Advanced Organic Chemistry of Nucleic AcidsWiley, 13 июл. 1994 г. - Всего страниц: 589 Z. Shabarova, A. Bogdanov Advanced Organic Chemistry of Nucleic Acids Sequencing, cloning, transcription -- these are but a few key techniques behind the current breathtaking advances in molecular biology and biochemistry. As these methods continuosly diversify, biochemists need a sound chemical understanding to keep the pace. Chemists beginning working in the molecular biology lab need an introduction to this field from their point of view. This book serves both: it describes most of the known chemical reactions of nucleosides, nucleotides, and nucleic acids in sufficient detail to provide the desired background, and additionally, the fundamental relations between sequence, structure and functionality of nucleic acids are presented. The first edition of this book, which was published in Russian, has immediately become a recognized standard reference. This second, thoroughly revised and updated edition, now published in English, is likely to achieve a similar position in the international scientific community. |
Содержание
Bonding Between Carbohydrate Moiety and Heterocyclic Base | 7 |
Nomenclature and Abridged Formulas of Nucleosides | 15 |
Pseudouridine | 23 |
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Другие издания - Просмотреть все
Advanced Organic Chemistry of Nucleic Acids Zoe A. Shabarova,Alexey A. Bogdanov Ограниченный просмотр - 2008 |
Advanced Organic Chemistry of Nucleic Acids Zoe A. Shabarova,Alexey A. Bogdanov Просмотр фрагмента - 1994 |
Advanced Organic Chemistry of Nucleic Acids Zoe A. Shabarova,Alexey A. Bogdanov Недоступно для просмотра - 2008 |
Часто встречающиеся слова и выражения
3'-terminal 5'-phosphate active acylation adenine adenosine alkaline alkyl amino group anhydrides aqueous solutions b.p. long base pairs carbohydrate moiety chemical cleavage cloning codons coli complementary complex compounds corresponding cytosine denaturation derivatives DNA fragments DNA ligase double helix double-stranded enzymatic enzyme ester example formation gene glycosidic glycosidic bond guanine guanosine helical heterocyclic heterocyclic bases HOCH2 hydrolysis hydroxyl interactions internucleotide linkages involved ligation method methyl modification molecular molecule monomer monomer units N-glycosidic bonds nitrogen nucleic acids nucleo nucleophilic substitution nucleotide nucleotide component nucleotide sequence OH OH oligo oligonucleotides oxidation pH values phate phosphate group phosphorus atom polymer polynucleotide polynucleotide chain presence primary structure protein proton purine purine bases pyrimidine reaction reactivity reagents residue result ribonucleoside ribose ribozyme RNase secondary structure segments single-stranded solid-phase stability stacking sticky ends strands synthesis synthetic tertiary structure tion triester tRNA uracil uridine vector yield он
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