نتایج جستجو برای: dna release

تعداد نتایج: 711962  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2000
O Lambert L Letellier W M Gelbart J L Rigaud

We report a strategy for encapsulating and condensing DNA. When T5 phage binds to its membrane protein receptor, FhuA, its double stranded DNA (120,000 bp) is progressively released base pair after base pair in the surrounding medium. Using cryoelectron microscopy, we have visualized the structures formed after T5 phage DNA is released into neutral unilamellar proteoliposomes reconstituted with...

Journal: :Journal of clinical microbiology 1997
J Löffler H Hebart U Schumacher H Reitze H Einsele

Five commercially available extraction kits and an in-house DNA extraction method for the release of DNA from Candida albicans and Aspergillus niger cells were assessed for sensitivity, purity, duration, and cost. All commercially available kits helped to shorten the duration of DNA extraction. However, the sensitivity varied from 1 to 1,000 fungal cells/ml and costs varied from $0.10 to 2.30. ...

Journal: :Bioconjugate chemistry 2005
Gang Han Nandini S Chari Ayush Verma Rui Hong Craig T Martin Vincent M Rotello

Positively charged trimethylammonium-functionalized mixed monolayer protected clusters (MMPCs) bind DNA through complementary electrostatic interactions, resulting in complete inhibition of DNA transcription of T7 RNA polymerase. DNA was released from the nanoparticle by intracellular concentrations of glutathione, resulting in efficient transcription. The restoration of RNA production was dose...

2006
U. Lonn S. Lonn

DNA synthesis was investigated in human malignant mela noma cells. The DNA was extracted in a neutral nondenaturing buffer at 25°and characterized by agarose gel electrophoresis. Radioactive DNA pulse labeled for 10 to 30 min was released from the chromosomes in the form of double-stranded frag ments. The release of the fragments from the chromosomes is prevented by lysing the cells at 0°inst...

2015
Kata Sarlós Máté Gyimesi Zoltán Kele Mihály Kovács

The processing of various DNA structures by RecQ helicases is crucial for genome maintenance in both bacteria and eukaryotes. RecQ helicases perform active destabilization of DNA duplexes, based on tight coupling of their ATPase activity to moderately processive translocation along DNA strands. Here, we determined the ATPase kinetic mechanism of E. coli RecQ helicase to reveal how mechanoenzyma...

Journal: :Proceedings of the National Academy of Sciences 1973

Journal: :Proceedings of the National Academy of Sciences 1970

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