were skewed towards the upper end of this range, giving an average value of 2.6 and standard deviation of 0.3 (45 samples). Selecting this average value as a starting point, SSA can be categorised as a material that is marginally less dense than the typical value of 2.65 for natural sand...
and except for the mass fraction of meteoritic iron (FeNi), and to a lesser degree phyllosilicates, specific heat is not very strongly dependent on the specific material. However, at low temperaturescPshows a strong temperature and compositional dependence. Specific heat must approach...
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The libraries were sequenced (paired-end, 150 cycles) on HiSeq-X (Illumina) machines with target coverages of 40× for the parental HMEC population, single-cell derived lineages (parental clones ae, bq, CQ and BF) and other derivative tetraploid clones (CQ-ev-B, CQ-ev-D, CQ-ev-H, ...
It can be defined by applying Legendre transformations to the first law of thermodynamics. The specific enthalpy of dielectric/electrocaloric material is defined as: (11)h=u−EP The derivative of this potential is: (12)ⅆh=ⅆu−PⅆE−EⅆP Inserting Eq. (4) into Eq. (12) it...
The same amount of material spread over a smaller area increases the WSG. From a physiological point of view, since the tree is taller, the water tension is much higher and the cell walls must therefore be thicker to withstand the pressure. Such effects may explain the steady increase in ...
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However, lectins must be identified from naturally occurring sources, whereas our aptamer selection platform allows the generation of entirely novel glycoprotein binders, with precise control over both the target and counter-target molecules. In some biological settings, lectins can achieve nanomolar ...
Approximately 30% of proteins that are newly synthesized in mammalian cells have a short half-life of less than 10 min, and must be rapidly degraded [25]. To achieve such high protein turnover rate, cells have evolved a specialized system for the selective and controlled unwanted protein ...
the enzyme must unbind the substrate entirely, and rebind it through a protein-protein interaction on the opposite Fc protomer in order to properly reposition its GH domain. The release of the Fc product (mono- or de-glycosylated) might be favored by destabilization of the C´ strand and ...