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Therefore, this 100-K limit seems adequate for these molecules in general.
Intrabodies (IB) are suitable tools to down-regulate the expression of cell surface molecules in general.
To date, it is just known only that SMMs and other large molecules in general may decompose over time [35].
In order to capture the evolutionary advantage of NPs, it is of high relevance to develop methods for their differentiation from chemical molecules in general, separating NPs and NP-like compounds out of the set of all chemical structures.
To advance both the study of circular polarization in pho-tosynthetic pigments as well as circular polarization of ho-mochiral molecules in general, we also performed a computational survey of the effect that properties of aggregates, used to simulate biological objects, have on circular polarization.
However, it was shown that a great quantity of oligomers (cyclic products) is produced from propene at low temperatures on MCM-41-type catalysts and that the pore size of the mesoporous material can make a difference when the aim is to oligomerise larger olefins or to produce large lubricant molecules in general [12].
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The economics underlying derivative products are so novel and significant that four of their innovators have won Nobel prizes".Derivative product" is to "molecule" in general as each of Mr Drucker's favourite financial products (for example, Eurodollars, Eurobonds and credit cards) is to a specific molecule.
The precise frequency at which a particular chromophore absorbs depends significantly on the other constituents of the molecule, in general the frequency range over which its absorption is found will not be as narrow as the range of the infrared vibrational frequency associated with a specific structural entity.
The loading and stimuli-responsive release of transition metals and any drug molecule in general from a delivery are major factors that ultimately determine the success or failure of that vector when applied to targeted drug delivery.
The electron density for the dimethylamino-ethylamide moiety of 6 was weak in relation to the aromatic part, most likely due to increased flexibility of this part of the molecule in general, and specifically this moiety extended outwards from the binding pocket and did not interact with DAPK1.
The biodistribution of all 188Re-labeled affibody molecules was in general comparable, with the main observed difference found in the uptake and retention of radioactivity in excretory organs.
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