Also found in: Medical.
NS3Netscape 3
NS3Non-Structural 3 Protein (immunology)
NS3Network Survivability - Triple Link Failure
NS3NASA (National Aeronautics and Space Administration) Supercomputing Support Services (US NASA)
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References in periodicals archive ?
aegypti for their ability to drive high constitutive expression of exogenous proteins (GFP and NS3 proteins of two flaviviruses) in the mosquito cell lines C6/36 and CCL125, Drosophila S2 cells, and Spodoptera frugiperda (moth) Sf21 cells.
Analysis of the site suggested that it will hinder the interactions of NS3 with its cofactor NS2B, leading the inhibition of protease as reported by Shiryaev et al.
In this study, the plasmid DNAs encoding Hsp20, NS3, Hsp20-NS3 were generated and their expression was evaluated in mammalian cell line using a cationic polymer (TurboFect) and a cationic lipid (Lipofectamine).
From these NS proteins, we know the function of NS3 the most.
The anti-HCV protease activity was carried out for the crude extracts of the isolated endophytic fungal strains in 100 ug/ml concentration using the hepatitis virus C NS3 protease inhibitor 2 as a positive control.
In addition to exhibiting these popular offerings at NS3, Visionet will be showcasing its new Robotic Process Automation (RPA) services.
The monoantibody (mAb) to HCV Core (ab2740) or NS3 (ab13830) was from Abcam, Co.
The extracted RNA was transcribed to cDNA and the NS3, NS5A, and NS5B fragments were amplified by polymerase chain reaction (PCR) in a one-step process (Superscript III One-step RT-PCR with platinum Taq kit; Invitrogen, Carlsbad, CA, USA) following the manufacturers' instructions.
The use of NovelSat NS3 technology on the AFRICASAT-1a satellite enabled an increase in spectral efficiency levels by between 20% and 50%.
Jacobson, "The first wave: HCV NS3 protease inhibitors telaprevir and boceprevir," Antiviral Therapy, vol.
Phosphoprotein NS5A, although typically not considered to display direct enzymatic activity, constitutes an essential component of the HCV replicase and it has also been shown to "cross-talk" with most non-structural proteins (e.g., NS2, NS3, NS4A, NS4B, etc).
R155 is the main overlapping position for drug resistance, and different mutations at this site within the NS3 protease confer resistance to nearly all protease inhibitors.