CFX96 光学反应模块可将 C1000 Touch™ PCR 仪转换为强大且准确的 CFX96 Touch 荧光定量 PCR 检测系统。 该六通道系统将先进的光学技术与精确温控系统相结合,可进行灵敏而可靠的检测。 在集成的 LCD 触摸屏上快速设置实验并实时监测扩增曲线。 CFX96 Touch 系统多达五个目标基因的检测能力、无出其右的 PCR 仪性能、无可匹敌的独立运行功能以及强大而简单易用的软件,旨在使您的 qPCR 更上一层楼。
主要功能和优点
使用 CFX96 Touch 荧光定量 PCR 检测系统可以:
· 快速设置您的系统 —易于安装且经工厂校准的光学系统
· 尽可能少的样品和试剂使用量 — 使用最低 10 µl 的样品量实现高达 5 目标基因同时检测
· 在一次实验中实现反应体系的优化 — 温度梯度功能
· 更快地分析数据 — 将所有实验数据可视化,并且仅以您要求的格式导出所需数据
· 高级数据分析功能 — 进行归一化处理后给出基因表达分析结果™ 软件规范化基因表达
· 多种方案供您选择 — 可无需电脑操作,在 1 台计算机上最多运行 4 个系统,或与 CFX 自动系统集成以达到更高的通量
· 方便文献的发表 — 包括 MIQE 注释,并使用 Biogazelle 的 qbasePLUS 软件生成 RDML 文件
The CFX96 Touch System is a powerful, precise, and flexible real-time PCR detection system. This six-channel (five colors and one FRET channel) real-time PCR instrument combines advanced optical technology with precise temperature control to deliver sensitive, reliable detection for singlexplex or multiplex reactions.
The CFX96 Touch System is a powerful, precise, and flexible real-time PCR detection system. This six-channel (five colors and one FRET channel) real-time PCR instrument combines advanced optical technology with precise temperature control to deliver sensitive, reliable detection for singlexplex or multiplex reactions.
Key Features and Benefits
With the CFX96 Touch Real-Time PCR Detection System you can:
· Set up your system quickly — easy installation and factory-calibrated optics
· Minimize sample and reagent use — up to 5-target multiplexing with sample volumes as low as 10 µl
· Optimize reactions in a single run — thermal gradient feature
· Analyze data faster — visualize all run data at once and export only the data you need in the format you want
· Use advanced data analysis tools — normalized gene expression using CFX Maestro Software
· Configure the system to fit your needs — run without a computer, run up to 4 systems from 1 computer, or integrate with the CFX Automation System II for higher throughput
· Combine the CFX96 Touch System with good laboratory practice standards — use CFX Maestro Software, Security Edition for data collection and analysis to simplify compliance with U.S. FDA 21 CFR Part 11 regulations