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Modern methods for the synthesis and purification of these molecules will also be presented.
The applicability of these titanosilicates to catalytic oxidation processes requiring bulky organic molecules will also be presented.
In this chapter, important interferences of heterophilic antibodies with various immunoassays (especially immunoassays) used for analysis of large molecules will also be addressed.
The identification of arrestin-binding sites for various signaling molecules will also set the stage for designing molecular tools for therapeutic intervention that may prove useful in numerous disorders associated with congenital or acquired disregulation of GPCR signaling.
Furthermore, alizarin and purpurin dye molecules will also form aggregates by the dye-metal-dye chelation (Ahn et al., 2014).
This observation suggests that transcripts corresponding to potential novel taste receptors, receptor-associated proteins, and signal transduction molecules will also be enriched in the top fraction of taste buds.
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At the same time, the surface charge of IgG molecule will also contribute to the increase of the total ionic current when it passes through nanopore.
If a query molecule is a substructure of a target molecule, then all of the bits set in the query molecule will also be set in the target molecule.
(2) Surface charge density of IgG molecule: as we know, the surface charge of IgG molecule will also contribute to the increase of total ionic current when it passes through the nanopore.
Secondly, the presence of chloro- group, an electron withdrawing group, in the 4-CP molecule will also reduce the electron density of aromatic ring which consequentially beefed up the interaction of phenol ring and SAC (Deng et al. 1997).
Furthermore, these findings reveal that treatments that target the CD28 co-stimulatory molecule will also affect on-going immune responses.
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