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Amino Modifier

Amino Modifier

 

Amino modifiers play a critical role in oligonucleotide synthesis, allowing the attachment of various functional molecules such as dyes, biotin, and affinity tags through post-synthetic labeling. These modifications can be introduced at the 5′ or 3′ ends as well as internally, providing flexible customization options to enhance binding affinity, imaging capabilities, and targeted delivery. By extending the functionality of oligonucleotides, amino modifiers provide a reliable and cost-effective solution for a wide range of applications in research, diagnostics and therapeutics.

5' Modifications
Structure Change
Benefits

Amino(C3) , Amino(C6), Amino(C7)
Amino(C12)

Provides linkers of varying length for attaching different molecules

Reduces steric hindrance and improves conjugation efficiency, providing greater flexibility in labeling strategies

Abasic Amine

Introduces an amino group without a nucleobase

Minimizes interference with base pairing and is useful for applications requiring a neutral spacer

Amino6 (PEG1), Amino12(PEG3), Amino18(PEG5)

Incorporates polyethylene glycol (PEG) spacers

This modification can improve water solubility and reduce non-specific interactions

Internal Modifications
Structure Change
Benefits

Amino(C7)

Provides linkers of varying length for attaching different molecules

These internal modifications allow site-specific labeling within the oligo sequence and minimize disruption of the overall structure

Abasic Amine

Introduces an amino group without a nucleobase 

These internal modifications allow site-specific labeling within the oligo sequence and minimize disruption of the overall structure

Amino-C6-dA/dG/dC/dT

Introduces amino groups on specific nucleobases

Provides base-specific labeling options and versatility in designing complex probes

Amino-C2-dT, Aminoallyl-dT

Offers shorter linkers on thymine bases

This modification has minimal impact on duplex stability, and is useful for applications that require close proximity to the DNA backbone

3' Modifications
Structure Change
Benefits

Amino(C6), Amino(C7)

Provides linkers of varying length for attaching different molecules

This modification reduces steric hindrance and improves conjugation efficiency, providing greater flexibility in labeling strategies. It also protects against exonuclease degradation.

Abasic Amine

Introduces an amino group without a nucleobase

Minimizes interference with base pairing and is useful for applications requiring a neutral spacer. It also protects against exonuclease degradation.

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