25 research outputs found
Process reduces secondary resonant emission in electronic components
Process reduces secondary electron emission in coaxial connector and in waveguides in the atmosphere. The assembly is placed in a vacuum chamber and is gradually vented to the atmosphere. It is exposed to high voltage, argon gas, and a hydrocarbon gas during the process
Process for reducing secondary electron emission Patent
Method for treating metal surfaces to prevent secondary electron transmissio
Improved vacuum deposition apparatus
Improved apparatus enables vacuum deposition of thick metal films on the inside surface of a cylinder. The evaporant is deposited to a uniform thickness and distribution on the inside surface of the substrate without imperfections that would otherwise result from droplet formation
Means and methods of depositing thin films on substrates Patent
Means and methods of depositing thin films on substrate
Method of producing a storage bulb for an atomic hydrogen maser
A storage bulb for an atomic hydrogen maser is produced by coating its internal surface with an emulsion containing both TFE and FEP particles. The emulsion is produced by mixing a first quantity of TFE in an aqueous dispersion with a second quantity of FEP in an aqueous dispersion, with a third quantity of distilled water. The emulsion is poured into the bulb to coat it uniformly so as to form a thin film of emulsion on the bulb's internal surface. After excess emulsion is drained out of the bulb the emulsion in the bulb is dried to remove the water and most of the aqueous matter therefrom. The remaining emulsion is then cured by heating the bulb to a temperature of at least 380 C
Antiviral responses of human Leydig cells to mumps virus infection or poly I:C stimulation
International audienceBACKGROUND: The immuno-privileged status of the testis is essential to the maintenance of its functions, and innate immunity is likely to play a key role in limiting harmful viral infections, as demonstrated in the rat. In men mumps virus infects Leydig cells and has deleterious effects on testosterone production and spermatogenesis. The aim of this study was to test whether mumps virus infection of isolated human Leydig cells was associated with an inhibition of their innate antiviral defences. METHODS: Leydig cell production of mRNA and protein for interferons (IFNs) and of three antiviral proteins-2'5' oligoadenylate synthetase (2'5'OAS), double-stranded RNA-activated protein kinase (PKR) and MxA-was investigated, in the absence or presence of mumps virus or viral stimuli including poly I:C, a mimetic of RNA viruses replication product. RESULTS: Stimulated or not, human Leydig cells appeared unable to produce routinely detectable IFNs alpha, beta and gamma. Although the level of PKR remained unchanged after stimulation, the expression of 2'5'OAS and MxA was enhanced following either mumps virus or poly I:C exposure (P < 0.05 versus control). CONCLUSIONS: Overall, our results demonstrate that mumps virus replication in human Leydig cells is not associated with a specific inhibition of IFNs or 2'5'OAS, MxA and PKR production and that these cells display relatively weak endogenous antiviral abilities, as opposed to their rat counterparts