4x2x100ml Swing Buckets Rotor 

Overview

Strong adhesive seal with cross-cut windows. This seal is peelable and suitable for 96 well plates (auto samplers, HPLC, sequencers).

• This strong adhesive seal was developed to facilitate easy sample removal with a manual or automated system
• The seal is optically clear, being made from a transparent polyester film, and has a strong adhesive applied across the underside of the seal, with 96 round windows which align to the 96 wells of a plate
• The optical windows are cross-cut, allowing for easy access to the sample wells with a tip or probe with minimal pressure
• For all adhesive seals, the best sealing results are achieved using our Hand Roller

Strong adhesive seal with cross-cut windows. This seal is peelable and suitable for 96 well plates (auto samplers, HPLC, sequencers).

Cerillo’s Stratus Plate Reader is a third party module that can be placed next to or inside the OT-2 or Opentrons Flex for post experimental analysis. The worktable adapter will allow you to utuilize the OT-2 or Opentrons Flex to prepare the samples directly into the plate reader positions on the worktable.

This small portable device is primarily for microbial growth curve analysis. The Stratus is compatible with Cerillo’s Canopy wireless device that allows real time visualization, control, and analytics. This product is compatible with reading 600nm wavelengths.

Cerillo’s Stratus Plate Reader is a third party module that can be placed next to or inside the OT-2 or Opentrons Flex for post experimental analysis. The worktable adapter will allow you to utuilize the OT-2 or Opentrons Flex to prepare the samples directly into the plate reader positions on the worktable.

This small portable device is primarily for microbial growth curve analysis. The Stratus is compatible with Cerillo’s Canopy wireless device that allows real time visualization, control, and analytics. This product is compatible with reading 600nm wavelengths.

The NGS DNA Fragmentation & Library Prep Kit (ion torrent platform) was developed for construction of high quality libraries for next generation sequencing for ion torrent platform. The kit uses intact genomic DNA (both EDTA-free DNA and DNA in TE buffer are compatible) as input DNA without an additional DNA fragmentation step. Our NGS kit has a fast and simple workflow with only three step. In addition,  all steps can be performed in one tube. The DNA libraries can be generated within one hour with less than 10 minutes of  hands-on time. Library multiplexing up to 12 samples is possible.

NGS DNA Fragmentation & Library Prep Kit Workflow

The incorporation of DNA fragmentation in the kit makes it possible to directly use intact genomic DNA as input DNA without the need of mechanical DNA shearing or enzymatic DNA fragmentation. The protocol is optimized to generate libraries from 200 bp to 500 bp in size. The library size is inversely correlated with the incubation time of step 1 at 20°C.

Kit features:

• • • Fast: 1-hour library construction from intact genomic DNA to NGS library
    • • Total time: 1 hr
      • Hands-on time: 5 min
    • Intact genomic DNA can be used directly as input; DNA fragmentation is not required.
    • Works with both EDTA-free DNA samples and DNA samples in TE buffer
    • Simple workflow
    • • Three steps
      • Only one beads purification step
    • Guaranteed quality: high library conversion efficiency based on our chemistry

Library conversion efficiency for NGS DNA Fragmentation & Library Prep Kit (Ion Torrent Platform). 100 ng, 300 ng and 500 ng of DNA were used as input.

NGS DNA Fragmentation & Library Prep Kit (Ion Torrent Platform): Library size distribution with different incubation time.

The NGS DNA Fragmentation & Library Prep Kit (ion torrent platform) was developed for construction of high quality libraries for next generation sequencing for ion torrent platform. The kit uses intact genomic DNA (both EDTA-free DNA and DNA in TE buffer are compatible) as input DNA without an additional DNA fragmentation step. Our NGS kit has a fast and simple workflow with only three step. In addition, all steps can be performed in one tube. The DNA libraries can be generated within one hour with less than 10 minutes of hands-on time. Library multiplexing up to 12 samples is possible.