Practical Guidance for Better Laboratory Workflows
These guides address common decisions laboratories face when selecting, implementing, validating, and scaling molecular workflows. Request a guide below, and our team will provide the available information or help you work through the application.
Selecting the Right Nucleic Acid Extraction Kit
Identify the appropriate PureMAGiX chemistry based on sample type, nucleic-acid target, throughput, automation format, and downstream application.
- Sample Type
- DNA or RNA
- Throughput
- Downstream Use
Moving from Manual Extraction to Automation
Evaluate hands-on time, staffing, batch size, run frequency, consumables, validation needs, and the operational impact of automating extraction.
- Labor
- Batch Size
- Automation
- Implementation
Choosing the Right Extraction Platform and Throughput
Compare extraction-platform capacity against current volume, minimum batch size, run frequency, future growth, bench space, and redundancy requirements.
- 16–96 Samples
- Daily Volume
- Capacity
- Growth Planning
Deep-Well Plates, Elution Plates and Tip-Comb Compatibility
Understand plate dimensions, well volume, tip-comb fit, elution formats, sealing, instrument compatibility, and common causes of mechanical workflow problems.
- Deep-Well Plates
- Tip Combs
- Elution Plates
- Instrument Fit
Building an Extraction-to-PCR Workflow
Connect sample preparation, nucleic-acid extraction, elution, PCR setup, controls, amplification, result review, and contamination-control checkpoints.
- Extraction
- PCR Setup
- Controls
- Contamination
Validation and Implementation Planning
Organize intended use, sample types, comparator methods, performance studies, acceptance criteria, training, documentation, and go-live planning.
- Validation
- Acceptance Criteria
- Training
- Go-Live
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