Cellular Imaging Instrumentation Accessories
Molecular Devices Objective 20x S Plan Fluor ELWD, 0.45 NA
Objective 20x S Plan Fluor ELWD, 0.45 NA.
Molecular Devices Genomic Filter Slide, 260/280/320 nm, 10 nm Bandwidth
The Molecular Devices Genomic Filter Slide is a multi-filter slide for filter-based microplate readers, built for genomic absorbance measurements and nucleic acid quantitation. It contains narrow-band UV filters that enable accurate 260/280 ratio assessments for nucleic acid purity.
- Contains filters centered at 260 nm, 280 nm, and 320 nm.
- 10 nm bandwidth for each filter.
- Designed for genomic absorbance and nucleic acid quantitation.
- Fits standard filter-slide mounts on compatible microplate readers.
- Enables reliable measurement of nucleic acid purity via 260/280 ratios.
Molecular Devices Nikon Objective, CFI S Plan Fluor ELWD, 60X, 0.7 NA
60X extra-long working distance objective with 0.70 numerical aperture, optimized for fluorescence and brightfield imaging. The correction collar accommodates variable cover glass thickness and the extended working distance suits thick samples and culture vessels.
- 60x magnification with 0.70 numerical aperture.
- Extra-long working distance for imaging thick samples.
- Correction collar for 0.1-1.3 mm cover glass thickness.
- Air immersion, spring-loaded objective design.
- Suitable for fluorescence and brightfield applications.
- Compatible with high-content imaging and live-cell workflows.
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).
INTACT GENOMICS INC ig Recombinase Polymerase Amplification (RPA) Kit v1, 500 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).
INTACT GENOMICS INC ig Recombinase Polymerase Amplification (RPA) Kit v1, 100 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).