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Human Tumor necrosis factor alpha-induced protein 3(TNFAIP3) ELISA kit

  • 中文名稱:
    人腫瘤壞死因子α誘導(dǎo)蛋白3(TNFAIP3)酶聯(lián)免疫試劑盒
  • 貨號(hào):
    CSB-EL023958HU
  • 規(guī)格:
    96T/48T
  • 價(jià)格:
    ¥3600/¥2500
  • 其他:

產(chǎn)品詳情

  • 產(chǎn)品描述:
    人腫瘤壞死因子α誘導(dǎo)蛋白3(TNFAIP3)酶聯(lián)免疫試劑盒(CSB-EL023958HU)為雙抗夾心法ELISA試劑盒,定量檢測(cè)血清、血漿、組織勻漿樣本中的TNFAIP3含量。TNFAIP3 是重要的靶點(diǎn)。它參與細(xì)胞內(nèi)炎癥與免疫調(diào)節(jié)等過(guò)程,可對(duì)腫瘤壞死因子等信號(hào)通路發(fā)揮負(fù)調(diào)控作用。研究其機(jī)制有助于理解免疫相關(guān)疾病發(fā)病機(jī)理,也為開(kāi)發(fā)針對(duì)性治療藥物如抗炎、抗腫瘤藥物提供理論基礎(chǔ)。試劑盒檢測(cè)范圍為23.5 pg/mL-1500 pg/mL,適用于基礎(chǔ)醫(yī)學(xué)研究中探討炎癥相關(guān)疾病機(jī)制、評(píng)估藥物干預(yù)對(duì)TNFAIP3表達(dá)的影響,或解析其在腫瘤微環(huán)境中的調(diào)控作用,為科研人員開(kāi)展免疫調(diào)節(jié)、疾病標(biāo)志物篩選等課題提供可靠工具本品僅用于科研,不用于臨床診斷,產(chǎn)品具體參數(shù)及操作步驟詳見(jiàn)產(chǎn)品說(shuō)明書。
  • 別名:
    A20 ELISA Kit; AISBL ELISA Kit; MGC104522 ELISA Kit; MGC138687 ELISA Kit; MGC138688 ELISA Kit; OTU domain containing protein 7C ELISA Kit; OTU domain-containing protein 7C ELISA Kit; OTUD7C ELISA Kit; Putative DNA binding protein A20 ELISA Kit; Putative DNA-binding protein A20 ELISA Kit; TNAP3_HUMAN ELISA Kit; TNF alpha-induced protein 3 ELISA Kit; TNFA1P2 ELISA Kit; TNFAIP 3 ELISA Kit; TNFAIP3 (A20) ELISA Kit; TNFAIP3 ELISA Kit; Tumor necrosis factor alpha induced protein 3 ELISA Kit; Tumor necrosis factor alpha-induced protein 3 ELISA Kit; Tumor necrosis factor induced protein 3 ELISA Kit; Tumor necrosis factor inducible protein A20 ELISA Kit; tumor necrosis factor, alpha-induced protein 3 ELISA Kit; Zinc finger protein A20 ELISA Kit
  • 縮寫:
  • Uniprot No.:
  • 種屬:
    Homo sapiens (Human)
  • 樣本類型:
    serum, plasma, tissue homogenates
  • 檢測(cè)范圍:
    23.5 pg/mL-1500 pg/mL
  • 靈敏度:
    5.8 pg/mL
  • 反應(yīng)時(shí)間:
    1-5h
  • 樣本體積:
    50-100ul
  • 檢測(cè)波長(zhǎng):
    450 nm
  • 研究領(lǐng)域:
    Immunology
  • 測(cè)定原理:
    quantitative
  • 測(cè)定方法:
    Sandwich
  • 精密度:
    Intra-assay Precision (Precision within an assay): CV%<8%
    Three samples of known concentration were tested twenty times on one plate to assess.
    Inter-assay Precision (Precision between assays): CV%<10%
    Three samples of known concentration were tested in twenty assays to assess.
  • 線性度:
    To assess the linearity of the assay, samples were spiked with high concentrations of human TNFAIP3 in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
     SampleSerum(n=4)
    1:1Average %94
    Range %90-98
    1:2Average %86
    Range %82-92
    1:4Average %95
    Range %89-100
    1:8Average %97
    Range %94-106
  • 回收率:
    The recovery of human TNFAIP3 spiked to levels throughout the range of the assay in various matrices was evaluated. Samples were diluted prior to assay as directed in the Sample Preparation section.
    Sample TypeAverage % RecoveryRange
    Serum (n=5) 8984-94
    EDTA plasma (n=4)9995-103
  • 標(biāo)準(zhǔn)曲線:
    These standard curves are provided for demonstration only. A standard curve should be generated for each set of samples assayed.
    pg/mlOD1OD2AverageCorrected
    15002.496 2.458 2.477 2.344
    7501.658 1.788 1.723 1.590
    3751.085 1.195 1.140 1.007
    187.50.690 0.685 0.688 0.555
    940.454 0.467 0.461 0.328
    470.320 0.321 0.321 0.188
    23.50.231 0.245 0.238 0.105
    00.135 0.131 0.133  
  • 數(shù)據(jù)處理:
  • 貨期:
    3-5 working days

產(chǎn)品評(píng)價(jià)

靶點(diǎn)詳情

  • 功能:
    Ubiquitin-editing enzyme that contains both ubiquitin ligase and deubiquitinase activities. Involved in immune and inflammatory responses signaled by cytokines, such as TNF-alpha and IL-1 beta, or pathogens via Toll-like receptors (TLRs) through terminating NF-kappa-B activity. Essential component of a ubiquitin-editing protein complex, comprising also RNF11, ITCH and TAX1BP1, that ensures the transient nature of inflammatory signaling pathways. In cooperation with TAX1BP1 promotes disassembly of E2-E3 ubiquitin protein ligase complexes in IL-1R and TNFR-1 pathways; affected are at least E3 ligases TRAF6, TRAF2 and BIRC2, and E2 ubiquitin-conjugating enzymes UBE2N and UBE2D3. In cooperation with TAX1BP1 promotes ubiquitination of UBE2N and proteasomal degradation of UBE2N and UBE2D3. Upon TNF stimulation, deubiquitinates 'Lys-63'-polyubiquitin chains on RIPK1 and catalyzes the formation of 'Lys-48'-polyubiquitin chains. This leads to RIPK1 proteasomal degradation and consequently termination of the TNF- or LPS-mediated activation of NF-kappa-B. Deubiquitinates TRAF6 probably acting on 'Lys-63'-linked polyubiquitin. Upon T-cell receptor (TCR)-mediated T-cell activation, deubiquitinates 'Lys-63'-polyubiquitin chains on MALT1 thereby mediating disassociation of the CBM (CARD11:BCL10:MALT1) and IKK complexes and preventing sustained IKK activation. Deubiquitinates NEMO/IKBKG; the function is facilitated by TNIP1 and leads to inhibition of NF-kappa-B activation. Upon stimulation by bacterial peptidoglycans, probably deubiquitinates RIPK2. Can also inhibit I-kappa-B-kinase (IKK) through a non-catalytic mechanism which involves polyubiquitin; polyubiquitin promotes association with IKBKG and prevents IKK MAP3K7-mediated phosphorylation. Targets TRAF2 for lysosomal degradation. In vitro able to deubiquitinate 'Lys-11'-, 'Lys-48'- and 'Lys-63' polyubiquitin chains. Inhibitor of programmed cell death. Has a role in the function of the lymphoid system. Required for LPS-induced production of proinflammatory cytokines and IFN beta in LPS-tolerized macrophages.
  • 基因功能參考文獻(xiàn):
    1. Analysis of postmortem brain tissue and CSF of multiple sclerosis (MS) patients revealed that expression of A20/TNFAIP3, as well as the expression levels of IL-1beta and NLRP3 were significantly increased in MS plaques. PMID: 29789522
    2. LIFR-AS1 serves as a competitive endogenous RNA for miR-29a to inhibit its expression and up-regulate downstream target TNFAIP3 expression, finally modulating the resistance of colorectal cancer to pohotodynamic therapy. PMID: 29807108
    3. Study demonstrates evidence of the constitutive expression of A20 in macrophages, its role in supporting the differentiation program, and the functional consequences of the zinc finger domains thereof. PMID: 28771803
    4. A20 dimers bind linear ubiquitin to stabilize the Ripoptosome and potentiate its apoptosis-inducing activity. PMID: 30209212
    5. At least in the subcutaneous fat of humans and mice, the levels of PGC-1a decrease during obesity, while its physical association with A20 increases. PMID: 29678181
    6. Results suggest a clinicopathologic implication of A20 in progression of NKTL. PMID: 29380463
    7. Studied effect of temperature on gene expression regulation by NF-kappabeta on TNF alpha induced protein 3 (A20) transcription. PMID: 29760065
    8. TNFAIP3 abnormality was less prevalent among intestinal diffuse large B-cell lymphomas with some discordancy between gene deletion and protein expression. PMID: 29463935
    9. antidepressant treatment exerts anti-inflammatory effects, at least in part through increased expression of the TNFAIP3 gene PMID: 27640899
    10. A20 regulates canonical wnt-signaling through an interaction with RIPK4 PMID: 29718933
    11. these results suggested that in human colorectal cancer cells, A20 may function to inhibit cancer progression via down-regulation of TNFalpha-induced chemokine production by suppression of ERK signaling PMID: 29175508
    12. Low A20 expression is associated with HIV disease. PMID: 29505600
    13. A20 overexpression in vivo significantly reduced renal injury as demonstrated by the improved levels of Scr and BUN and the reduction in histological damage. PMID: 29067462
    14. the risk allele for the TNFAIP3 rs2230926 polymorphism was associated with systemic lupus erythematosus susceptibility. PMID: 29783072
    15. It was concluded that the A20 protein in macrophages modulates lung injury induced by LPS. The overexpression of A20 in macrophages may be involved in modulating macrophage polarization. PMID: 28791391
    16. TNF phase III signalling displays ongoing TNFR1/NF-kappa B activation in monocytic cells. High- and low-sensitive genes are induced including differentially regulated A20. A20 strictly controls this signalling in an IKK- and partially RIP-dependent manner. The A20-mediated control mechanisms are supported by ABIN1 and CYLD. PMID: 28629782
    17. A20 is a negative regulator of inflammation in human myometrium and foetal membranes. PMID: 28911210
    18. The tandem polymorphisms (rs148314165, rs200820567), deletion T followed by a T to A transversion and collectively referred to as TT > A variant of TNFAIP3 may be associated with the susceptibility of chronic hepatitis B virus infection but not the clinical disease. PMID: 28784141
    19. elevated A20 expression is involved in the severity of chronic hepatitis B PMID: 28473659
    20. The results of this study confirmed that the A20 expression is reduced in whole blood of Multiple Sclerosis patients as compared to healthy control. PMID: 28337659
    21. C/EBP beta LAP isoform expression was increased and LIP/TNFAIP3/TNIP1 expression was decreased in systemic lupus erythematosus (SLE) patients. LAP expression was positively correlated with SLE disease activity; TNFAIP3 and TNIP1 expression was negatively correlated with SLE disease activity. PMID: 27659348
    22. A20 may have a role in the progression of chronic HBV infection PMID: 27634895
    23. A20 overexpression inhibits hepatic stellate cell activation, which could be the mechanism for high A20 expression protected livers from fibrosis. PMID: 28251449
    24. The data demonstrate that miR-125b regulates nasopharyngeal carcinoma cell proliferation and apoptosis by targeting A20/NF-kappaB signaling pathway, and miR-125b acts as oncogene, whereas A20 functions as tumor suppressor. PMID: 28569771
    25. we demonstrate that a pathological reduction in TNFAIP3 levels induced NF-kappaB/SMAD7 pathway activation, causing a deficiency in MSCs in ITP patients. The ability of ITP-MSCs to support megakaryocytic differentiation and thrombopoiesis of CD34(+) cells was impaired. PMID: 29327472
    26. miR-125b regulates differentiation and reprogramming of T cell glucose metabolism via targeting A20 in T cell acute lymphoblastic leukemia. PMID: 27637078
    27. Review/Meta-analysis: TNFAIP3 gene rs10499194, rs13207033 polymorphisms decrease the risk of rheumatoid arthritis, especially among Caucasian populations. PMID: 27779104
    28. In vitro deletion of A20 in B cells compromised the expression of IL10. PMID: 27825134
    29. Low A20 expression is associated with hepatocellular carcinoma. PMID: 26909601
    30. The results suggest that TNFAIP3 polymorphisms (rs2230926, rs5029937, rs5029939, and rs3757173) are associated with susceptibility to systemic lupus erythematosus. (Meta-analysis) PMID: 27726311
    31. Hepatitis C virus core protein ligates gC1qR to induce A20 expression in macrophages via P38, JNK and NF-kappaB signaling pathways, which leads to a low-grade chronic inflammation during HCV infection. PMID: 27183919
    32. Results show that TNFAIP3 expression is regulated by miR-19b through targeting its 3'-UTR which contributes to the radioresistance of nasopharyngeal carcinoma and consequently activating the NF-kappaB pathway. PMID: 27919278
    33. demonstrates that TNFAIP3 gene polymorphisms (rs2230926 and rs5029937) are associated with the increased risk of rheumatoid arthritis. [META-ANALYSIS] PMID: 28888761
    34. CHN1 and TNFAIP3 are candidate biomarkers for esophageal squamous cell carcinomas PMID: 27072986
    35. These results identify the ubiquitin-editing enzyme A20 as a novel endogenous mechanism for negative regulation of fibrotic response intensity PMID: 27716397
    36. Our data propose an additional novel mechanism to explain the known NF-kappaB inhibitory effects of A20: by affecting p105 ubiquitination and subsequently its degradation and limited processing. PMID: 28923245
    37. A20 promotes metastasis of aggressive basal-like breast cancers through multi-monoubiquitylation of Snail1. PMID: 28892081
    38. Low TNFAIP3 expression is associated with colitis-associated colorectal cancer. PMID: 27991929
    39. The miR-17-92 is a critical contributor to CML leukemogenesis via targeting A20 and activation of NF-kappaB signaling. PMID: 28461114
    40. IM could upregulate A20 protein to inhibit the activation of NF-kappaB pathway in Jurkat T cells, which was independent of the ABIN1 protein. PMID: 28502291
    41. this meta-analysis confirms that TNFAIP3 gene polymorphisms may play important roles in the pathogenesis of Rheumatoid arthritis PMID: 28199970
    42. Report a significant association between the biased usage of IGHV4-34 (binds to the carbohydrate I/i antigens) and inactivating mutation of TNFAIP3 [encoding a global negative regulator of the canonical nuclear factor-kappaB (NF-kappaB) pathway] in ocular adnexal MALT lymphomas. PMID: 28682481
    43. reduced expression confers susceptibility to psoriasis PMID: 28658319
    44. Haploinsufficiency of TNFAIP3 (A20) by a germline heterozygous mutation leads to the autoimmune lymphoproliferative syndrome (ALPS) phenotype. PMID: 27845235
    45. These results suggested that A20 is involved in regulating intracerebral hemorrhage-induced inflammatory injury in both the central and peripheral system PMID: 27986908
    46. In targeted sequencing, a disruptive mutation of TNFAIP3 was the most common alteration (54%), followed by mutations of TBL1XR1 (18%) and cAMP response element binding proteins (CREBBP) (17%). PMID: 28152507
    47. the DNA fragment containing the associated SNPs interacts through chromatin looping not only with TNFAIP3, but also with IL20RA, located 680 kb upstream. PMID: 27799070
    48. The findings suggest that TNFAIP3 protein may be an independent prognostic marker for poor survival, and a promising target for esophageal squamous cell carcinoma therapy. PMID: 28197630
    49. Study demonstrates that the rs7749323 in the TNFAIP3 gene is strongly associated with the late onset myasthenia gravis(with positive AChR Ab but without thymoma). PMID: 28514294
    50. Influenza a virus NS1 has a role in inducing A20 contributes to viral replication by suppressing interferon-induced antiviral response PMID: 27914808

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  • 相關(guān)疾?。?/div>
    Autoinflammatory syndrome, familial, Behcet-like (AISBL)
  • 亞細(xì)胞定位:
    Cytoplasm. Nucleus. Lysosome.; [A20p50]: Cytoplasm.
  • 蛋白家族:
    Peptidase C64 family
  • 數(shù)據(jù)庫(kù)鏈接:

    HGNC: 11896

    OMIM: 191163

    KEGG: hsa:7128

    STRING: 9606.ENSP00000237289

    UniGene: Hs.211600



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