نتایج جستجو برای: rna purification

تعداد نتایج: 304817  

Journal: :Biophysical chemistry 2016
V Vaghi C Potrich L Pasquardini L Lunelli L Vanzetti E Ebranati A Lai G Zehender D Mombello M Cocuzza C F Pirri C Pederzolli

Hepatitis C virus (HCV) is one of the main causes of chronic liver disease worldwide. The diagnosis and monitoring of HCV infection is a crucial need in the clinical management. The conventional diagnostic technologies are challenged when trying to address molecular diagnostics, especially because they require a complex and time-consuming sample preparation phase. Here, a new concept based on s...

Journal: :Methods in molecular biology 2015
Arlie J Rinaldi Krishna C Suddala Nils G Walter

The recent discovery that non-coding RNAs are considerably more abundant and serve a much wider range of critical cellular functions than recognized over previous decades of research into molecular biology has sparked a renewed interest in the study of structure-function relationships of RNA. To perform their functions in the cell, RNAs must dominantly adopt their native conformations, avoiding...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1986
Z A Khan K T Hiriyanna F Chavez H Fraenkel-Conrat

Much work has been done on the isolation, purification, and characterization of the RNA-directed RNA polymerase (EC 2.7.7.48) of cucumber mosaic virus (CMV)-infected cucumbers. Uninfected plants were reported to have no such enzyme, but we recently detected low levels of the activity in cucumber. Since tobacco and cowpea contain such an enzyme that is variably increased in amount by various vir...

2015
Siqi Tian Joseph D. Yesselman Pablo Cordero Rhiju Das

Customized RNA synthesis is in demand for biological and biotechnological research. While chemical synthesis and gel or chromatographic purification of RNA is costly and difficult for sequences longer than tens of nucleotides, a pipeline of primer assembly of DNA templates, in vitro transcription by T7 RNA polymerase and kit-based purification provides a cost-effective and fast alternative for ...

2015
Sarah Temmam Sonia Monteil-Bouchard Catherine Robert Hervé Pascalis Caroline Michelle Priscilla Jardot Rémi Charrel Didier Raoult Christelle Desnues Patrick Tang

BACKGROUND Metagenomic analyses have been widely used in the last decade to describe viral communities in various environments or to identify the etiology of human, animal, and plant pathologies. Here, we present a simple and standardized protocol that allows for the purification and sequencing of RNA viromes from complex biological samples with an important reduction of host DNA and RNA contam...

Journal: :Nucleic acids research 1992
C Hernández J A Daròs S F Elena A Moya R Flores

The sequence of a circular RNA from carnation has been determined and found to consist of 275 nucleotide residues adopting a branched secondary structure of minimum free energy. Both plus and minus strands of this RNA can form the hammerhead structures proposed to mediate the in vitro self-cleavage of a number of small infectious plant RNAs and the transcript of satellite 2 DNA from the newt. M...

2018
Giorgio Giurato Giovanni Nassa Annamaria Salvati Elena Alexandrova Francesca Rizzo Tuula A Nyman Alessandro Weisz Roberta Tarallo

The nuclear receptor estrogen receptor 2 (ESR2, ERβ) modulates cancer cell proliferation and tumor growth, exerting an oncosuppressive role in breast cancer (BC). Interaction proteomics by tandem affinity purification coupled to mass spectrometry was previously applied in BC cells to identify proteins acting in concert with ERβ to control key cellular functions, including gene transcription, RN...

Journal: :BioTechniques 2002
Qing S Wang Peter J Unrau

Here we report the construction of a histidine-tagged T4 RNA ligase expression plasmid (pRHT4). The construct, when overexpressed in BL21 (DE3) cells, allows the preparation of large quantities of T4 RNA ligase in high purity using only a single purification column. The histidine affinity tag does not inhibit enzyme function, and we were able to purify 1-3 mg pure protein/g cell pellet. A simpl...

2003

Here we report the construction of a histidine-tagged T4 RNA ligase expression plasmid (pRHT4). The construct, when overexpressed in BL21 (DE3) cells, allows the preparation of large quantities of T4 RNA ligase in high purity using only a single purification column. The histidine affinity tag does not inhibit enzyme function, and we were able to purify 1–3 mg pure protein/g cell pellet. A simpl...

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