产品封面图

细胞凋亡miRNA PCR芯片 Apoptosis miSc

ript miRNA PCR Array
收藏
  • 询价
  • 美国
  • Apoptosis miScript miRNA PCR Array细胞凋亡miRNA PCR芯片
  • 2026年01月19日
    avatar
  • 企业认证

    点击 QQ 联系

    • 详细信息
    • 文献和实验
    • 技术资料
    • 服务名称

      Apoptosis miScript miRNA PCR Array细胞凋亡miRNA PCR芯片

    • 提供商

      SAbiosciences

    “英拜助您实验加速”
    Apoptosis miScript miRNA PCR Array细胞凋亡miRNA PCR芯片
    Apoptosis miScript miRNA PCR Array细胞凋亡miRNA PCR芯片
    Product Species Technology Cat. No.
    Apoptosis miScript miRNA PCR Array Human miRNA Expression MIHS-114Z
    Apoptosis miScript miRNA PCR Array Mouse miRNA Expression MIMM-114Z
    Apoptosis miScript miRNA PCR Array Rat miRNA Expression MIRN-114Z
    The Apoptosis miScript miRNA PCR Array profiles the expression of 84 miRNAs that regulate programmed cell death by inhibiting pro-apoptotic and anti-apoptotic gene expression. This array provides researchers with a convenient way to quickly analyze the miRNAs most relevant to apoptosis. Apoptosis plays a critical role in normal biological processes requiring cell removal including differentiation, development, and homeostasis. Stress responses (such as heat shock, ischemia, unfolded proteins, and viral infection) cause badly damaged cells to undergo apoptosis. In cell culture, growth factor withdrawal and many known experimental compounds have a similar effect. An acquired defect in apoptosis activation often leads to uncontrolled cell growth, oncogenesis, and cancer. Ligand-bound tumor necrosis factor (TNF) receptors initiate apoptosis by recruiting FADD and other death domain adaptor proteins that then recruit and activate caspases. Environmental stresses trigger BCL2 protein oligomerization and insertion into the mitochondrial membrane, releasing APAF1 and other CARD family members that also oligomerize to recruit and activate caspases. Caspases promote a proteolytic cascade that degrades cellular protein targets, while the IAP protein family directly inhibits caspases. Besides these post-translational events, miRNAs provide another mechanism of regulating apoptosis by attenuating gene expression. This array represents miRNAs experimentally verified to regulate many pro- and anti-apoptotic genes and to stimulate or attenuate apoptosis upon their overexpression or inhibiton. Monitoring their expression helps determine the mechanisms behind programmed cell death in any model system and the propensity of a cell type to undergo apoptosis normally. A set of controls present on each array enables data analysis using the ΔΔCT method of relative quantification, assessment of reverse transcription performance, and assessment of PCR performance. Using SYBR® Green real-time PCR, the expression of a focused panel of miRNAs related to apoptosis can be easily and reliably analyzed with this miScript miRNA PCR Array.
    miScript miRNA PCR Arrays are intended for molecular biology applications. This product is not intended for the diagnosis, prevention or treatment of a disease
    细胞凋亡miRNA PCR芯片检测84个通过抑制凋亡激活和抗凋亡基因来调节细胞程序性死亡的microRNA的表达。这个芯片为研究人员提供了一个方便的方法来快速分析与细胞凋亡相关的microRNA。凋亡细胞在正常生物过程中起着至关重要的作用,包括分化、发育和内稳态的调节。应激反应(如热休克、缺血,展开的蛋白质,和病毒感染)引起严重受损的细胞发生凋亡。在细胞培养中生长因子消退和许多已知的实验化合物也有相似的效果。后天的细胞凋亡激活缺陷往往导致不可控的细胞生长,肿瘤形成,和癌症。配体肿瘤坏死因子(TNF)受体启动细胞凋亡通过招募FADD和其他死亡结构域接头蛋白,然后招募和激活凋亡蛋白酶。环境压力引发BCL2蛋白质的寡聚化和插入到线粒体膜,释放APAF1和其他寡聚化的CARD家族成员,来招募和激活凋亡蛋白酶。凋亡蛋白酶促进蛋白质级联水解,来降解细胞蛋白质,而IAP蛋白质家族直接抑制凋亡蛋白酶。除了这些翻译后调控,microRNA提供另一种衰减基因表达来调节细胞凋亡的机制。这个芯片的microRNA在实验上已证实,来调控许多促进和抑制凋亡的基因,通过过表达或抑制来促进或减弱凋亡。检测他们的表达有助于确定细胞程序性死亡背后的机制在任何模型系统和经细胞凋亡过程的细胞类型倾向。每个芯片上有一组对照组,其数据分析可使用ΔΔCT相对量化的方法,评估逆转录性能和聚合酶链反应性能的评估。使用SYBR®GREEN实时PCR和microrna qPCR芯片,可以很容易地、可靠地分析与细胞凋亡有关的miRNA。
    miScript microrna的PCR芯片用于分子生物学的应用程序。本产品不用于诊断,预防和治疗的疾病。
    Anti-Apoptotic:miR-106b-5p, miR-141-3p, miR-183-5p, miR-186-3p, miR-210, miR-214-3p, miR-338-3p, miR-378a-3p, miR-98-5p, miR-133a, miR-181a-5p, miR-21-5p, miR-25-3p, miR-30a-5p, miR-30b-5p, miR-30d-5p.
    Pro-Apoptotic:miR-128, miR-143-3p, miR-144-3p, miR-200c-3p, miR-205-5p, miR-206, miR-212-3p, miR-218-5p, miR-26a-5p, miR-26b-5p, miR-27a-3p, miR-30c-5p, miR-30e-5p, miR-31-5p, miR-365a-3p, miR-409-3p, miR-449a, miR-708-5p, let-7c, let-7g, miR-1, miR-101-3p, miR-133b, miR-149-3p, miR-153, miR-15b-5p, miR-16-5p, miR-181b-5p, miR-195-5p, miR-203a, miR-204-5p, miR-29a-3p, miR-29c-3p, miR-34a-5p, miR-497-5p, miR-512-5p.
    Either Anti-Apoptotic or Pro-Apoptotic:let-7e-5p, miR-23a-3p, miR-24-3p, miR-34c-5p, let-7a-5p, miR-29b-3p.
    Targets Anti-Apoptotic Genes:let-7c, let-7g, miR-1, miR-101-3p, miR-122-5p, miR-133a, miR-133b, miR-193b, miR-194-5p, miR-204-5p, miR-491-5p, miR-512-5p, miR-542-3p, miR-7-5p, miR-9-5p.
    Targets Pro-Apoptotic Genes:miR-134, miR-221-3p, miR-222-3p, miR-32-5p.
    Targets Both Anti-Apoptotic & Pro-Apoptotic Genes:let-7a-5p, miR-125a-5p, miR-125b-5p, miR-1285-3p, miR-145-5p, miR-146a-5p, miR-149-3p, miR-153, miR-15a-5p, miR-15b-5p, miR-16-5p, miR-17-5p, miR-181a-5p, miR-181b-5p, miR-181c-5p, miR-181d, miR-185-5p, miR-192-5p, miR-193a-5p, miR-195-5p, miR-203a, miR-20a-5p, miR-21-5p, miR-25-3p, miR-29a-3p, miR-29b-3p, miR-29c-3p, miR-30a-5p, miR-30b-5p, miR-30d-5p, miR-34a-5p, miR-451a, miR-497-5p, miR-92a-3p

    实验原理与流程

    产品细节图片1

    What miScript miRNA PCR Arrays offer?
    Guaranteed Performance* - ready-to-use for gene expression analysis
    Time & Cost Saving - less than 30 min hands-on time to analyze 84 or 372 miRNA
    Simple Data Analysis - easy-to-use Excel-Based Data Analysis Template

    风险提示:丁香通仅作为第三方平台,为商家信息发布提供平台空间。用户咨询产品时请注意保护个人信息及财产安全,合理判断,谨慎选购商品,商家和用户对交易行为负责。对于医疗器械类产品,请先查证核实企业经营资质和医疗器械产品注册证情况。

    图标文献和实验
    相关实验
    • micro RNA(miRNA)

      的小分子――筛选一定大小的RNA分子,连接到3'和5'的适配子(adapters),逆转录并通过PCR扩增、亚克隆并测序。miRNA前体在基因组上的定位和聚类是通过向基因组数据库查询进行。这个方法有助于判断miRNAs是否是mRNAs、tRNAs、rRNAs等分子的降解产物。 有的实验室通过一种RNA folding program 'mfold'来判断C. elegans和C. briggsae之间的高度保守区域是否含有潜在的miRNA前体,然后用Northern Blots的方法来确定

    • miRNA的靶基因的寻找与鉴定

      miRNA靶基因的验证与miRNA靶基因 的预测方法相比,对miRNA靶基因进行实验验证的方法并不多,目前还没有一个快速、简便、高通量的鉴定方法。最直接的鉴定方法是, 利用荧光定量PCR及Westernblot方法分别检测转染或敲低miRNA后细胞中mRNA水平及蛋白水平的变化,从而确定miRNA与靶基因的对应关系。这种方法能够直接鉴定出miRNA的靶基因, 准确度高但不能鉴定miRNA的靶位点。转染或敲低miRNA:方式主要有两种,一种是构建miRNA过表达载体的稳定表达系统,一种是人工合成miRNA

    • 【求助】miRNA芯片数据分析问题

      。一般是做6张可以了。但是还要有后继实验的啊,比如real time pcr,进行验证芯片结果。做几十例,然后做统计。 要是配对的样本做配对T检验,但先做F检验,看是正态还是偏态分布。然后选择合适的统计方法。 以上是个人意见。 lide658 你好:我也曾经做过PCR-array芯片,首先我觉得你实验组和对照组各做3张完全可以计算P值,其次一般认为有差异的倍数是3倍,若是条件放宽一点,2倍的也可以入选。对于结果分析方面,有些公司

    图标技术资料

    需要更多技术资料 索取更多技术资料

    同类产品报价

    产品名称
    产品价格
    公司名称
    报价日期
    询价
    上海英拜生物科技有限公司
    2026年01月20日询价
    询价
    上海杏园瑞民生物工程有限公司
    2025年08月26日询价
    ¥5000
    上海伯豪生物技术有限公司
    2026年01月16日询价
    询价
    上海吉凯基因医学科技股份有限公司
    2026年01月18日询价
    询价
    上海芯超生物科技有限公司
    2025年12月24日询价
    细胞凋亡miRNA PCR芯片 Apoptosis miScript miRNA PCR Array
    询价