Your cart is empty.
无论是想定量少量DNA或RNA样本,还是整合自动化工作流程进行质控,帝肯都有相应的解决方案来满足客户的需求。
核酸提取后或作为NGS工作流程的一部分进行定量和均一化,可以避免由于样品不足或污染导致的质量不良或下游失败,节省时间和降低成本。
***************************************************************************************
***************************************************************************************
Tab 01 / 独立的DNA和RNA定量
***************************************************************************************
***************************************************************************************
Infinite 200 PRO多功能酶标仪系列在一个袖珍的仪器中提供吸光度和高灵敏度荧光读取模式。 它结合了荧光分析的高灵敏度和方便的无标记紫外分析可满足高达384孔板的分析。
阅读更多内容Infinite M Nano酶标仪是广受赞誉的Infinite 200 PRO的六种新定制配置之一, 为DNA和RNA提供高灵活度的快速定量,从试管到384孔板。
Quad4 Monochroors™专利技术基于230- 1000nm的完整光谱分析,让您对样本质量完全有信心。
阅读更多内容NanoQuant Plate™专利技术代表了市场上最准确和可重复的微量核酸定量工具,适用于少到2µl的样本。 其高精度的石英光学保证了同时测量多达16个样本的优异性能,且无需校准。与所有帝肯多功能酶标仪兼容,这个强大的工具对DNA/RNA的定量和小体积样本的质控近似完美。
阅读更多内容
***************************************************************************************
***************************************************************************************
Tab 02 / 整合定量与和均一化
***************************************************************************************
***************************************************************************************
用于Fluent工作站的Frida Reader模块可以在不损失样品的情况下对核酸进行定量。该设计模块与Fluent工作站的Air Flexible Channel Arm™ (AirFCA)结合使用。该专利方法基于紫外吸收对悬滴中的核酸进行的定量和纯度评估,避免核酸纯化(NAP)后稀有和珍贵样本的损耗。它是珍贵或微量样本的理想选择,因为样本被吸回到枪头,可以直接用于进一步处理,例如均一化。
下载更多Frida Reader信息DNA定量可以用荧光染料(如PicoGreen®或QuantiFluor™)测定, 或测量整个DNA样本的吸光度来实现。
DNA定量和均一化工作流程通常包括以下步骤:
Freedom EVOware®均一化程序是一个软件组件,可高效地对核酸样本进行自动化移液定量和均一化。
将不同浓度的样本在整个微孔板上稀释至均一浓度。这使Freedom EVO工作站能够执行样本均一化任务所需的所有移液和微孔板处理步骤。
阅读更多内容使用几个简单的命令来执行定量和均一化的复杂任务,可以节省时间。
***************************************************************************************
***************************************************************************************
Tab 03 / 整合片段分析
***************************************************************************************
***************************************************************************************
传统上,DNA片段的质量分析是通过琼脂糖凝胶电泳进行的,既费时又费力。
来自Advanced Analytical的片段分析仪INFINITY(FAI)提供自动化多通道毛细管电泳,可满足96个样本的并行高分辨率分离。
它可以准确地对核酸片段和涂片从50bp到50kb进行长度分析和定量,并可以兼容两种不同的凝胶试剂,在应用程序和样本类型之间无缝切换。
有20多个试剂盒可供选择--每个试剂盒都为分析不同的片段长度而优化--用于:
将FAI集成到Freedom EVO®液体处理平台上,可以将重要的质控检查点整合到自动化基因组学流程中。
允许更长的无人值守时间,确保DNA片段符合后续测序或其他下游分析所需的质控标准。
Freedom EVO上整合全自动DNA质控的片段分析仪INFINITY
Tecan Labwerx™ 可以将FAI集成到Freedom EVO工作站的右侧,允许系统的机械臂灵活访问。这种配置为访问FAI侧板、补充凝胶、调整液体和清空废瓶提供了方便。
有关硬件和软件整合的更多信息,请参阅相关的 技术说明 。
***************************************************************************************
***************************************************************************************
Tab 04 / 文献
***************************************************************************************
***************************************************************************************
Accurate nucleic acid quantification and quality control without sample loss
Module for Fluent® automation workstation specifications and typical performance values
Software to help you normalize your DNA samples to uniform concentration
Nucleic acid quantification and normalization is required in most genomics workflows, most commonly after the initial nucleic acid purification step, but consumes precious sample and can be tedious when performed manually. The versatility of the classical UV absorbance-based technique still makes it the ‘go to’ method for many applications, as it allows the concentration of all DNA and RNA types to be measured (based on the specific empirical extinction coefficient for each nucleic acid type) and provides simultaneous assessment of samples for impurities that could impair downstream applications.
The Frida Reader is an add-on module for the Fluent Automation Workstation that revolutionizes the way quantification and normalization are performed. It allows samples to be measured in a hanging drop at the end of a disposable pipette tip, completely eliminating sample loss for nucleic acid quantification.
DNA quantification and normalization are critical steps for a wide range of genomics applications, such as next generation sequencing and quantitative PCR. Due to the limitations of classical absorbance techniques, a number of more sensitive methods for quantification of double stranded DNA (dsDNA) have been developed over the years. Fluorescence-based techniques have proved popular with researchers, as the introduction of fluorescent dsDNA-binding dyes with minimal binding to single stranded DNA (ssDNA) and RNA allows selective quantification of even small amounts of dsDNA.
Applicability of the NanoQuant PlateTM for Fluorescence Measurements.
Absorbance measurement on the Infinite® M200 microplate reader using the NanoQuant Plate™.
NanoQuant Plate™ for use on Infinite® F200 and Infinite® M200
Straightforward automation on the Tecan Freedom EVO®
Quantification and normalization of double stranded DNA with minimal set-up time.
Fast and simple DNA quantification and normalization
Fluorescence intentsity on Infinite™ F200 an Infinite M200.
Comparing absorbance measurements between the Quad4 Monochromators™-based Infinite® M200 PRO and a multimode reader using photodiode array technology.
NanoQuant Plate™ for use of Infinite® 200 NanoQuant.
Automated QC analysis for NGS Library Preparation and CRISPR/CAS9 Gene Editing
The Frida Reader for Fluent offers UV-based concentration and purity measurements of nucleic acid samples in a hanging drop at the end of a disposable tip. This patented method is completely free of sample loss, as the hanging drop is aspirated back into the tip, and can be used for further processing (e.g. a normalization). No additional preparation steps, labware or reagents are required for the measurement, which offers precision and accuracy comparable to a reference reader over a range of 2 to 1,000 ng/μl.