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- 详细信息
- 文献和实验
- 技术资料
- 服务名称:
人癌症药物靶标ChIP qPCR芯片
- 提供商:
SAbiosciences
技术服务网址:http://www.yingbio.com/
服务热线:400-696-6643、 18019265738
邮箱:daihp@yingbio.com 、 huizhang1228@foxmail.com
Cancer Drug Targets EpiTect ChIP qPCR Array
人癌症药物靶标ChIP qPCR芯片
| Product | Species | Technology | Cat. No. |
| Cancer Drug Targets EpiTect ChIP qPCR Array | Human | Histone Modifications | GH-507A |
| Cancer Drug Targets EpiTect ChIP qPCR Array | Mouse | Histone Modifications | GM-507A |
The Human Cancer Drug Targets EpiTect Chip qPCR Array profiles the histone modification status or “histone code” of 84 actively sought targets for anticancer therapeutics and drug development. Histone modifications define chromatin structure, and some correlate closely with the transcriptional activity of associated genes.In vitro screening of therapeutics for a given cancer type increasingly depends on not only the activity, but also the expression and epigenetic status of oncogenes. For example, histone deacetylase (HDAC) inhibitors induce tumor suppressor gene expression, slowing growth and proliferation, but could also increase oncogene expression. The choice to add HDAC inhibitors to a drug regimen can depend on the histone codes of the two gene classes. Cancer cells with oncogenes in a heterochromatin state may respond better to HDAC inhibitor treatment because these genes would not be expressed or easily induced. Comprehensively understanding how oncogenes contribute to tumor growth and survival on the molecular level requires a determination of the epigenetic mechanisms regulating their expression. Using chromatin immunoprecipitation and this real-time PCR Array, you can easily and reliably analyze the histone modification patterns associated with a focused panel of important cancer-related genes.
人癌症药物靶标ChIP qPCR芯片用于分析抗癌疗法和药物开发积极寻求的84个靶标的组蛋白修饰状态或组蛋白密码。组蛋白修饰调节染色质结构和与转录活性相关的基因。体外筛选癌症疗法对于一个给定的类型不仅越来越多地依赖于活性,还依赖致癌基因的表达和表观遗传状态。例如组蛋白脱乙酰酶(HDAC)抑制剂引起肿瘤抑制基因表达,生长和增殖减缓,但也可能增加致癌基因表达。可以根据两类组蛋白编码基因,选择添加HDAC抑制剂到给药方案。癌细胞在癌基因异染色质状态下可能对HDAC抑制剂治疗反应更好,因为这些基因不表达或容易诱导。全面了解致癌基因在分子水平上促进肿瘤的生长和生存需要一个确定的调节他们表达的表观遗传机制。通过染色质免疫沉淀和EpiTect ChIP qPCR芯片,可以很简易可靠地分析组蛋白的化学修饰模式与重要癌症相关基因的表达。
Apoptosis:BCL2, BIRC5.
PI-3 Kinases & Phosphatases:FRAP1 (MTOR), PIK3C2A, PIK3C3, PIK3CA.
Growth Factors & Receptors:EGFR, ERBB2, ERBB3, ERBB4, FIGF, FLT1, FLT4, IGF1, IGF1R, IGF2, KDR, KIT, PDGFRA, PDGFRB.
Drug Metabolism:ABCC1, GSTP1, PTGS2, TXN, TXNRD1.
G Protein Signaling:RHOA, RHOB.
Hormone Receptors:ESR1, ESR2, PGR.
Heat Shock Proteins:HSP90AA1, HSP90B1.
Receptor Tyrosine Kinase Signaling:AKT1, AKT2, GRB2.
Cathepsins:CTSB, CTSD, CTSL1, CTSS.
Cell Cycle:CDC2, CDC25A, CDK2, CDK4, CDK5, CDK7, CDK8, CDK9, MDM2, MDM4, TERT.
Topoisomerases, Type II:TOP2A, TOP2B.
Transcription Factors:ATF2, HIF1A, IRF5, NFKB1, TP53.
Protein Kinases:AURKA, AURKB, AURKC, PLK1, PLK2, PLK3, PLK4, PRKCA, PRKCB, PRKCD, PRKCE.
RAS Signaling:HRAS, KRAS, NRAS.
Histone Deacetylases:HDAC1, HDAC11, HDAC2, HDAC3, HDAC4, HDAC6, HDAC7, HDAC8.
Poly ADP-Ribose Polymerases:PARP1, PARP2, PARP4, TNKS.
Structural Protein:NTN3.
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文献和实验基因芯片技术及其应用 基因芯片(DNA Chip) 又称DNA 芯片、DNA 微阵列等等,是伴随人类基因组计划而产生的,是近年来分子生物学及医学诊断技术的重要进展。该技术的突出特点在于其高度的并行性、多样化、微型化、自动化,被认为是生命科学研究中继基因克隆技术、基因自动测序技术、PCR 技术后的又一次革命性 的技术突破[1 ] 1 基因芯片技术简介 基因芯片将半导体工业的微型制造技术与分子生物学技术结合起来,通过把巨大数量的寡核苷酸、肽核酸或cDNA 固定在一块面积极小的硅片、玻片
ChIP‐Seq: A Method for Global Identification of Regulatory Elements in the Genome
binding regions in mammalian cells by ChIP: Comparison of array‐ and sequencing‐based technologies. Genome Res. 6:898‐909. The ENCODE Project Consortium. 2007. Identification
功能的研究提供了强有力的工具,将会使基因诊断、药物筛选、给药个性化等方面取得重大突破,该技术被评为1998年度世界十大科技进展之一。1、基本概念基因芯片(gene chip)也叫DNA芯片、DNA微阵列(DNA microarray)、寡核苷酸阵列(oligonucleotide array),是指采用原位合成(in situ synthesis)或显微打印手段,将数以万计的DNA探针固化于支持物表面上,产生二维DNA探针阵列,然后与标记的样品进行杂交,通过检测杂交信号来实现对生物样品快速、并行、高效
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