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  4. Human G1/S-specific cyclin-E1(CCNE1) ELISA kit

Human G1/S-specific cyclin-E1(CCNE1) ELISA kit

  • 中文名稱：
    人G1/S特異性細(xì)胞周期蛋白E1(CCNE1)酶聯(lián)免疫試劑盒
  • 貨號(hào)：
    CSB-EL004817HU
  • 規(guī)格：
    96T/48T
  • 價(jià)格：
    ￥3600/￥2500
  • 其他：

產(chǎn)品詳情

  • 產(chǎn)品描述：

    This Human CCNE1 ELISA Kit was designed for the quantitative measurement of Human CCNE1 protein in serum, plasma, tissue homogenates, cell lysates. It is a Sandwich ELISA kit, its detection range is 25 pg/mL-1600 pg/mL and the sensitivity is 6.25 pg/mL.

  • 別名：
    CCNE ELISA Kit; Ccne1 ELISA Kit; CCNE1_HUMAN ELISA Kit; cyclin E variant ex5del ELISA Kit; cyclin E variant ex7del ELISA Kit; Cyclin E1 ELISA Kit; Cyclin Es ELISA Kit; Cyclin Et ELISA Kit; CyclinE ELISA Kit; G1/S specific cyclin E ELISA Kit; G1/S-specific cyclin-E1 ELISA Kit
  • 縮寫：
  • Uniprot No.：
  • 種屬：
    Homo sapiens (Human)
  • 樣本類型：
    serum, plasma, tissue homogenates, cell lysates
  • 檢測范圍：
    25 pg/mL-1600 pg/mL
  • 靈敏度：
    6.25 pg/mL
  • 反應(yīng)時(shí)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 CCNE1 in various matrices and diluted with the Sample Diluent to produce samples with values within the dynamic range of the assay.
    　 Sample Serum(n=4)
    1:1 Average % 100
    Range % 95-104
    1:2 Average % 95
    Range % 90-100
    1:4 Average % 91
    Range % 86-95
    1:8 Average % 84
    Range % 80-88
  • 回收率：
    The recovery of human CCNE1 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 Type Average % Recovery Range
    Serum (n=5) 93 89-97
    EDTA plasma (n=4) 88 84-92
  • 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/ml OD1 OD2 Average Corrected
    1600 1.921 1.837 1.879 1.741
    800 1.294 1.228 1.261 1.123
    400 0.819 0.783 0.801 0.663
    200 0.543 0.519 0.531 0.393
    100 0.362 0.376 0.369 0.231
    50 0.280 0.301 0.291 0.153
    25 0.207 0.194 0.201 0.063
    0 0.141 0.135 0.138 　
  • 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：
    Essential for the control of the cell cycle at the G1/S (start) transition.
  • 基因功能參考文獻(xiàn)：
    1. miR-874 inhibits CCNE1 expression during growth factor deprivation and that miR-874 down-regulation in osteosarcomas leads to CCNE1 up-regulation and more aggressive growth phenotypes. PMID: 29109143
    2. Amplified/cyclin E1(hi) and non-amplified/cyclin E1(hi) tumors have different pathological and biological characteristics and clinical outcomes indicating that they are separate subsets of cyclin E1(hi) HGSOC. PMID: 30209015
    3. Breast cancer recurrence-free interval was significantly worse in patients with cyclin E (LMW-E)-positive tumors who received aromatase inhibitor (AI) neoadjuvant therapy, compared with those with LMW-E negative tumors. PMID: 28947566
    4. in a series of human biopsies, non-metastatic SCCs displayed a higher degree of chromosomal alterations and higher expression of the S phase regulator Cyclin E and the DNA damage signal gammaH2AX than the less aggressive, non-squamous, basal cell carcinomas. However, metastatic Squamous cell carcinoma lost the gammaH2AX signal and Cyclin E, or accumulated cytoplasmic Cyclin E. PMID: 28661481
    5. Cytoplasmic cyclin E identifies patients with the highest likelihood of recurrence consistently across different patient cohorts and subtypes. These patients may benefit from alternative therapies targeting the oncogenic isoforms of cyclin E. PMID: 27881578
    6. our results validate the assumption that CBX7 is a tumor suppressor of gliomas. Moreover, CBX7 is a potential and novel prognostic biomarker in glioma patients. We also clarified that CBX7 silences CCNE1 via the combination of CCNE1 promoter and the recruitment of HDAC2. PMID: 28460453
    7. Our findings suggest that gene copy-number gain and upregulation of CCNE1 occur in ovarian clear cell carcinoma and are associated with a worse clinical outcome, dictating the survival of early-stage patients. PMID: 27767100
    8. YAP/ TAZ pathways contribute to the proliferation/quiescence switch during colon cancer 5FU treatment according to the concerted regulation of Cyclin E1 and CREB PMID: 27527859
    9. Silencing of CDCA5 suppresses proliferation of gastric cancer cells by inducing G1-phase arrest via downregulating CCNE1. PMID: 29326043
    10. Analysis of genomic data from TCGA demonstrated coamplification of CCNE1 and AKT2 Overexpression of Cyclin E1 and AKT isoforms, in addition to mutant TP53, imparted malignant characteristics in untransformed fallopian tube secretory cells, the dominant site of origin of high-grade serous ovarian cancer PMID: 27663592
    11. Finding suggest that amplification of CCNE1 serves as one mechanism for the development of some serous tubal intraepithelial carcinomas. PMID: 27443516
    12. Prognostic gene sets based on the 13 genes were developed, and their prognostic values were verified in three independent patient cohorts (n=501). Among them, a signature of CCNE1 and its coexpressed genes was significantly associated with disease progression and validated in the independent cohorts. PMID: 28082741
    13. Cyclin E1 mRNA and protein expressions were suppressed. PMID: 26603262
    14. The opposing effects of ORC1 (represor) and CDC6 (gene activator) in controlling the level of Cyclin E ensures genome stability and a mechanism for linking directly DNA replication and cell division commitment. PMID: 27458800
    15. High cyclin E expression is associated with breast cancer. PMID: 28760857
    16. High CCNC1 expression is associated with inflammatory breast cancer. PMID: 28107181
    17. Inhibition of cell division cycle associated 2 (CDCA2) suppressed the proliferation of lung adenocarcinoma (LAC) cells via G1 phase arrest by downregulating cyclin E1(CCNE1), while overexpression of CDCA2 promoted LAC cells proliferation by upregulating CCNE1. PMID: 28423619
    18. a PI3K/PKCiota/cyclin E signaling pathway as a therapeutic target during ovarian tumorigenesis PMID: 26279297
    19. Amplification of 19q12 CCNE1/URI was found in 10.4% (28/270) and was significantly associated with type II endometrial cancer (EC) high grade, advanced FIGO stage, and aberrant tumor supressor p53 expression. PMID: 27582547
    20. Results show that cyclin E1 and CDK2 participate in STC1 promoting cell proliferation of prostate neoplasm cells. PMID: 28350121
    21. cyclin E is specifically dephosphorylated at S384 by the PP2A-B56 phosphatase, thereby uncoupling cyclin E degradation from cyclin E-CDK2 activity PMID: 28137908
    22. These results provide evidence that ARTD1 regulates cell cycle re-entry and G1/S progression via cyclin E expression and p27(Kip 1) stability independently of its enzymatic activity, uncovering a novel cell cycle regulatory mechanism. PMID: 27295004
    23. These results demonstrate a repressor role for NFAT1 in cell cycle progression and Cyclin E expression in B lymphocytes, and suggest a potential function for NFAT1 protein in B cell malignancies. PMID: 27399331
    24. High CCNE1 amplification and expression is associated with breast cancer. PMID: 26810187
    25. CCNE1/REL gene interaction might play pivotal roles in the occurrence and development of Postmenopausal Osteoporosis. PMID: 26676054
    26. These results indicate that miR-25 has anti-apoptosis roles in AGS cells, possibly via inhibiting FBXW7 and thus promoting oncogenes, such as CCNE1 and MYC. PMID: 27120728
    27. Cyclin E-driven OvCa cells appeared addicted to glucose metabolism via TCA. Combined CDKi with modalities targeting TCA, like SDHA inhibition showed promising effects for this genotype. Combined blockade of CDK and SDH, both genetically and pharmaceutically, showed synergy and resulted in inhibited proliferation, migration, invasion and migration in A2780 cells PMID: 26826064
    28. Over-expression of CCNE1 is associated with non-small cell lung cancer. PMID: 26771237
    29. High levels of cyclin E are a predicator of poor prognosis among patients with gastrointestinal cancer. [meta-analysis] PMID: 25627202
    30. The effects of CCNE1 knockdown were dependent on the CCNE1 expression status. PMID: 26647729
    31. Data show that melanoma antigen, family C, 2 protein (MAGE-C2) binds with RING-box protein 1 (Rbx1) and Cullin 1, and regulates cyclin E stability in melanoma cells. PMID: 26540345
    32. The findings suggest that the role of cyclin E and tumor specific low molecular weight isoforms as mediators of tumorigenesis is in part dependent on p53 context. PMID: 26625764
    33. Ad-cycE can target cyclin E overexpression in cancer cells and repress tumor growth in syngeneic mouse models. PMID: 26475304
    34. ovary tumors with elevated CCNE1 expression may be staged for Cdk2-targeted therapy PMID: 26204491
    35. our findings identify a novel mechanism of cyclin E-mediated Mcl-1 regulation in human cancer PMID: 26219338
    36. miR-15b might be involved in termination of osteoblastic cells proliferation by arresting them at G0/G1 phase through direct targeting cyclin E1. PMID: 26007664
    37. A significant correlation between cyclin E1 amplification and deletions at a number of the genomic loci in breast cancer. PMID: 25959964
    38. These results indicate cyclin E1 is downregulated by both miR-497 and miR-34a, which synergistically retard the growth of human lung cancer cells. PMID: 25909221
    39. MicroRNA-30c-2-3p negatively regulates NF-kappaB signaling and cell cycle progression through downregulation of TRADD and CCNE1 in breast cancer. PMID: 25732226
    40. Results show that miR-16 and HuR co-regulate the cyclin E1 mRNA without influencing each other's binding or expression. miR-16 regulation predominates, blocking upregulation of cyclin E1 by HuR. PMID: 25830480
    41. Expression of Notch1, -2, and -3, CDK2, and CCNE1 was significantly decreased by upregulation of ALDH1A1 in A549 cells, but increased by its interruption in A549s cells. PMID: 24671051
    42. Results show that CCNE1 and BRD4 on chromosome 19 were amplified/overexpressed in a substantial cases of epithelial ovarian cancer with no involvement of BRCA genes. PMID: 25892415
    43. This study indicates that CCNE1 rs1406 polymorphism may contribute to BC risk PMID: 25159285
    44. Suppression of NF90 caused a decrease in the half-life of cyclin E1 mRNA PMID: 25399696
    45. miR-144-5p functions as tumour suppressor in BC cells. CCNE1 and CCNE2 were directly regulated by miR-144-5p and might be good prognostic markers for survival of bladder cancer patients PMID: 26057453
    46. HOXA7 promotes cell proliferation, and these changes are mediated by cyclin E1/CDK2 PMID: 25501982
    47. Aurora-A/HURP relays cell transforming signal to NF-kappaB, and the HURP/NF-kappaB complex is engaged in the regulation of cyclin E1 expression. PMID: 25289861
    48. Contrary to previous literature, we found a correlation between cyclin E expression and prognosis. Further large-scale studies are required to confirm our findings. PMID: 26026100
    49. Global gene expression profiling identifies ALDH2, CCNE1 and SMAD3 as potential prognostic markers in upper tract urothelial carcinoma. PMID: 25408144
    50. The cell cycleassociated proteins cyclin E and p27kip1 may have contributed to this antitumor effect. PMID: 25310086

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  • 亞細(xì)胞定位：
    Nucleus.
  • 蛋白家族：
    Cyclin family, Cyclin E subfamily
  • 組織特異性：
    Highly expressed in testis and placenta. Low levels in bronchial epithelial cells.
  • 數(shù)據(jù)庫鏈接：

    HGNC: 1589

    OMIM: 123837

    KEGG: hsa:898

    STRING: 9606.ENSP00000262643

    UniGene: Hs.244723