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Thus, when ordinary salt (sodium chloride, formula NaCl) is dissolved in water, it forms an electrolytic solution, dissociating into positive sodium ions (Na+) and negative chloride ions (Cl-), whereas sugar dissolved in water maintains its molecular integrity and does not dissociate.
The capsular material can be isolated essentially free of LPS, is phenol and proteinase K resistant, ethanol precipitable and does not dissociate in sodium dodecyl sulfate.
Complexes of ADAMTS5-2 and TIMP-3 formed in the presence of Bio-PPS also bound to streptavidin Sepharose beads, indicating that PPS remains associated with the high-affinity ADAMTS5-2 TIMP-3 complex, and does not dissociate after complex formation.
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In this regard it has an unrivaled capacity to hold in solution an exceptionally wide range of substances, including electrolytes (salts, which dissociate into ions in aqueous solution), colloids (particulate matter small enough to remain suspended in solution), and nonelectrolytes (substances such as glucose that retain their molecular structure and do not dissociate into ions).
It is usual when the functional groups are primary ketones, aldehydes, alcohols, or esters, because these groups are electrically neutral and do not dissociate in the pH range of 2 12.
As expected, septin-Gic1 complexes were stable and did not dissociate.
The benzoic acid cocrystal is the only one that exhibited a higher solubility (21 μg/mL) and did not dissociate.
As α1-antitrypsin polymers are known to be extremely stable and do not dissociate even in the presence of high concentrations of urea [ 9, 55], this disparity is not the result of dissociation during electrophoresis.
Whereas, e.g. amyloid cores in Tg2576 and APP23 mice are completely soluble in SDS solutions with EDTA, human amyloid deposits are much more stable and do not dissociate in the presence of ionic or nonionic detergents or strong denaturing agents like guanidine hydrochloride.
Herein we use the expression 'stable protein complex' to describe multi-protein assemblies that have long half-lives (sometimes being considered 'permanent' as they assemble shortly after synthesis of the subunits and last throughout the subunits' lifespan) and do not dissociate in the test tube unless subjected to strong denaturing conditions.
These results suggest that in stored cytosols, recruitment of procaspase-9 to the apoptosome is not significantly diminished but the molecular timer [12] is dysfunctional such that recruited procaspase-9 does not undergo auto-processing, and thus, does not dissociate from the apoptosome.
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