Products & Reviews

Generate N1-methyl-pseudouridine-containing mRNA (N1meΨ-mRNA) with greatly reduced double-stranded RNA (dsRNA) content. Easily remove dsRNA without the need for chromatographic methods like HPLC. Produce large amounts of N1meΨ-mRNA with virtually 100% transcript capping. Induce lower innate immune response in mammalian cells.

Remove cap structures (decapping) from various RNAs. Substitute unit for unit into any prexisting protocol for Tobacco Acid Pyrophosphatase (TAP).

Optimized for precision, flexibility, and hypoxic workflows.

Build Cap 0 or Cap 1 caps with nearly 100% efficiency. Provides all reagents for capping in vitro transcribed RNA.

Prepare Cap 1-RNA from any source of Cap 0-RNA. Use simultaneously with ScriptCap™ m7G Capping System to produce virtually 100% Cap 1-capped RNA in a single reaction.

Made for the LUNA-BX7™ and LUNA-FX7™ automated cell counters, the disposable LUNA™ 1-, 3-, and 8-chamber slides provide higher throughput options effectively increasing measuring volume and lowering CV.

Generate pseudouridine-containing mRNA (Ψ-mRNA) with greatly reduced double-stranded RNA (dsRNA) content. Easily remove dsRNA without the need for chromatographic methods like HPLC. Produce large amounts of Ψ-mRNA with virtually 100% transcript capping. Induce lower innate immune response in mammalian cells.

Specially formulated for maximum yields of canonical (GAUC) in vitro transcribed RNA. Produce up to 180 µg of RNA from 1 µg of template in just 30 minutes. Easily scale up reactions to produce milligram amounts of RNA.

The LUNA-BX7™ offers an affordable high performance automated cell counter with brightfield optics only. It’s a top tier high throughput cell counter with compliance capabilities at a budget-friendly price. Based on the footprint of the award-winning LUNA-FX7™, the LUNA-BX7™ is equipped with the same small footprint, state of the art optics, advanced software, and features including daily quality control and compliance.

Optimized for high-yield synthesis of 5-methyl-cytidine- pseudouridine-containing, in vitro transcribed RNA (5mCΨ-RNA). Produce up to 100 µg of 5mCΨ-RNA from 1 µg of template in 2 hours. Easily scale up to produce milligram amounts of 5mCΨ-RNA. Induce lower innate immune responses in mammalian cells by using 5mCΨ-mRNAs.

For a more eco- and user-friendly dye option, Erythrosin B Stain is a nontoxic and safe vital dye used to assess cell viability.

Used in fluorescence cell counting, Acridine Orange/Propidium Iodide Stain (AO/PI), Acridine Orange Stain (AO), and Propidium Iodide Stain (PI) are used to assess cell viability. Acridine Orange/Propidium Iodide Stain causes viable nucleated cells to fluoresce green and nonviable nucleated cells to fluoresce red.

Advanced detection for complex assays

One-touch, end-to-end workflow for every lab.

Quantitative mRNA poly(A) tail length using standard polyacrylamide gel electrophoresis (PAGE). Easy, cost-effective benchtop method for QC as an alternative to mass spec analysis. Assess tail lengths above the limits of HPLC and LC-MS based methods.

Streamlining magnetic bead purifications

Quantitate mRNA capping efficiency (percent capped RNA content) of XBG 5’ UTR-containing mRNA using standard polyacrylamide gel electrophoresis (PAGE). XBG 5’ UTR Targeting Oligonucleotide and XBG 5’ UTR Control Mix included in kit. Easy, cost-effective, benchtop method useful for QC as an alternative to HPLC and LC-MS analysis.

Easy to use, scalable enzymatic method for removing double-stranded RNA (dsRNA) from RNA samples. Remove dsRNA without the need for chromatographic methods like HPLC. No reduction in single-stranded RNA (ssRNA) yields. Reduces the innate immunogenic response to mRNA in cells.

Powerful Urine Sediment Imaging, Now in a Smaller Size. Advanced digital microscopy for accurate urine sediment analysis, in a reduced footprint

Cryopreserved, highly reproducible patient-derived organoids ready for immediate use

Inhibits eukaryotic RNases A, B and C. Use as a safeguard against RNA degradation in any RNA-containing reaction.

LUMOS II ILIM redefines infrared imaging speed and precision. With patented Infrared Laser Imaging technology, it delivers hyperspectral data at a pace that transforms workflows: what used to take months can now be done in days. It’s not just faster—it’s smarter, combining automation, AI-driven analysis, and multimodal imaging for research and routine applications alike.

Optimized for high-yield synthesis of pseudouridine-containing, in vitro transcribed RNA (Ψ-RNA). Produce up to 100 µg of Ψ-RNA from 1 µg of template in 2 hours. Induce lower innate immune responses in mammalian cells by using Ψ-mRNA.

All-in-one kit to produce N1-methyl-pseudouridine-containing-mRNA (N1meΨ-mRNA). Combine the benefits of high-yield transcription with post-transcriptional capping and tailing. Produce large amounts of N1meΨ-mRNA with virtually 100% transcript capping. Induce lower innate immune response in mammalian cells by using N1meΨ-mRNAs.

Drug testing made simple.