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Human Peroxiredoxin 4(PRDX4) ELISA Kit

  • 中文名稱:
    人氧還原蛋白過氧化物酶4(PRDX4)酶聯(lián)免疫試劑盒
  • 貨號:
    CSB-E13442h
  • 規(guī)格:
    96T/48T
  • 價格:
    ¥3600/¥2500
  • 其他:

產(chǎn)品詳情

  • 產(chǎn)品描述:
    人氧還原蛋白過氧化物酶4(PRDX4)酶聯(lián)免疫試劑盒(CSB-E13442h)為雙抗夾心法ELISA試劑盒,定量檢測血清、血漿樣本中的PRDX4含量。PRDX4 是具有一定生物學(xué)意義的靶點(diǎn)。它在細(xì)胞抗氧化防御等方面發(fā)揮作用。相關(guān)研究聚焦于其參與的信號通路、與疾病發(fā)生發(fā)展的關(guān)聯(lián)機(jī)制,旨在通過揭示其作用原理,為相關(guān)疾病如癌癥等的治療提供新靶點(diǎn)和潛在治療策略。試劑盒檢測范圍為0.625 ng/mL-40 ng/mL,應(yīng)用場景包括但不限于探索氧化應(yīng)激相關(guān)疾病(如神經(jīng)退行性疾病、代謝綜合征)的分子機(jī)制、評估細(xì)胞或動物模型中PRDX4的調(diào)控功能,以及通過血清/血漿樣本分析PRDX4在特定病理生理條件下的生物學(xué)意義。本品僅用于科研,不用于臨床診斷,產(chǎn)品具體參數(shù)及操作步驟詳見產(chǎn)品說明書。
  • 別名:
    Antioxidant enzyme 372 ELISA Kit; Antioxidant enzyme AOE372 ELISA Kit; AOE37 2 ELISA Kit; AOE37-2 ELISA Kit; AOE372 ELISA Kit; EC 1.11.1.15 ELISA Kit; Peroxiredoxin IV ELISA Kit; Peroxiredoxin-4 ELISA Kit; Peroxiredoxin4 ELISA Kit; PRDX 4 ELISA Kit; Prdx4 ELISA Kit; PRDX4_HUMAN ELISA Kit; PRX 4 ELISA Kit; Prx IV ELISA Kit; Prx-IV ELISA Kit; PRX4 ELISA Kit; PrxIV ELISA Kit; Thioredoxin dependent peroxide reductase A0372 ELISA Kit; Thioredoxin Peroxidase (Antioxidant Enzyme) ELISA Kit; Thioredoxin peroxidase ELISA Kit; Thioredoxin peroxidase AO372 ELISA Kit; Thioredoxin-dependent peroxide reductase A0372 ELISA Kit; TRANK ELISA Kit
  • 縮寫:
    PRDX4
  • Uniprot No.:
  • 種屬:
    Homo sapiens (Human)
  • 樣本類型:
    serum, plasma
  • 檢測范圍:
    0.625 ng/mL-40 ng/mL
  • 靈敏度:
    0.156 ng/mL
  • 反應(yīng)時間:
    1-5h
  • 樣本體積:
    50-100ul
  • 檢測波長:
    450 nm
  • 研究領(lǐng)域:
    Cell Biology
  • 測定原理:
    quantitative
  • 測定方法:
    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 PRDX4 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 %88
    Range %84-93
    1:2Average %104
    Range %100-108
    1:4Average %83
    Range %80-86
    1:8Average %94
    Range %91-97
  • 回收率:
    The recovery of human PRDX4 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) 8581-89
    EDTA plasma (n=4)9286-99
  • 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.
    ng/mlOD1OD2AverageCorrected
    402.648 2.609 2.629 2.459
    202.224 2.298 2.261 2.091
    101.545 1.604 1.575 1.405
    50.816 0.835 0.826 0.656
    2.50.531 0.501 0.516 0.346
    1.250.325 0.317 0.321 0.151
    0.6250.241 0.260 0.251 0.081
    00.169 0.171 0.170
  • 數(shù)據(jù)處理:
  • 貨期:
    3-5 working days

產(chǎn)品評價

靶點(diǎn)詳情

  • 功能:
    Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides and as sensor of hydrogen peroxide-mediated signaling events. Regulates the activation of NF-kappa-B in the cytosol by a modulation of I-kappa-B-alpha phosphorylation.
  • 基因功能參考文獻(xiàn):
    1. These features indicate that PRDX4 plays an important role in protecting against liver injury following BDL and might be a promising therapeutic modality for cholestatic diseases. PMID: 30149550
    2. Significant reduction in mRNA and protein levels of PrdxIV was observed in HEK293 cells overexpressing pathologically relevant recombinant mutant GNE protein (D207V and V603L) compared with vector control. Downregulation of PrdxIV keep the ER in a reduced (redox) state that may contribute to misfolding and aggregation of proteins in GNE myopathy. PMID: 28895049
    3. levels of peroxiredoxin 4 are higher in patients with prediabetes, but are similar in subjects with and without insulin resistance, which suggests that the main factor for its increased levels is hyperglycaemia and not insulin sensitivity state. PMID: 27303935
    4. Results show that ERp44 binds the oxidized but not the reduced form of Prx4; the ERp44-Prx4 complex is formed via thiol-disulfide interchange reactions, and its crystal structure reveals a redox-dependent recognition. PMID: 27642162
    5. Prdx4 expression was closely related to follicular development and has aprominent role in protecting human and mouse granulosa cells from reactive oxygen species damage. PMID: 26917265
    6. Positive Prx 4 expression is significantly correlated with recurrence and shorter disease-free survival in patients with early-stage lung squamous cell carcinoma. PMID: 26261544
    7. An off-pathway reaction in the Prx4-mediated oxidative protein folding. PMID: 25137134
    8. Findings suggest that elevated serum Prx4 levels are associated with a higher risk of incident type 2 diabetes PMID: 24893865
    9. Prx4 is a circulating antioxidant and is independently associated with increased risk of cardiovascular and all-cause mortality in T2DM. PMID: 24586984
    10. these data suggest an important role of Prdx4 in maintaining insulin levels and improving the ER folding capacity also under conditions of a high insulin requirement. PMID: 25122762
    11. there is a significant difference in concentration of Prx4 between cardiac arrest patients with good and poor outcome PMID: 24617620
    12. The structure and function of PRDX4 as well as its sensitivity to hyperoxidation. [Review] PMID: 24450625
    13. expression of PRDX4 in PCOS ovaries appeared to be mediated through oxidative stress in GCs. We reported that the deficiency of antioxidant PRDX4 was associated with pathophysiological mechanism of PCOS. PMID: 24098506
    14. peroxiredoxin IV recycling in the endoplasmic reticulum is much less efficient than in the cytosol or mitochondria, leading to the protection of peroxiredoxin IV from hyperoxidation. PMID: 24403061
    15. Remarkably, the Prx4-dependent formation of native disulfide bonds was accelerated when PDI was combined with ERp46 or P5, suggesting that PDIs work synergistically to increase the rate and fidelity of oxidative protein folding. PMID: 23949117
    16. Data indicate that protein disulfide isomerase (PDI) and ERp44 dynamically localize Ero1alpha and peroxiredoxin 4 in early secretory compartment (ESC). PMID: 23979138
    17. expression of Prxs I and IV, both at mRNA and protein levels, was associated with light chain secretion quantified by ELISA. PMID: 23737084
    18. Elevated serum Prx4 levels are associated with a significantly higher risk of incident cardiovascular disease (CVD) events or CVD mortality and all-cause mortality after adjustment for clinical risk factors. PMID: 23316297
    19. these results indicate that two placental proteins, Prx3 and Prx4, may act as new placental immune targets. Production of antibodies against peroxiredoxins 3 and 4 may introduce a new autoimmune hypothesis in recurrent pregnancy loss. PMID: 23190175
    20. data suggest that PRDX4 can be a novel target for glioblastoma multiforme therapies in the future PMID: 22916164
    21. Reverse phase protein arrays verified that the overexpression of both PRDX3 and PRDX4 in prostate tumor samples is negatively correlated with the presence of the TMPRSS2-ERG gene fusion. PMID: 22424448
    22. Prdx4 inhibits G-CSF-induced signalling and proliferation in myeloid progenitors. PMID: 22045733
    23. Overexpression of PRDX4 and P4HA2 was significantly associated with lymphatic metastasis in oral cavity squamous cell carcinoma PMID: 21859152
    24. Crystal structure of reduced and of oxidized peroxiredoxin IV enzyme reveals a stable oxidized decamer and a non-disulfide-bonded intermediate in the catalytic cycle PMID: 21994946
    25. This study solved crystal structures of human Prx4 in three different redox forms and characterized the reaction features of Prx4 with hydrogen peroxide. PMID: 21916849
    26. Data show that Keap1 and PRDX IV were overexpressed in the TNBC cohort. PMID: 21693047
    27. A proteomic approach for identification and localization of the pericellular components of chondrocytes PMID: 21698479
    28. PRDXs exhibit differential expression in prostate tumors, with PRDX3 and 4 consistently upregulated. PMID: 21031435
    29. Elevated serum levels of the antioxidant Prx4 were associated with an increased disease severity and adverse outcome of critically ill patients with sepsis. PMID: 21283059
    30. strong reduction in PRDX4 expression levels in APL correlates with increased trimethylation of histone 3 lysine residue 27 and 4 at the transcriptional start site of PRDX4, indicative of a bivalent histone code involved in transcriptional silencing. PMID: 21283726
    31. Srx-Prx IV axis is critical for lung cancer maintenance and metastasis, suggesting that targeting the Srx-Prx IV axis may provide unique effective strategies for cancer prevention and treatment. PMID: 21487000
    32. PRDX4 has a pivotal protective function against diabetes progression in this type 1 diabetes mellitus model PMID: 20446767
    33. Here, the authors demonstrate that several members of the protein disulphide isomerase family are able to directly reduce this PrxIV disulphide and in the process become oxidized. PMID: 21057456
    34. These results suggest that Prdx-1 and Prdx-4 are essential for preventing respiratory syncytial virus-induced oxidative damage in a subset of nuclear intermediate filament and actin binding proteins in epithelial cells. PMID: 20610706
    35. 2-Cys Prxs act in a mutually nonredundant and sometimes stress-specific fashion to protect human cells from oxidant injury. The substantial resistance of human cells to hydroperoxides may result in part from the additive action of multiple Prxs PMID: 12080185
    36. PRDX4 interacts with and regulates TBXA2R. PMID: 17644091
    37. Peroxiredoxin IV forms complex structures within the ER, consistent with the formation of homodecamers PMID: 18052930
    38. These results suggested that Prx IV involved in the 16alpha-OHE1-induced proliferation of MCF-7 cells has a proliferative effect and may be related to cancer development or progression. PMID: 18272409
    39. data suggested that TRAIL suppressed the PRDX4 gene at the transcriptional level and that downregulation of PRDX4 might facilitate cell death induced by TRAIL PMID: 19364504

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  • 亞細(xì)胞定位:
    Cytoplasm. Endoplasmic reticulum.
  • 蛋白家族:
    Peroxiredoxin family, AhpC/Prx1 subfamily
  • 數(shù)據(jù)庫鏈接:

    HGNC: 17169

    OMIM: 300927

    KEGG: hsa:10549

    STRING: 9606.ENSP00000368646

    UniGene: Hs.83383