نتایج جستجو برای: oligonucleotide probes

تعداد نتایج: 67388  

Journal: :Nucleic Acids Research 2005
Johan Stenberg Fredrik Dahl Ulf Landegren Mats Nilsson

We describe PieceMaker, a software tool for the design of applications of selector probes-oligonucleotide probes that direct circularization of target nucleic acid molecules. Such probes can be combined in parallel to circularize a selection of fragments from restriction digested total genomic DNA. These fragments can then be amplified in a single PCR using a common primer pair, yielding substr...

Journal: :Nucleic acids research 1997
M S Shchepinov I A Udalova A J Bridgman E M Southern

Oligonucleotide dendrimers were synthesized using a novel phosphoramidite synthon, tris-2,2,2-[3-(4,4'-dimethoxytrityloxy) propyloxymethyl]ethyl- N , N -diisopropylaminocyanethoxy phosphoramidite. Label, incorporated using [gamma-32P]ATP and polynucleotide kinase, was increased in proportion to the number of 5'-ends. There was a similar increase in signal when these multiply labelled oligonucle...

Journal: :Nucleic acids research 1988
M S Urdea B D Warner J A Running M Stempien J Clyne T Horn

N4-[N-(6-trifluoroacetylamidocaproyl)-2-aminoethyl]-5'-O-dimethoxy trityl -5-methyl-2'-deoxycytidine-3'-N,N-diisopropyl-methylphosphoramidite++ + has been synthesized. This N4-alkylamino deoxycytidine derivative has been incorporated into oligonucleotide probes during chemical DNA synthesis. Subsequent to deprotection and purification, fluorescent (fluorescein, Texas Red and rhodamine), chemilu...

Journal: :Biosensors & bioelectronics 2007
Vivian C H Wu Sz-Hau Chen Chih-Sheng Lin

A DNA piezoelectric biosensing method for real-time detection of Escherichia coli O157:H7 in a circulating-flow system was developed in this study. Specific probes [a 30-mer oligonucleotide with or without additional 12 deoxythymidine 5'-monophosphate (12-dT)] for the detection of E. coli O157:H7 gene eaeA, synthetic oligonucleotide targets (30 and 104 mer) and PCR-amplified DNA fragments from ...

Journal: :Applied and environmental microbiology 1997
J Snaidr R Amann I Huber W Ludwig K H Schleifer

The bacterial community structure of activated sludge of a large municipal wastewater treatment plant was investigated by use of the rRNA approach. Almost-full-length genes coding for the small-subunit rRNA (rDNA) were amplified by PCR and subsequently cloned into the pGEM-T vector. Clones were screened by dot blot hybridization with group-specific oligonucleotide probes. The phylogenetic affil...

Journal: :BioTechniques 1998
S G Daniel M E Westling M S Moss B D Kanagy

The FastTag Nucleic Acid Labeling System couples haptens, fluorochromes or affinity ligands to any nucleic acid by attaching a universal, photo-or heat-activatable moiety to which any sulfhydryl-reactive compound can be linked. To demonstrate the versatility of the FastTag system, we have labeled DNA, RNA and oligonucleotide probes with a variety of maleimide-coupled moieties and have used thes...

Journal: :Biochemistry 1994
W M Olivas L J Maher

Duplex DNA recognition by oligonucleotide-directed triple helix formation is generally limited to homopurine target domains. Various approaches have been suggested for the relief of this constraint. Artificial DNA sequences have previously been used to show that adjacent homopurine domains on opposite DNA strands can be simultaneously recognized by oligonucleotide probes that switch triple heli...

Journal: :Applied and environmental microbiology 2012
Faris Behnam Andreas Vilcinskas Michael Wagner Kilian Stoecker

Fluorescence in situ hybridization (FISH) with rRNA-targeted oligonucleotide probes is an essential tool for the cultivation-independent identification of microbes within environmental and clinical samples. However, one of the major constraints of conventional FISH is the very limited number of different target organisms that can be detected simultaneously with standard epifluorescence or confo...

2003
Tadashi Kadowaki Satoshi Shiojima Gozoh Tsujimoto

Alternative splicing is the phenomena that the pre-mRNA transcript from DNA is processed into different mRNAs by spliced different types of introns. The organism can acquire proteins as many times as genes. Therefore to find such splicing variants is risen in the post genome era. We investigate a new method to detect splicing variants with the gene expression data by the oligonucleotide array t...

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