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Metkinen Universal Solid SupportThe universal support strategy offers the following clear advantages: eliminates the possibility of errors in parallel synthesis applications where up to 384 wells may contain different supports; eliminates the need for at least four supports for DNA synthesis and four for RNA synthesis; simplifies the preparation of oligonucleotides with modified or unusual nucleosides at the 3-terminus.Like our initial version of Universal Solid supports - USII, the new type of supports - Metkinen Universal Solid Support would be appropriate for the production of DNA oligos, long and short, as well as those requiring mild deprotection. It is compatible with the synthesis of RNA, (including siRNA) as well as virtually any oligonucleotide analogs (2-F-RNA, 2-OMe-RNA, LNA, oligonucleotide N3→P5 phosphoramidates, etc.). The reagent used for the cleavage/dephosphorylation step is commercially available and the procedures described are fully compatible with high-throughput Synthesis. The difference lies in the higher stability of Metkinen Universal Solid Support than that of USII upon prolong storage. In addition, the preparation of the new support appears to be more consistent and reliable. Metkinen Universal Solid Support is subject to proprietary rights of Glen Research Corporation and is synthesized and sold under the following licensed patents: US Patent No.: 6,770,754 and European Patent No.: 1404695. The new carbomoylation chemistry, resulting in the stable urea fragment, bridging the Universal linker and aminoalkylated solid phase, is subject to proprietary rights of Metkinen Chemistry (U.S. Patent Application Serial No. 60/854,721; International Patent Application No. PCT/ FI2007/050575).  Metkinen Universal Solid Support for synthesis of DNA, RNA & any type of modified oligonucleotides. Catalogue number: 103-00 Description: Chemically modified Macropourous Aminomethyl polystyrene. White to off-white powder. Storage of dry compound: 1 year at +20ēC Loading: 20-80 µmol/g g loadings is available. Please enquire for custom loading. Oligo synthesis on USIII: Perform oligonucleotide assembly, using standard protocols, recommended by your synthesizer manufacturer. Upon the completion of synthesis wash the oligonucleotide bound support with pure acetonitrile. Do not perform any washing steps with solvents, containing basic reagents (diethylamine, triethylamine, dimethylamine, etc.) and water! Cleavage: Cleave the oligo from the support using 3.5N - 4.5N ammonia in methanol (dilute cold 7N ammonia in methanol, Aldrich Cat. No 499145-100ML, with cold anhydrous methanol) at room temperature for 30 minutes. Do not use aqueous ammonium hydroxide and/or mixtures of ammonium hydroxide and methanol for cleavage! Deprotection AFTER Cleavage: Standard: After Cleavage, add 1 volume of 3.5N - 4.5N ammonia in methanol, seal and deprotect for 8-15 hours at 60 °C for removal of the protecting groups on the nucleobases. or Alternatively: add 1 volume of 30% ammonium hydroxide, seal and deprotect using the conditions appropriate for removal of the protecting groups on the nucleobases (e.g. at 55 °C for 5 hours). Price and Ordering Information |
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