end-labeled DNA - translation to ρωσικά
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end-labeled DNA - translation to ρωσικά

WATER MADE OF UNCOMMON HYDROGEN AND OXYGEN ISOTOPES
Doubly-labeled water test; Doubly labeled water test; Doubly-labeled water

end-labeled DNA      

общая лексика

меченая по концам ДНК

DNA         
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  • date=22 September 2008 }}</ref>
  • 95px
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  • DNA major and minor grooves. The latter is a binding site for the [[Hoechst stain]] dye 33258.
  • animated version]]).
  • 3′]] hydroxyl group (—OH) on the other.
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  • lagging strand]]. This enzyme makes discontinuous segments (called [[Okazaki fragment]]s) before [[DNA ligase]] joins them together.
  • B]] and [[Z-DNA]]
  • language=en-US}}</ref>
  • Impure DNA extracted from an orange
  • Location of eukaryote [[nuclear DNA]] within the chromosomes
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  •  A current model of meiotic recombination, initiated by a double-strand break or gap, followed by pairing with an homologous chromosome and strand invasion to initiate the recombinational repair process. Repair of the gap can lead to crossover (CO) or non-crossover (NCO) of the flanking regions. CO recombination is thought to occur by the Double Holliday Junction (DHJ) model, illustrated on the right, above. NCO recombinants are thought to occur primarily by the Synthesis Dependent Strand Annealing (SDSA) model, illustrated on the left, above. Most recombination events appear to be the SDSA type.
  • Karyotype}}
  • language=en-US}}</ref>
  • [[Maclyn McCarty]] (left) shakes hands with [[Francis Crick]] and [[James Watson]], co-originators of the double-helix model based on the X-ray diffraction data and insights of Rosalind Franklin and Raymond Gosling.
  • Interaction of DNA (in orange) with [[histone]]s (in blue). These proteins' basic amino acids bind to the acidic phosphate groups on DNA.
  • website=ndbserver.rutgers.edu}}</ref>
  • Pencil sketch of the DNA double helix by Francis Crick in 1953
  • Simplified diagram
  • language=en-US}}</ref>
  • The Eagle]] [[pub]] commemorating Crick and Watson
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MOLECULE THAT ENCODES THE GENETIC INSTRUCTIONS USED IN THE DEVELOPMENT AND FUNCTIONING OF ALL KNOWN LIVING ORGANISMS AND MANY VIRUSES
Dna; History of science and technology/Discovery of DNA; Desoxyribonucleic acid; Naked DNA; SsDNA; Deoxyribonucleic Acid; Deoxiribose nucleic acid; DsDNA; Deoxyribose nucleic acid; Dsdna; Deoxyribionucleic acid; Deoxyribose Nucleic Acid; DNA gene; Dehydroxyribonucleic acid; DNA strand; Deoxyribonucleic Acids; Deoxyribonucleic acids; Deoxyribonucleic; DNA molecule; Doexyribonucleic acid; Deoxiribonewcleic; The blueprint of life; D.n.a.; Deroxiribonueclec acid; Deoxyribonucleic acid; Ssdna; Protein-DNA complex; SDNA; Dioxyribonucleic Acid; Double-stranded DNA; Dublex DNA; Single-stranded DNA; Sense and Antisense; Sense and antisense; Structure of DNA; Accessory genome; DNA world; Phosphodiester backbone; DNA helices; D. N. A.; 🧬; Sodium thymonucleate; History of DNA research; Extracellular DNA; DNA study; DNA studies; ABC acids

общая лексика

ДНК

дезоксирибонуклеиновая кислота

(Distributed Internet Application) распределённые приложения Интернет, архитектура DNA

(Digital Network Architecture) архитектура цифровой сети

сетевая архитектура, разработанная корпорацией Digital Equipment. Реализована в сети DECnet

синоним

deoxyribonucleic acid

Смотрите также

centromeric DNA; circular DNA; closed circular DNA; complementary DNA; cyclic DNA; denatured DNA; double-stranded DNA; end-labeled DNA; extrachromosomal DNA; foldback DNA; foreign DNA; genomic DNA; heteroduplex DNA; highly repetitive DNA; interspersed repeated DNA; junk DNA; linear DNA; linear duplex DNA; methylated DNA; mitochondrial DNA; naked DNA; native DNA; nick-translated DNA; noncoding DNA; nuclear DNA; nucleolar DNA; passenger DNA; plasmid DNA; recombinant DNA; renatured DNA; repetitive DNA; satellite DNA; selfish DNA; silent DNA; single-stranded DNA; spacer DNA; supercoiled DNA; template DNA; vector DNA; COM; DCOM; DAP

существительное

общая лексика

архитектура цифровых сетей

синоним

Digital Network Architecture

supercoil         
  • Supercoiled structure of circular DNA molecules with low writhe. The helical nature of the DNA duplex is omitted for clarity.
  • Figure showing the various conformational changes which are observed in circular DNA at different pH.  At a pH of about 12 (alkaline), there is a dip in the sedimentation coefficient, followed by a relentless increase up to a pH of about 13, at which pH the structure converts into the mysterious "Form IV".
  • Stochastic, prokaryotic model of the dynamics of RNA production and transcription locking at the promoter region, due to PSB.
  • Drawing showing the difference between a circular DNA chromosome (a plasmid) with a secondary helical twist only, and one containing an additional tertiary superhelical twist superimposed on the secondary helical winding.
  • Supercoiled structure of linear DNA molecules with constrained ends. The helical nature of the DNA duplex is omitted for clarity.
  • Illustration of how cold shock affects the supercoiling state of the DNA, by blocking the activity of Gyrase. The signs ‘ − ’ and ‘+’ represent negative and positive supercoiling, respectively. Created with BioRender.com. Also shown is a stochastic model of gene expression during cold shock as a function of the global DNA supercoiling state. The transition from ON to OFF of the promoter (P) causes the locking of transcription (i.e. RNA production). When ON, the promoter can produce RNA, from which proteins can be produced. RNA and proteins are always subject to degradation or dilution due to cell division.
COMPRESSED DNA LOOP SUPERCOILED BY PROKARYOTES TO FIT WITHIN A SMALL SPACE
Supercoil; Supercoiling; Dna, circular; Supercoiling of DNA; Positive supercoiling; Twist (DNA); Writhe (DNA); Supercoiled; Superhelical DNA energetics; Surface wrapping of DNA; DNA supercoiling; Circular genome; Supercoiled DNA; Superhelical DNA; Supertwisted DNA; Plectonemic supercoil; Linking number of DNA; Negative supercoiling; Superhelical dna

['s(j)u:pəkɔil]

общая лексика

суперспираль

спираль второго порядка

синоним

superhelix

Ορισμός

Эндоморфизм
(от Эндо... и греч. morphe - вид, форма)

отображение множества в себя, сохраняющее алгебраические операции и отношения, которые определены на этом множестве. Например, отображение х → 2х является Э. аддитивной группы целых чисел, так как 2(х + у) = 2x + 2y.

Βικιπαίδεια

Doubly labeled water

Doubly labeled water is water in which both the hydrogen and the oxygen have been partly or completely replaced (i.e. labeled) with an uncommon isotope of these elements for tracing purposes.

In practice, for both practical and safety reasons, almost all recent applications of the "doubly labeled water" method use water labeled with heavy but non-radioactive forms of each element (deuterium and oxygen-18). In theory, radioactive heavy isotopes of the elements could be used for such labeling; this was the case in many early applications of the method.

In particular, doubly labeled water (DLW) can be used for a method to measure the average daily metabolic rate of an organism over a period of time (often also called the Field metabolic rate, or FMR, in non-human animals). This is done by administering a dose of DLW, then measuring the elimination rates of deuterium and oxygen-18 in the subject over time (through regular sampling of heavy isotope concentrations in body water, by sampling saliva, urine, or blood). At least two samples are required: an initial sample (after the isotopes have reached equilibrium in the body), and a second sample some time later. The time between these samples depends on the size of the animal. In small animals, the period may be as short as 24 hours; in larger animals (such as adult humans), the period may be as long as 14 days.

The method was invented in the 1950s by Nathan Lifson and colleagues at the University of Minnesota. However, its use was restricted to small animals until the 1980s because of the high cost of the oxygen-18 isotope. Advances in mass spectrometry during the 1970s and early 1980s reduced the amount of isotope required, which made it feasible to apply the method to larger animals, including humans. The first application to humans was in 1982, by Dale Schoeller, over 25 years after the method was initially discovered. A complete summary of the technique is provided in a book by British biologist John Speakman.

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