نتایج جستجو برای: dna chromatography

تعداد نتایج: 607930  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1975
J G Chirikjian L Rye T S Papas

Pyran covalently linked to cyanogen bromide-activated Sepharose has been shown to be an effective affinity matrix for several viral DNA polymerases. Differential salt elution of viral compared with cellular polymerases, as well as substrate elution, suggests the affinity nature for the matrix. Unlike some other affinity systems described, pyran-Sepharose is totally resistant to nuclease digesti...

Journal: :BioTechniques 2007
Herbert Oberacher Walther Parson

The determination of the molecular mass of a DNA sequence has several benefits over conventional fragment-length analysis that are advantageous to the forensic field: (i) sequence variation is captured that increases the power of discrimination compared with that obtained by conventional fragment-length analysis. First experiments showed that this increase makes up to 20%-30% for STR analysis. ...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1975
J Rouvière-Yaniv F Gros

A low-molecular-weight (7000), heat-stable protein--HU--that stimulates transcription of bacteriophage lambda DNA by E. coli RNA polymerase was purified from E. coli extracts using affinity chromatography on DNA-cellulose. HU binds to native DNA, resulting in an apparent thickening of the DNA chains as revealed by electron microscopy. Contrary to DNA unwinding proteins, it causes no destabiliza...

Journal: :Acta biochimica Polonica 2002
Yuri Kit Elena Kuligina Dimitry Semenov Vladimir Richter

Preparations of anti-DNA sIgA were obtained from human milk by sequential chromatography on protein A-sepharose, DEAE-fractogel and DNA-cellulose. The influence of oligonucleotides on protein kinase activity was investigated. It was discovered that incubation of anti-DNA sIgA with oligodeoxyriboadenylate d(A)12 stimulates the phosphorylation of polypeptides of sIgA in the presence of [gamma-32P...

Journal: :Molecular & cellular proteomics : MCP 2016
Jacob J Kennedy Ping Yan Lei Zhao Richard G Ivey Uliana J Voytovich Heather D Moore Chenwei Lin Era L Pogosova-Agadjanyan Derek L Stirewalt Kerryn W Reding Jeffrey R Whiteaker Amanda G Paulovich

A major goal in cell signaling research is the quantification of phosphorylation pharmacodynamics following perturbations. Traditional methods of studying cellular phospho-signaling measure one analyte at a time with poor standardization, rendering them inadequate for interrogating network biology and contributing to the irreproducibility of preclinical research. In this study, we test the feas...

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