MultiNA II MCE-301, Microchip Electrophoresis System for DNA/RNA Analysis - Features

Microchip Electrophoresis System

Simple and Smart Workflow

Designed with the user in mind, MultiNA II delivers efficient, reliable analysis using simple, streamlined operations. Its intuitive software guides users through clear, automated workflows, significantly increasing laboratory productivity.

Reliability

STEP 1  Reliability 
Register analysis schedule

Because sample racks can be removed from the instrument for handling, samples can be registered while ensuring proper handling. The software enables easy selection of analysis sequences and allows users to save, import, and export schedules for added flexibility.

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Operating

 

STEP 2  Operating Efficiency 
Place samples and reagents

Simply place the samples and reagents in the tray, insert the tray into the system, and start the analysis.

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Operating

STEP 3  Operating Efficiency 
Click the start button

All —from sample dispensing to microchip rinsing— are performed automatically by the system. Data is displayed in real time, starting with the sample currently being analyzed, allowing results to be reviewed immediately.

Convenience

Checking Analysis Results  Convenience 

Intuitive data analysis software enables instant confirmation of key target information.

Novel Functionality Achieves a New Workflow

workflow

 

Automated Sample Dilution

Samples can be diluted with purified water to ensure the concentration is within the quantifiable range. The system can automatically dilute samples to the specified concentration level (5, 10, or 20-fold dilution)*1.

*1 Dilution functionality is supported for up to 48 samples. Tubes for dispensing diluted samples are required separately.

Adding samples

Adding Samples During Analysis

The system can be paused during an analysis to allow adding up to 120 samples. This is particularly useful when analyzing samples from multiple users because there is no need for the analyst to prepare all the samples at the same time or wait until the current analysis is finished.

images

 

Changing the Order of Gel Images

Gel images can be rearranged into any order, regardless of the original sample analysis.

Past Data

 

Comparison/Analysis of Past Data

Past data can be displayed next to current data for easy comparison. Even data acquired using a previous model (MCE-202 MultiNA) can be loaded and analyzed*2.

*2 Data analysis is not supported for some reagent kits.

Operating

 Operating Efficiency 

Automatic Analysis Significantly Shortens Analysis Time

Analysis can begin after just 10 minutes of preparation. Fully automated operation significantly reduces hands-on time, while overnight analysis capabilities free up valuable time for research and other business activities.

Reliability

 

 Reliability 

Calibration Curves Used for Automatic Prediction

Predicted fragment sizes and concentrations are calculated automatically, providing objective, quantitative results. Each analysis is normalized using an internal standard reagent to ensure reliable data.

Convenience

 

 Convenience 

Convenience of Using Data

Dedicated data analysis software incorporates powerful, purpose-built tools that make it easier to process, interpret, and act on data across a wide range of applications.

Enhanced Analysis Functions

RNA

RNA Integrity Index (RII)

Because extracted RNA begins degrading the moment it is isolated, reliable quality assessment is essential. MultiNA systems provide a built-in solution for computing RII values as an independent indicator of RNA quality. With a coefficient of determination of 0.95 or higher compared to integrity indices from non-Shimadzu platforms, MultiNA delivers confidence and compatibility you can trust.

Enhanced Analysis Function

 

RNA Integrity Index

 

  • mRNA Analysis: Used for Purity Analysis

    Cas9 mRNA (4522 nt) and EPO mRNA (859 nt) mixtures prepared to 4:1, 10:1, 20:1, and 100:1 concentration ratios were analyzed using the MultiNA. The EPO mRNA was clearly detectable for all ratios.

  • mRNA

     

DNA

DNA Fingerprinting Analysis

For analysis with a positive control, the presence/absence of a specific DNA fragment in samples can be determined automatically. After analysis, results can be collectively listed or shown grouped with other samples of the same type.

  • DNA

    Tuna PCR-RFLP Patterns

  • DNA

    Tuna Discrimination Patterns

User-Friendly Design

Intuitive Software

In addition to rearranging gel images, it is easy to display size prediction values as size guides (red lines) within gel images or electropherograms.

Intuitive Software

 

  • Removable Sample Rack

    This removable rack holds up to 96 plates. Up to 2 types of reagent kits can be loaded in a mixed arrangement.

  • Removable Sample Rack

     

Expandable Application Range

Genome Editing

Grouping and molar concentration ratio analysis provide powerful support for fast, reliable screening of genome-edited samples.

Detection of Deletion Mutations Induced by Genome Editing Tools

Genome-editing technologies have transformed the ability to precisely modify biological organisms, driving rapid growth in research that relies on these tools. The heteroduplex mobility assay (HMA) offers a fast, simple, and cost-effective method to assess whether genome edits have been successfully introduced. Because heteroduplex DNA migrates more slowly during electrophoresis, HMA enables rapid mutation detection and straightforward genotype determination.

Genome Editing

 

  • Grouping Analysis Analytical Intelligence

    Correlation coefficient values are calculated from heteroduplex mobility assay results, enabling automatic grouping of samples with the same mutation type. This allows reliable, automated discrimination between homo and hetero types, which can be presented in a single, easy-to-review list, a task that previously relied on subjective visual interpretation.

  • Grouping Analysis

     

  • Molar Concentration Ratio Analysis

    By defining a target size range, the system calculates the molar concentration ratio of peaks (bands) within that range. This enables quantitative evaluation of mutation activity for the designed genome-editing tool using data from HMA, Cel-I assays, PCR-RFLP, and other analysis methods.

  • Molar Concentration Ratio Analysis

     

Analytical Intelligence

Analytical Intelligence is a new concept for analytical devices offered by Shimadzu. It ensures systems and software are operated just like an experienced expert would, by automatically determining whether the system status and results are acceptable or not and by providing feedback to users and resolving problems. It also ensures data reliability by compensating for any differences between user instrument knowledge or experience levels.

NGS

With the high-sensitivity kit, smear analysis functionality, and RNA integr

NGS Library Quality Control

Successful NGS starts with a well-characterized library. The smear analysis feature delivers precise average size and concentration measurements, ensuring a clear understanding of library quality. When paired with the high-sensitivity kit, it enables confident evaluation of libraries at concentrations as low as 5 pg/μL—supporting dependable performance even with low-input samples.

NGS Library Quality Control

 

  • High-Sensitivity Kit

    Achieve precise, reliable evaluation of library data using the newly released DNA High-Sensitivity Kit.

  • High-Sensitivity Kit

Genotyping

Built-in DNA fingerprinting capability enables fast, accurate, and effortless genotype identification.

Determining the Type of Meat Products

Meat identification based on appearance and texture can be misleading, particularly for processed or less-fresh products.
Using a genetic analysis workflow combining PCR with restriction enzyme digestion overcomes this challenge, enabling confident, highly accurate determination of meat species.

Determining the Type of Meat Products

 

ECO Functions, Energy Savings

MultiNA II uses 30% less power than its predecessor and is 27% shorter, making it an effortless fit even in compact lab environments. In addition, rinsing now uses 75% of the purified water compared to the previous model, representing a significant reduction in liquid waste to support more sustainable laboratory operations.

Energy Savings Achieved

Comparison of Power Consumption by MultiNA II and Previous Model

Energy Savings Achieved

Power consumption has been reduced to 70 % of the previous model, lowering operating costs during analysis and contributing to reduced carbon emissions.

Water Savings

Purified Water Consumption by MultiNA II Compared to Previous Model

Water Savings

The purified water consumption for rinsing has been reduced to 75% of the previous model's level, significantly reducing liquid waste and lowering the system's overall environmental impact.

Requires Less Space

 

Requires Less Space

The MultiNA II has a 15 % smaller footprint and is 27 % shorter than the previous model (with the front door open), making it easier to install and freeing up valuable bench space.

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