Results 251 to 260 of about 299,739 (289)
ABSTRACT Molecular imprinting is a very powerful tool in life science. The research areas benefiting from a wide range of capabilities of molecularly imprinted polymeric nanoparticles (nanoMIPs) include sample preparation, extraction, sensing/detection, diagnostics, and drug delivery.
Milada Vodova+2 more
wiley +1 more source
Current Analytical Strategies for mRNA-Based Therapeutics. [PDF]
Camperi J+5 more
europepmc +1 more source
Navigating Uncertainties in RT-qPCR and Infectivity Assessment of Norovirus. [PDF]
Mirmahdi RS+3 more
europepmc +1 more source
The HBV variant CpF97L supports the secretion of pgRNA-containing virions at a level much greater than WT HBV. [PDF]
Kissi-Twum AA, Pionek K, Loeb DD.
europepmc +1 more source
Comprehensive nucleoside analysis of archaeal RNA modification profiles reveals an m<sup>7</sup>G in the conserved P loop of 23S rRNA. [PDF]
Tsai YL+10 more
europepmc +1 more source
pH-Reversible Cationic RNase A Conjugates for Enhanced Cellular Delivery and Tumor Cell Killing
Intracellularly-acting therapeutic proteins are considered promising alternatives for the treatment of various diseases. Major limitations of their application are low efficiency of intracellular delivery and possible reduction of protein activity during derivatization.
Xiaowen Liu+7 more
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RNase PH catalyzes a synthetic reaction, the addition of nucleotides to the 3′ end of RNA
Escherichia coli RNase PH is a phosphate-dependent exoribonuclease that has been implicated in the 3' processing of tRNA precursors. It degrades RNA chains in a phosphorolytic manner releasing nucleoside diphosphates as products. Here we show that RNase PH also catalyzes a synthetic reaction, the addition of nucleotides to the 3' termini of RNA ...
K A Ost, Murray P. Deutscher
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[68] Preparation of bacterial DNA by the phenol-pH 9-RNases method
Publisher Summary This chapter describes the method for the extraction of DNA from bacterial cells using phenol. Phenol treatment is considered one of the most effective methods for deproteinization. Whereas a neutral or acidic buffer (pH 5-7) extracts RNA into aqueous phase, rather than DNA from bacterial cells, in phenol treatment slightly alkaline
Kin‐ichiro Miura
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