ,貨號:PSI--3173(50篇以上文章)
- FADD ,貨號:PSI--18-232, 18-273 (KO Validated)
- cFLIP ,貨號:PSI--1159(50篇以上文章)
- NLRP3 ,貨號:PSI--5447(50篇以上文章)
- NOD2 ,貨號:PSI--2513(50篇以上文章)
- Caspase8 ,貨號:PSI--3473(50篇以上文章)
RIP3 / RIPK3抗體更多發表文章:
- He et al. Receptor interacting protein kinase-3 determines cellular necrotic response to TNF-alpha. Cell. 2009;137(6):1100-11. PMID: 19524512
- Zhang et al. Functional complementation between FADD and RIP1 in embryos and lymphocytes. Nature. 2011;471(7338):373-6. PMID: 21368761
- Narayan et al. The NAD-dependent deacetylase SIRT2 is required for programmed necrosis. Nature. 2012;492(7428):199-204. PMID: ??23201684
- Li et al. Tissue damage negatively regulates LPS-induced macrophage necroptosis. Cell Death Differ. 2016;23(9):1428-47. doi:10.1038/cdd.2016.21. Epub 2016. PMID: ???????26943325
- Yang et al. Regulation of RIP3 by the transcription factor Sp1 and the epigenetic regulator UHRF1 modulates cancer cell necroptosis. Cell Death Dis. 2017;8(10):e3084. doi:10.1038/cddis.2017.483. PMID: 28981102
- Ramachandran et al. Receptor interacting protein kinase 3 is a critical early mediator of acetaminophen-induced hepatocyte necrosis in mice. Hepatology. 2013;58(6):2099-108. PMID: 23744808
- Li et al. The RIP1/RIP3 necrosome forms a functional amyloid signaling complex required for programmed necrosis. Cell. 2012 ;150(2):339-50. PMID: ???????22817896
- Vitner et al. RIPK3 as a potential therapeutic target for Gaucher's disease. Nat Med. 2014;20(2):204-8. PMID: 24441827
- Wang et al. RNA viruses promote activation of the NLRP3 inflammasome through a RIP1-RIP3-DRP1 signaling pathway. Nat Immunol. 2014;15(12):1126-33. PMID: 25326752
- Onizawa et al. The ubiquitin-modifying enzyme A20 restricts ubiquitination of the kinase RIPK3 and protects cells from necroptosis. Nat Immunol. 2015;16(6):618-27. PMID: 25939025
- Murphy et al. The pseudokinase MLKL mediates necroptosis via a molecular switch mechanism. Immunity. 2013;39(3):443-53. PMID: 24012422
- Nogusa et al. RIPK3 Activates Parallel Pathways of MLKL-Driven Necroptosis and FADD-Mediated Apoptosis to Protect against Influenza A Virus. Cell Host Microbe 2016;20(1):13-24. PMID: 27321907
- Pearson et al. EspL is a bacterial cysteine protease effector that cleaves RHIM proteins to block necroptosis and inflammation. Nat Microbiol. 2017 ;2:16258. PMID: 28085133
- Yang et al. The end of RIPK1-RIPK3-MLKL-mediated necroptosis in acetaminophen-induced hepatotoxicity? Hepatology. 2016;64(1):311-2PMID: 26418225
- Qu et al. Graphene oxide induces toll-like receptor 4 (TLR4)-dependent necrosisin macrophages. ACS Nano. 2013;7(7):5732-45.PMID: 23734789
- Gandhirajan et al. Blockade of NOX2 and STIM1 signaling limits Lipo polysaccharide-induced vascular inflammation. J Clin Invest. 2013;123(2):887-902. PMID: 23348743
- Fortes et al. Heme induces programmed necrosis on macrophages through autocrine TNF and ROS production. Blood. 2012;119(10):2368-75. PMID: 22262768
- Xu et al. The cytoplasmic nuclear receptor RARγ controls RIP1 initiated cell death when cIAP activity is inhibited. Nat Commun. 2017;8(1):425. PMID: 28871172
- Karunakaran et al. Targeting macrophage necroptosis for therapeutic and diagnostic interventions in atherosclerosis. Sci Adv. 2016 ;2(7):e1600224. PMID: 27532042
- Chen et al. Mechanisms of necroptosis in T cells. J Exp Med. 2011 Apr 11;208(4):633-41.PMID: 21402742
ProSci Incorporated于1998年成立于美國加州圣地亞哥市,從事抗體等科研試劑的研發、生產和銷售。產品涵蓋了細胞凋亡、信號轉導、免疫、腫瘤、細胞生物、神經生物、傳染病等領域。ProSci擁有超過30000種單克隆抗體和多克隆抗體。ProSci的抗體大都經免疫親和層析純化,具有高純度、高親和力、特異性強等特點,所有的ProSci抗體都經過了嚴格的驗證測試和質量控制,已保證高質量的產品。此外,ProSci還提供標記二抗,重組蛋白,細胞和組織裂解液,細胞涂片,組織切片,多肽等產品與抗體配套使用。