Cambio - Excellence in Molecular Biology

Strip Out dsRNA. Unlock True mRNA Performance.

• Boosts mRNA performance to higher translation efficiency.
• Reduce dsRNA to below assay LLOQ (<0.005%).
• Simple, scalable enzymatic workflow
• Compatible with all IVT mRNAs.
  

Engineered for clean, confident amplification.

Activate hot-start precision the moment speed matters.

From cloning to food borne pathogen detection this be the Taq you have been waiting for.

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Full range of swabs now available 

• Forensics + Genetics
• Diagnostics + Specimen Collection
• Environmental
• Medical 

Benchtop PAGE mRNA QC is the New LC/MS

Perform precise quantitative mRNA 5’ capping efficiency and 3’ poly(A) tail length assessments using standard lab equipment

Available in CytoOrange, CytoGreen or CytoAqua.

We offer the full range of Cytotest Probes. Just contact us for details.

New 10CFU and 100CFU Mycoplasma Standards are here:

Fully compliant with EP 2.6.7

Cambio Ltd:-

• Use 100% renewable electricity 
• Reuse, reduce or repurpose as much of our packaging as possible
• Have been recycling polystyrene boxes for over 40 years   
• Are supporting our local bio diversity especially bees and butterflies in recycled pallets used as planters
• Offset our equivalent carbon footprint making contributions to The Woodland Trust.

You read about our continued efforts in the sustainability statement here 

Rapid Micronucleus MoA Test Kit for detection of Micronuclei, Clastogens, Aneugens and other chromosomal aberrations

Fast Identification of micronuclei (MN), nucleoplasmic bridges (NPBs) and nuclear buds (NBUDs) as markers of chromosomal instability and aberration

Easily detect one of the unseen enemies

Venor® Bacteria qPCR enables rapid detection of bacterial contamination in cell cultures and ATMPs.

• Time-to-result: < 3 hours
• QC release testing of ATMPs and other short-shelf life products
• Detects 95% of bacteria including VBNCs

Perfect replacement for tobacco acid pyrophosphatase

• Remove 5’ cap structures (decapping) from various RNAs, including mRNA.
• Substitute unit-for-unit in any preexisting protocol using Tobacco Acid Pyrophosphatase (TAP).