SP-NE32 FAQs

MGISP-NE32

SP-NE32 - Frequently Asked Questions

What are the main differences between SP-NE32, SP-100B and SP-960?

SP-NE32 uses a magnetic rod method with pre-filled reagents and supports 32 samples. SP-100B and SP-960 use pipetting-based liquid handling, with SP-960 offering higher throughput up to 192 samples.

It uses magnetic rods to move magnetic beads that bind nucleic acids, enabling automated capture, washing and elution while removing impurities.

It uses magnetic rods to move magnetic beads that bind nucleic acids, enabling automated capture, washing and elution while removing impurities.

They use pipette tips for liquid transfer and mixing, offering flexible workflows and integration with automated PCR system construction.

All systems support automated nucleic acid extraction, while SP-100B and SP-960 also support automated PCR system setup.

It supports a wide range of samples including tissue, blood, plasma, faeces and swabs, suitable for downstream applications like qPCR and sequencing.

It uses UV sterilisation, disposable consumables and pre-packaged reagents to minimise cross-contamination and ensure safe operation.

The system processes up to 32 samples per run using two reagent plates, each handling 16 samples.

SP-NE32 uses magnetic rod sleeves and pre-filled reagent plates, while SP-100B and SP-960 use pipette tips and tube-based reagents.

It holds multiple certifications including NMPA, CE-IVD, CE-RUO and CB, demonstrating compliance with international safety and performance standards.