Cellular Imaging
Integra Biosciences Corp HEATMAG MODULE
- Optimized for magnetic bead purification workflows
- Temperature range from ambient to 65 °C
- Exceptional magnet strength for effective separation
- Automated vertical magnet movement
- Adjustable magnet height for various applications
- Integration options: standalone, semi-automated, fully automated
- Compatible with ASSIST PLUS, VIAFLO 96, MINI 96, VIAFLO 384 pipetting platforms
- Accepts 1.5 ml tubes (4 x 6) and 96 well PCR plates
- Key applications include lysis, elution, nucleic acid extraction
- Streamlined molecular biology and proteomics protocols
- Fast and precise bead collection
- Minimal bead carryover
- High yield for purification processes
- Full walk-away automation with ASSIST PLUS
- One-button control for easy operation
Electron Microscopy Sciences Applied Physics LaB6 Cathode for Cameca
Lanthanum hexaboride (LaB6) and cerium hexaboride (CeB6) cathodes are ideal for many small spot size applications such as SEM, TEM, surface analysis and metrology, and for high current applications such as microwave tubes, lithography, electron-beam welders, X-ray sources and free electron lasers. Greater brightness from low work function yielding higher currents at lower temps than tungsten.
Type: LaB6
Angle: 90°
Tips: 16 mm
Type: non-shunted
INTACT GENOMICS INC ig Recombinase Polymerase Amplification (RPA) Kit v1, 25 Reactions
The ig RPA Kit version 1 provides the necessary reagents and enzymes to amplify user-provided DNA template using isothermal Recombinase Polymerase Amplification. It requires no thermocycling with equal or better sensitivity than PCR. RPA is a molecular biology technique that amplifies DNA at a constant temperature using a recombinase, primers, a single-stranded DNA binding protein (SSB), and a strand displacing DNA polymerase. T4 UvsX Recombinase is used with UvsY and primers to cause strand exchange of double-stranded DNA. Then, a single-stranded binding protein, T4 gp32, stabilizes the displaced strand. Finally, Bsu or Sau DNA polymerase extends the DNA from the primers and creates a new complete copy of the template. Iterative amplification ensues as with PCR. RPA is a highly selective and sensitive isothermal amplification technique. No DNA pretreatment is required. It is compatible with a variety of endpoint detection methods, (e.g. lateral flow, real-time fluorescence).