Dual tag
cost-effective
site-selective
robust
How does it work?
Dual Tag:
simultaneous5' end and3'end labeling
independent and selective modification
Orthogonal labeling:
fluorescent dyes, biotin and reactive chem. groups
RNA toolbox:
one-pot protocol
Simple and Reliable
up to 99% for oligoRNA
up to 85% for mRNA
High yields:
~100€ per gram of RNA
Cost-effective:
with dually labeled RNA
Correct protein expression
for in vitro and in vivo studies
RNA probes
multicolor img., fret, pull-down, bioconjugation and more...
Suitable for
ND
~50 000 €
~7 000 000 €
~422 000 €
RNA toolbox and labeling technologies
Dual tag
to study its distribution, accumulation, transcription, degradation and more...
Dual Tag
simultaneous 5' end and 3'end labeling
independent and selective modification
Orthogonal labeling:
fluorescent dyes, biotin and reactive chem. groups
RNA toolbox:
up to 99% for oligoRNA
up to 85% for mRNA
High yields:
Cost-effective:
~100€ per gram of RNA
with dually labeled RNA
Correct Protein Synthesis
one-pot protocol
Simple and reliable
multicolor img., fret, pull-down, bioconjugation and more...
Suitable for
5'end labeling
3'end labeling
Dual Tag
Pierce RNA 3'Kit
5' EndTag Kit
ND
High yield for <100n
Min. translation yield loss
Correct protein synthesis
High yield for >1000n
Reagents cost per gram
(in 1000 €)
50
7 000
422
For more than three decades, we have been leading advancements in gene therapy, focusing on improving mRNA stability. Our contributions are crucial in addressing cancer and genetic diseases, and have achieved commercial success worldwide, benefiting major companies like BioNTech, Sanofi, and Genentech.
Enhanced mRNA Stability Method
(applied in multiple clinical trials)
US20100233757
2010
mRNA Cap Analog Technology
(utilized in advanced genetic vaccine development)
US20110092574
2010
mRNA Modification for Increased Protein Synthesis
EP2502938A1
2011
Efficient mRNA Delivery System
WO2012149280A1
2012
mRNA-Based Cancer Vaccine Platform
US20130115294A1
2013
For more than three decades, we have been leading advancements in gene therapy, focusing on improving mRNA stability. Our contributions are crucial in addressing cancer and genetic diseases, and have achieved commercial success worldwide, benefiting major companies like BioNTech, Sanofi, and Genentech.
mRNA Modification for Increased Protein Synthesis
EP2502938A1
2011
Efficient mRNA Delivery System
WO2012149280A1
2012
mRNA-Based Cancer Vaccine Platform
US20130115294A1
2013
Enhanced mRNA Stability Method
(applied in multiple clinical trials)
US20100233757
2010
mRNA Cap Analog Technology
(utilized in advanced genetic vaccine development)
US20110092574
2010
>80 publications
>1500 citiations
28 H-Index
The main co-author
Ph.D. at Max Planck Institute of Biochemistry
Assistant professor at University of Warsaw
>140 publications
>2550 citiations
34 H-Index
Professor at University of Warsaw