نتایج جستجو برای: dna chromatography

تعداد نتایج: 607930  

2005
Keila Aparecida Moreira Margarida Diogo Duarte Miguel Prazeres José Luiz de Lima Filho Ana Lúcia Figueiredo Porto Manoel de Medeiros

This paper describes a method for the plasmid DNA purification, which includes an ammonium sulphate precipitation, followed by hydrophobic interaction chromatography (HIC) using Phenyl Sepharose 6 Fast Flow (low sub). The use of HIC took advantage of the more hydrophobic character of single stranded nucleic acid impurities as compared with double-stranded plasmid DNA.

Journal: :Chemical communications 2014
Wenbo Zhao Zhen Qin Chengsen Zhang Meiping Zhao Hai Luo

A label-free double amplification system has been developed by using a ternary DNA probe containing the poly(adenine-thymine) sequence assisted by exonuclease III degradation. The method achieved more than 600-fold signal amplification and allowed sensitive detection of single-stranded DNA and thrombin at the pM level by using liquid chromatography/mass spectrometry.

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1974
W G Baxt

DNA synthesized by particulate fractions from human leukemic white blood cells has been subfractionated by hybridization to Rauscher leukemia virus 70S RNA followed by hydroxylapatite chromatography. The Rauscher-leukemia-virus-specific DNA fraction is shown to be complementary only to sequences present in the nuclear DNA of Balb/c mouse spleens infected by this virus and the nuclear DNA from h...

Journal: :Acta medicinae Okayama 1969
M Omori

A series of experiments was conducted to study the base composition of DNA in AVl2-induced tumor and host cells by paper chromatography, and it was found that DNA per cent. guaninecystosine contents were around 42 % in both of them. The base composition of DNA of AV12 itself differs considerably from that of AVl2-induced tumor cells, while the DNA of tumor cells shows the property similar to th...

Journal: :Cancer research 1984
D Pruess-Schwartz S M Sebti P T Gilham W M Baird

A chromatographic procedure using boronic acid residues linked to a cellulose support [(N-(N'-[m-(dihydroxyboryl)-phenyl]succinamyl)amino]ethyl cellulose), used by Sawicki et al. (Cancer Res., 43: 3212-3218, 1983) for analysis of 7,12-dimethylbenz(a)anthracene:DNA adducts, was modified to allow the analysis of benzo(a)pyrene (BaP):DNA adducts formed in cells in culture. Adducts resulting from r...

شمسیان, بی بی شهین, حسینی گوهری, لادن , مستعان, لیلا , معینی علیشاه, فاطمه ,

Background & Aim: Since the mutant Hbs do not have any obvious electrical charge, globin chain separation is helpful for the diagnosis ofunknown Hbs. Therefore, the present study was carried out to detect alpha or beta chain variants by cation exchangechromatography.There are several point mutations in hemoglobin(Hb) genes which can cause hemoglobinopathy.Material and Method: count(CBC), HbA2 a...

Journal: :PLoS Biology 2004
David R Halpin Pehr B Harbury

Recently reported technologies for DNA-directed organic synthesis and for DNA computing rely on routing DNA populations through complex networks. The reduction of these ideas to practice has been limited by a lack of practical experimental tools. Here we describe a modular design for DNA routing genes, and routing machinery made from oligonucleotides and commercially available chromatography re...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1977
G A Galau R J Britten E H Davidson

The rate of reaction of double-stranded replicative form (RF) [3H]DNA of bacteriophage phiX174 with excess (+)strand DNA and (+)strand RNA was measured by standard methods of hydroxyapatite chromatography. The reactions follow pseudo-first-order kinetics and the observed rate constant for the RNA-DNA reaction differs less than 25% from that of the DNA-DNA reaction. The pseudo-first-order rate c...

Journal: :Journal of bacteriology 1973
J Sebastian M M Bhargava H O Halvorson

Two deoxyribonucleic acid (DNA)-dependent ribonucleic acid (RNA) polymerases (I, II) have been solubilized from isolated Saccharomyces cerevisiae nuclei. The enzymes can be separated by chromatography on O-diethylaminoethyl Sephadex. Both enzymes are active with high-molecular-weight nuclear yeast DNA, although RNA polymerase I has a higher affinity for polydeoxy-adenylic-thymidylic acid and RN...

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