We've updated our Privacy Policy to make it clearer how we use your personal data.

We use cookies to provide you with a better experience. You can read our Cookie Policy here.


IDT Offers Oligonucleotides to Suit all Applications

Want a FREE PDF version of This Product News?

Complete the form below and we will email you a PDF version of "IDT Offers Oligonucleotides to Suit all Applications"

Technology Networks Ltd. needs the contact information you provide to us to contact you about our products and services. You may unsubscribe from these communications at any time. For information on how to unsubscribe, as well as our privacy practices and commitment to protecting your privacy, check out our Privacy Policy

Integrated DNA Technologies (IDT), offers a comprehensive oligo manufacturing service with rapid turnaround times. All oligos are provided deprotected, desalted, quantified using UV spectrophotometry and checked for quality using mass spectrometry as standard, to provide the highest quality and yield accuracy currently available.

Oligos are available in a range of amounts, from 25 nmol up to 10 µmol with the additional option of large-scale production up to 10 g. As well as providing standard length oligos, IDT’s chemistry expertise allows the production of high quality, long Ultramer DNA oligos,up to 200bp in length, making them ideal for gene construction, cloning, and DNA-directed RNA interference (ddRNAi).

Oligos can be delivered in individual tubes, as well as 96 or 384 well plates, either lyophilized or resuspended in liquid, such as water or Tris-EDTA (TE) buffer. For high-throughput laboratories, IDT offers a HOTplate service, shipping larger batches of unmodified DNA oligos with next day delivery. For smaller scale use, individual unmodified DNA oligos between 15 and 45bp in length can be shipped using IDT’s SameDay high speed delivery service.

Custom RNA oligoscan be synthesized and shipped with a fast turnaround of 2-3 business days. Where a higher degree of oligo purity is required, oligos can be purified using PAGE or HPLC. In addition, it is possible to include user-specified modifications such as nucleotide phosphorylation, fluorophore incorporation or the use of modified bases (e.g. 5-Bromo-deoxyuridine).