<dd id="fncnt"><pre id="fncnt"></pre></dd>

  • 細胞凋亡EpiTect甲基化PCR檢測芯片 Apoptosis EpiTect Methyl qPCR Array

    科技服務 > 生物芯片實驗服務 > 細胞凋亡EpiTect甲基化PCR檢測芯片 Apoptosis EpiTect Methyl qPCR Array

    細胞凋亡EpiTect甲基化PCR檢測芯片 Apoptosis EpiTect Methyl qPCR Array

    細胞凋亡EpiTect甲基化PCR檢測芯片Apoptosis EpiTect Methyl qPCR Array
    運費 ¥0.00
    (庫存 9999 件)

     
    Apoptosis EpiTect Methyl qPCR Array 細胞凋亡DNA甲基化PCR芯片
     
    ProductSpeciesTechnologyCat. No.
    Apoptosis EpiTect Methyl qPCR ArrayHumanDNA MethylationEAHS-121Z
    Apoptosis EpiTect Methyl qPCR ArrayMouseDNA MethylationEAMM-121Z
    Apoptosis EpiTect Methyl qPCR ArrayRatDNA MethylationEARN-121Z
     
    The Apoptosis EpiTect Methyl II Signature PCR Array profiles the promoter methylation status of a panel of 22 promoters of genes involved in apoptosis, or programmed cell death. Dysregulation of apoptosis, leading to uncontrolled cell growth, is a hallmark of carcinogenesis. Hypermethylation of pro-apoptotic genes (BNIP3L) silences their expression, which can lead to tumor progression. Profiling cellular or fresh tissue genomic DNA samples with these arrays may help correlate CpG island methylation status with biological phenotypes. The results may also help provide further insights into the role dysregulated apoptosis plays in diseases such as cancer. With a simple restriction enzyme digestion and real-time PCR, research studies can analyze the promoter methylation status of 22 different apoptosis genes with this DNA methylation PCR array.
    Both 96-well and 384-well ( 4 X 96 ) formats are available
    細胞凋亡EpiTect甲基化PCR芯片是一款檢測甲基化狀態的芯片,檢測的包括涉及凋亡或程序性死亡的22個基因的啟動子甲基化狀態。細胞凋亡失調從而導致不可控的細胞生長是典型的致癌標志。甲基化可使促凋亡基因 (BNIP3L) 沉默,從而導致腫瘤的發生。用這些基因陣列分析細胞或新鮮組織基因組DNA樣本有助于分析生物表型下的CpG島甲基化狀態。結果也可以為細胞凋亡異常在癌癥等疾病中的作用提供進一步的見解。用一個簡單的限制性內切酶消化和實時PCR, 通過這個DNA甲基化PCR芯片可以分析22個不同的細胞凋亡基因的啟動子甲基化狀態。有96和384(4 X 96) 兩種型號。
    Induction of Apoptosis:BAD, BAX, BCL2L11, BCLAF1, BID, BIK, BNIP3L, CASP3, CIDEB, CRADD, DAPK1, DFFA, FADD, GADD45A, HRK, LTBR, TNFRSF21, TNFRSF25 (DR3), TP53.
    Anti-Apoptosis:BAX, BNIP3L, DAPK1, HRK.
    Regulation of Apoptosis:
    Negative Regulation:BIRC2, BNIP3L, CASP3, DAPK1, DFFA, TP53.
    Positive Regulation:BAD, BAX, BCL2L11, BCLAF1, BID, BIK, BNIP3L, CIDEB, CRADD, FADD, HRK, TNFRSF25 (DR3), TP53.
    Caspases & Regulators:APAF1, BAX, CASP3, CASP9, CRADD, TP53
     

    The EpiTect Methyl II PCR Array System is a fast, reliable technology that profiles the DNA methylation status of a panel of genes. These PCR Arrays can help you discover and verify cancer or developmental biomarkers useful for both basic and applied research. No bisulfite conversion is required, and the challenges of real-time PCR primers design and optimization has already been done for you. EpiTect Methyl II PCR Arrays are ideal for fast, high-throughput methylation analysis. For determining the exact methylation level of individual and consecutive CpG sites, we recommend using bisulfite Pyrosequencing on a PyroMark system.

     

    How it Works 工作原理與流程

    The EpiTect Methyl II PCR Array System relies on the differential cleavage of target sequences by two different restriction endonucleases whose activities require either the presence or absence of methylated cytosines in their respective recognition sequences. As real-time PCR quantifies the relative amount of DNA remaining after each enzyme digestion, the methylation status of individual genes and the methylation profile across a gene panel are reliably and easily calculated. The high yield of DNA from the restriction digests and PCR amplification allow the analysis of smaller, more heterogeneous samples.

    Download User Manual  Tour the FREE Data Analysis Template

    What It Offers:

    • Guaranteed Performance - Ready-to-use for DNA methylation analysis

    • Time & Cost Savings - Less than 30 min hands-on time to analyze up to 94 genes

    • Easy Data Analysis - FREE Excel-based data analysis template available

    You can easily perform an EpiTect Methyl II experiment in your own laboratory using any 96-well or 384-well real-time PCR instrument that you have access to.
    Or you can send your DNA samples to us and take advantage of our 
    PCR Array Services.

    Array Layout:
    The PCR Arrays are available in both 96- and 384-well plate formats to analyze the methylation status of 22 or 94 genes related to a disease state, such as specific types of cancer, or development pathways related to specific cells or tissues. The Signature panels of 22 genes are arranged on either 96-well or 384-well plates to simultaneously characterize all four restriction digests from either one or four different DNA samples, respectively. The more Complete panels of 94 genes are arranged on 96- or 384-well plates to characterize all four restriction digests from one DNA sample either on four plates or all on the same plate, respectively.

    For more detail on PCR Array layout, see the "Gene Table" link for the individual array products.

    Data Interpretation
    EpiTect Methyl II PCR Arrays provide gene methylation status as percentage unmethylated (UM) and percentage methylated (M) fraction of input DNA. "UM" represents the fraction of input genomic DNA containing no methylated CpG sites in the amplified region of a gene. "M" represents the fraction of input genomic DNA containing two or more methylated CpG sites in the targeted region of a gene. The number of CpG sites methylated in a targeted region can vary within the fraction of methylated input DNA.

    In the figure above, each horizontal bar represents the targeted region of a gene from one genome. Biological samples usually contain many genomes derived from many cell types. For simplicity, five such genomes are depicted here. Light and dark circles represent unmethylated and methylated CpG sites, respectively.

    Performance Data

    To verify the reliability of the EpiTect Methyl II PCR Array System, its results and sensitivity were compared with bisulfite Sanger sequencing, the gold standard in DNA methylation analysis

    Same Results as Bisulfite Sanger Sequencing

    To validate the reliability of the system, EpiTect Methyl II PCR system results (EpiTect Methyl II PCR) were compared with bisulfite Sanger sequencing, the gold standard in DNA methylation analysis. The methylation status of the cadherin 13 (CDH13) gene promoter was analyzed using either bisulfite sequencing or EpiTect Methyl II PCR Assays in two different cell lines. EpiTect Methyl II PCR Assays revealed that 100% of total input DNA had methylated CDH13 gene promoter in MB231 cell lines whereas 100% of input DNA from HeLa cell line had unmethylated CDH13 promoter. Importantly, EpiTect Methyl II PCR Assays yielded results similar to Bisulfite Sequencing.

    Same Sensitivity as Bisulfite Sanger Sequencing

     

    Primary tumors are typically very heterogeneous, containing a mixture of both cancerous and noncancerous cells. Therefore, reliable tumor characterization requires detecting smaller amounts of methylated DNA diluted in an unmethylated background. To test the sensitivity of EpiTect Methyl II PCR system to detect methylated DNA diluted in an unmethylated background, SKBR3 breast cancer cell line and normal blood genomic DNA (encoding methylated and unmethylated HIC1, respectively) were mixed in different ratios. EpiTect Methyl II Human HIC1 PCR Primers Assays were used to detect the methylation status of the mixed sample. Result show that the percentage of methylated HIC1 relative to total promoter DNA in each mixture was detectable even down to six percent of the total DNA sample showing the high sensitivity of EpiTect Methyl II PCR system.

    Application Data

    Gene promoter methylation is the most common epigenetic mechanism silencing tumor suppressor genes during oncogenesis. Almost all cancer-related signaling pathways are affected by methylation, and the number of genes affected in each major type of cancer is still rapidly growing. However, even the most relevant genes have not yet been correlated to individual cancer types or subtypes in order to better define biological pathways and mechanisms leading to oncogenesis and in order to properly develop DNA methylation biomarkers. The EpiTect Methyl II PCR System provides an ideal reagent for such studies, without bisulfite conversion of DNA. The following experiments demonstrate that EpiTect Methyl II PCR Arrays can both verify known and discover new DNA methylation cancer biomarkers

    EpiTect Methyl II PCR Arrays are used to screen Breast Cancer Gene Methylation Status in Breast Cancer Cell Lines.The heat map compares the methylation status of 22 genes in the genomic DNA of three breast cancer cell lines and blood genomic DNA (used as an unmethylated control) determined with the Human Breast Cancer EpiTect Methyl II Signature PCR Arrays. The results further strengthen the correlation of these biomarkers with breast cancer.

    Biomarker / Pathway Discovery
    Cancer progresses through aberrant cell differentiation due to alterations in gene expression. Transcription factors regulate gene expression, and many tumor suppressor genes and oncogenes, defined by classical genetic methods, encode transcription factors. Does the methylation status of transcription factor genes differ between cancer and normal cells?

    EpiTect Methyl II DNA Methylation PCR Arrays Discover New Candidate Breast Cancer DNA Methylation Biomarkers. The heat map compares the methylation status of a panel of 79 transcription factor genes in six different breast cancer cell lines (some in duplicate) and a normal epithelial cell line as determined using 384-well EpiTect Methyl II Custom PCR Arrays. These breast cancer cell lines also methylate this gene panel potentially providing a new source of cancer biomarkers.

    These results are consistent with the notions that aberrant expression of transcription factors controlling cell differentiation plays key roles in oncogenesis and that transcription factors can be tumor suppressors.


    姓名
    電話號碼
    電子郵箱
    公司名稱
    地址
    留言*
     
    驗證碼
    提交
    999国产精品永久免费视频,free性朝鲜娇小videos,亚洲高清国产拍精品26u,东北女人毛多水多牲交视频