نتایج جستجو برای: complementary dna

تعداد نتایج: 577711  

Journal: :The Journal of Cell Biology 1980
J F Catterall J P Stein P Kristo A R Means B W O'Malley

Ovomucoid messenger RNA (mRNAom) comprises approximately 8% of the total mRNA in the estrogen-stimulated oviduct. The recombinant plasmid pOM100 contained DNA complementary to the 3' end of mRNAom. DNA complementary to the 5' end of mRNAom was obtained from a partially purified preparation of mRNAom by polymerization by reverse transcriptase in the presence of a restriction fragment primer from...

2011
Damian Ittig Anna-Barbara Gerber Christian J. Leumann

A series of oligodeoxyribonucleotides and oligoribonucleotides containing single and multiple tricyclo(tc)-nucleosides in various arrangements were prepared and the thermal and thermodynamic transition profiles of duplexes with complementary DNA and RNA evaluated. Tc-residues aligned in a non-continuous fashion in an RNA strand significantly decrease affinity to complementary RNA and DNA, mostl...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2009
Robert J Macfarlane Byeongdu Lee Haley D Hill Andrew J Senesi Soenke Seifert Chad A Mirkin

We present an analysis of the key steps involved in the DNA-directed assembly of nanoparticles into crystallites and polycrystalline aggregates. Additionally, the rate of crystal growth as a function of increased DNA linker length, solution temperature, and self-complementary versus non-self-complementary DNA linker strands (1- versus 2-component systems) has been studied. The data show that th...

2013
Oya Bermek Nigel D. F. Grindley Catherine M. Joyce

The accuracy of high-fidelity DNA polymerases such as DNA polymerase I (Klenow fragment) is governed by conformational changes early in the reaction pathway that serve as fidelity checkpoints, identifying inappropriate template-nucleotide pairings. The fingers-closing transition (detected by a fluorescence resonance energy transfer-based assay) is the unique outcome of binding a correct incomin...

Journal: :Journal of Analytical Science and Technology 2021

Abstract Background In this paper, a simple, enzyme-free, label-free fluorescence, high sensitivity logic gate hairpin aptasensor was developed for adenosine triphosphate (ATP) detection based on graphene oxide (GO) and PicoGreen dye. Methods Using single-strand deoxyribonucleic acid (DNA) as input signal fluorescence output signal, if DNA (DNA-L), (DNA-S), ATP were present at the same time, on...

Journal: :Nucleic acids research 1991
K Saunders A Lucy J Stanley

We have analysed DNA from African cassava mosaic virus (ACMV)-infected Nicotiana benthamiana by two-dimensional agarose gel electrophoresis and detected ACMV-specific DNAs by blot-hybridisation. ACMV DNA forms including the previously characterised single-stranded, open-circular, linear and supercoiled DNAs along with five previously uncharacterised heterogeneous DNAs (H1-H5) were resolved. The...

2010
Sebastian Sorgenfrei Chien-yang Chiu Ruben L. Gonzalez Young-Jun Yu Philip Kim Colin Nuckolls Kenneth L. Shepard

1. Fabrication of devices 2. Lifetime histograms with probe DNA NH2-5’-GGAAAAAAGG-3’ (Device 1) 3. Measurements with probe DNA NH2-5’-GTGAGTTGTT-3’ (Device 2) 4. Lifetime histograms with probe DNA NH2-5’-GTGAGTTGTT-3’ (Device 2) 5. Control experiment with a non-functionalized device 6. Scanning gate microscopy (IV) 7. Control experiments with probe DNA NH2-5’-GGAAAAAAGG-3’ with complementary an...

2003
Paul Gauthier Michael Ringenburg

DNA microarrays are a powerful technology for analysis of gene expression levels within cells. Both the cDNA and oligonucleotide technologies for microarrays are fairly young and are prone to a broad collection of errors and inaccuracies [KYML02]. In this paper we briefly discuss some sources of error and detail a variety of methods for normalizing the data with respect to some of these error s...

Journal: :Nucleic acids research 1979
G. R. Stark J. G. Williams

Substantial amounts of DNA (at least 25 microgram per cm2) can be stably bound to diazobenzyloxymethyl (DBM)-paper. Complementary RNA will hybridize to the DNA paper almost completely in 24 hours. Using several different conditions of hybridization and washing, the background of RNA bound non-specifically is very low (between 0.01 and 0.02%) and the efficiency of hybridization is very high (75 ...

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