Building on from the existing range of standard nucleobase RNA phosphoramidites and CPG supports, the modified RNA-type phosphoramidites comprise two new 2’-OMe RNA products, 2’-OMe-I and 2’-OMe-T. Oligonucleotides containing these modifications are ideal for triplex, antisense and gene targeting studies, as they form more stable hybrids with complementary RNA strands compared to equivalent DNA or RNA strands. Furthermore, when used in gene targeting studies, the addition of 2’-OMe residues into triplex forming oligonucleotides (TFO’s), confers the same nuclease resistance and stability as seen with duplexes.
Oligonucleotides synthesised from Link’s new ethyl phosphoramidites (available with standard nucleobase protection) have a neutral charge and slightly lipophilic character, which improves their delivery into the cell. Perfect for use in therapeutic applications, oligonucleotides containing these ethyl groups are nuclease resistant and have been shown to inhibit protein expression and cell growth when taken up by liposomes.
Dr Catherine McKeen, Technical Manager at Link Technologies, commented: “We understand the importance of evolving our product offering to reflect the developing needs of our customers. As part of this, the new modified phosphoramidites provide increased nuclease resistance and stability, extending the experimental capabilities available to our customers.”
For more information please visit the Link Technologies website at www.linktech.co.uk or follow us on Twitter: @linktechdna. You can also find out more about Link’s recent product updates by reading the company’s latest blog post.