Abstract:
:Synthetic deoxyoligonucleotides have been 5'-aminoalkylated at the end of step-wise synthesis on the polymer support. This was achieved through the activation of the 5'-hydroxyl group as its 5'-imidazolyl derivative using carbonyldiimidazole, which was subsequently displaced with hexamethylene diamine to yield the title compound. The alkyl carbamate linkage thus generated withstands the deprotection conditions used in oligonucleotide synthesis. Purification by gel electrophoresis and further derivatization at the 5'-amino group with N-hydroxysuccinimidobiotin is described.
journal_name
Nucleic Acids Resjournal_title
Nucleic acids researchauthors
Wachter L,Jablonski JA,Ramachandran KLdoi
10.1093/nar/14.20.7985subject
Has Abstractpub_date
1986-10-24 00:00:00pages
7985-94issue
20eissn
0305-1048issn
1362-4962journal_volume
14pub_type
杂志文章abstract::The European Nucleotide Archive (ENA; http://www.ebi.ac.uk/ena) is Europe's primary resource for nucleotide sequence information. With the growing volume and diversity of public sequencing data comes the need for increased sophistication in data organisation, presentation and search services so as to maximise its disc...
journal_title:Nucleic acids research
pub_type: 杂志文章
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doi:10.1093/nar/21.24.5720
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pub_type: 杂志文章
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journal_title:Nucleic acids research
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journal_title:Nucleic acids research
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journal_title:Nucleic acids research
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