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The surface-active molecule must be partly hydrophilic (water-soluble) and partly lipophilic (soluble in lipids, or oils).
This is because, for every reaction, one or more bonds of a molecule must be broken and new bonds formed.
The molecule must be replicated many times (a step called amplification) and also labelled with fluorescent tags.
An important application of this method is DNA sequencing in which the order of the four nucleotides (adenine, cytidine, guanine, and thymidine) in an oligonucleotide molecule must be determined.
To make a two-qubit computer, the spins of two atoms in every molecule must be controlled; to make a three-qubit computer, three must be controlled, and so on.
First, the molecule must be captured in and traverse a layer of mucus, in which the endings of the receptor cell are bathed; these are known as perireceptor events.
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Therefore, the possible reactions and interactions among molecules must be strictly controlled to prevent incorrect computations.
Thus, the difference in polarity of these molecules must be impacting the vapor pressure dramatically.
The new molecules must be designed to fit into biological receptor sites like a key in a lock.
When metabolic changes are required in a cell, however, certain of these complex molecules must be broken down, and this energy barrier must be surmounted.
Since many therapeutics and reporter molecules must be internalized for activity, crossing the plasma membrane is essential.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com