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The characteristic spectra, or light patterns, from the molecules were then studied to determine the structural changes of the molecules.
Additional denatured molecules were then created along the surface of some disrupted fibrils.
The two new hybrid molecules were then tested in a muscle differentiation assay.
Individual DNA molecules were then characterized on the basis of DNA segments that had been joined to make a functional (or nonfunctional) immune effector.
The prepared molecules were then investigated for their anti-inflammatory, ulcerogenicity and analgesic activity in experimental animals.
The DNA molecules were then transfer printed onto a glass slide coated by vapour deposition of 3-aminopropyltrimethoxysilane (APTMS) molecules.
Immunoglobulin G (IgG) molecules were then immobilized on the bilayer system by protein-A – IgG specific interactions.
Similar(4)
Circular DNA molecules are then further enriched by randomly primed rolling circle replication.
Information about the molecules is then transmitted from the receptors to the olfactory bulb in the brain.
The modified oil molecules are then able to stack together much more efficiently, reducing the overall mobility of the liquid.
All molecules are then drawn into the operational folding route by the law of mass action.
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CEO of Professional Science Editing for Scientists @ prosciediting.com