نتایج جستجو برای: plasmid relaxation assay

تعداد نتایج: 330063  

Journal: :The Analyst 2011
Shaoyu Cai Guohai Liang Peng Zhang Hui Chen Song Zhang Baohong Liu Jilie Kong

A rational strategy of magnetic relaxation switches was proposed here to detect a(1)-acid glycoprotein (AGP), an acute phase a-globulin plasma glycoprotein. The assay was based on the relaxation time change between the aggregation of magnetic nanoparticles with concanavalin A and the redispersion with AGP, which can avoid the prozone effect and improve the detection accuracy. The assay was an e...

Journal: :American journal of physiology. Heart and circulatory physiology 2007
Mahmoud Saifeddine Michelle L Seymour Yu-Pei Xiao Steven J Compton Steeve Houle Rithwik Ramachandran Wallace K MacNaughton Serge Simonet Christine Vayssettes-Courchay Tony J Verbeuren Morley D Hollenberg

In canine coronary artery preparations, the proteinase-activated receptor-2 (PAR(2)) activating peptides (PAR(2)-APs) SLIGRL-NH(2) and 2-furoyl-LIGRLO-NH(2) caused both an endothelium-dependent relaxation and an endothelium-independent contraction. Relaxation was caused at peptide concentrations 10-fold lower than those causing a contractile response. Although trans-cinnamoyl-LIGRLO-NH(2), like...

2010
Vanessa A. Marrero Lorraine S. Symington

Homology-dependent repair of DNA double-strand breaks (DSBs) by gene conversion involves short tracts of DNA synthesis and limited loss of heterozygosity (LOH). For DSBs that present only one end, repair occurs by invasion into a homologous sequence followed by replication to the end of the chromosome resulting in extensive LOH, a process called break-induced replication (BIR). We developed a B...

Journal: :Molecular cancer therapeutics 2015
Yeonee Seol Hongliang Zhang Keli Agama Nicholas Lorence Yves Pommier Keir C Neuman

Human nuclear type IB topoisomerase (Top1) inhibitors are widely used and powerful anticancer agents. In this study, we introduce and validate a single-molecule supercoil relaxation assay as a molecular pharmacology tool for characterizing therapeutically relevant Top1 inhibitors. Using this assay, we determined the effects on Top1 supercoil relaxation activity of four Top1 inhibitors; three cl...

Journal: :Carcinogenesis 1997
M N Routledge J M Allan R C Garner

To investigate the use of UvrB-binding to detect DNA damage, mobility shift gel electrophoresis was used to detect binding of UvrB protein to a 136 bp DNA fragment that was randomly adducted with aflatoxin B1 8,9-epoxide and end-labelled with 32P. After polyacrylamide gel electrophoresis, the shifted band that contained DNA bound by UvrB was quantified as a percentage of total radioactive subst...

Journal: :Journal of clinical microbiology 1992
A R Wanger S L Morris C Ericsson K V Singh M T LaRocco

An unusual strain of methicillin-resistant Staphylococcus aureus (MRSA) was repeatedly isolated from infants in a newborn special care unit (NBSC) and a newborn intensive care unit. Between January 1989 and March 1990, approximately 100 isolates from infected or colonized infants were recovered. Surveillance cultures taken during this time revealed a 20% colonization rate, which was defined as ...

Journal: :Investigative ophthalmology & visual science 2004
Nancy C Joyce Deshea L Harris James C Mc Alister Robin R Ali Daniel F P Larkin

PURPOSE To test the hypothesis that overexpression of the transcription factor E2F2 promotes cell cycle progression in nonproliferating corneal endothelial cells. METHODS Ex vivo rabbit corneas were transfected with a lipid transfection reagent and either a control plasmid containing full-length cDNA for enhanced green fluorescent protein (pIRES2-EGFP) or a plasmid containing full-length cDNA...

2016
Jorge Aguiar Gerardo García Yamila León Eduardo Canales José Angel Silva Omar Gell Regla Estrada Ivis Morán Verena Muzio Gerardo Guillén Eduardo Pentón Julio Cesar Aguilar

Aim We studied the functional stability of a primer pair and the standard curve based on a plasmid carrying full-length HBV genome, from a novel low-cost real-time quantitative polymerase chain reaction (qPCR) assay. The assay was developed at the Center for Genetic Engineering and Biotechnology (CIGB) in Havana, to quantify the serum hepatitis B virus (HBV) DNA from chronic HBV-infected (CHB) ...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید