Antisense Oligonucleotides
Multiple Options from R&D to Manufacturing Level
Home > Oligo Synthesis > Antisense Oligonucleotides
The General Introduction of Antisense Oligonucleotides
Synbio Technology offers antisense oligonucleotides (ASOs) that are specifically designed to target complementary RNA and prevent its translation into proteins. Our antisense oligos are ableto recognize specific mRNA sequences, thus blocking the translation of corresponding proteins, ultimately leading to the inhibition of gene expression.

Our synthesis process is optimized to produce high-quality antisense oligonucleotides that are engineered to provide maximum binding affinity and stability. By using state-of-the-art methods and cutting-edge technologies, such as HPLC purification and electrospray ionization mass spectrometry (ESI-MS), we ensure the highest levels of purity and accuracy. We are able to design and synthesize custom oligos for a variety of applications, including gene targeting, aptamer synthesis, and gene expression analysis.
Highlights
  • AI Design & Diverse Modifications
    Uses AI-optimized design with various modifications (e.g., MOE, 2'-F, 2'-O-Me)
  • Excellent Quality Stability
    Product purity >90%, batch-to-batch variation <0.01%
  • ISO 9001 and ISO 13485
    Certified quality control ensures reliability
  • Manufacturing Capability
    Microgram-to-gram-scale quantity
  • Delivery Speed
    Guaranteed fast delivery times without compromising quality
Service Details
Service Yield Purification Modifications Deliverables Turnaround Time
ASO Synthesis R & D level: ug-mg HPLC PTO, 2′-F, 2′-OME, 2′-MOE, LNA, Cholesterol, GalNAc, etc. ● Dry powder delivery, according to the customer needs of the separate packing.
● COA files.
1 Week
Manufacturing level: g HPLC PTO, 2′-F, 2′-OME, 2′-MOE, LNA, Cholesterol, GalNAc, etc. ● Dry powder delivery, according to the customer needs of the separate packing.
● COA files.
Inquire

* If you need other special modifications or pricing, please contact us for a quote at quote@synbio-tech.com.

Chemical Modification Common Name Class of Modification Activates RNase H1 Binding Affinity Effects Action
Phosphorothioate PS Backbone Yes Decreases Binds non-specifically to proteins, exists as two stereoisomers
2'-O-Methyl 2'-OMe Sugar No Increases Natural RNA modification; decreases toxicity
2'-O-Methoxyethyl 2'-MOE Sugar No Increases Reduces protein binding, decreased toxicity
Locked nucleic acids LNA Sugar No Increases High binding affinity at the cost of increased toxicity
5-Methylcytosine 5-MedC Base Yes Increases Natural RNA modification; prevents activation of TLR9 in CpG motifs
N-acetyl-galactosamine GalNAc Base No Decreases Targets hepatocytes via receptor-mediated endocytosis
2'-Fluoro  2'-F Sugar No Increases Increases stability of RNA by preventing hydrolysis
Cholesterol Cholesterol Base
(or non-nucleotide)
No Increases Improves cellular uptake and stability of oligonucleotides
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  • Address:
    9 Deer Park Dr., Suite J-25
    Monmouth Junction, NJ 08852

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