"Maybe I know the difference between apolar and unipolar ganglions but that's about all."

Because of this the process is limited to apolar inks that are soluble in ethanol.

Ordinary alkenes are not susceptible to a nucleophilic attack (apolar bond).

As in the V80E structure, a network of salt-bridges surrounds the apolar core.

It also has higher compaction capacity than the other phospholipids, because the apolar tail is less bent.

Pentamer formation of water and alcohols in apolar solvents.

Alkanes are the least reactive class of hydrocarbons due to their apolar sigma bonds.

The hydrophobic nature of the pocket favours aromatic and apolar substrates over highly polar ones.

If a reversed order of running of the compounds is desired, an apolar stationary phase should be used, such as C18-functionalized silica.

Similarly, the terms omniphobic and omniphilic apply to both polar and apolar liquids.

The 16-cell stage is the first stage at which two cellular phenotypes (polar and apolar) can be distinguished (discussed in Section 4.1).

Surfactant or surfactant mixture forms reverse micelles when mixed with an apolar solvent.

The polar side (with the hydroxyl group) interacts with the solvent leaving the apolar to the catalyst surface.

G and G is the difference in solvation energy for apolar and polar groups, respectively, when going from the unfolded to the folded state.

Small uncharged apolar molecules diffuse through lipid bilayers many orders of magnitude faster than ions or water.

The organogelators precipitate out as fibers, forming a 3-dimensional network which then immobilizes the apolar solvent to produce organogels.

If an apolar cell is transplanted to the outside during the 8-32 cell stage, that cell will develop as a trophoblast cell.

This process leads to the development of two different populations of cells: Polar cells on the outside and apolar cells on the inside.

The run of four buried apolar residues which distinguishes the G-to-A strand transition in CD4 is absent.

The portion entering the membrane, referred to as the head, is usually apolar and hydrophobic, this produces an energetically favorable insertion of the Pore-forming toxin.

Other reactions with apolar reactants such as Ene reactions and Diels-Alder reactions also exhibit rate accelerations.

The interface between the two monomers is narrow and well defined, consisting of neutral or apolar amino acids, suggesting the hydrophobic interaction is important for dimerization.

As a good apolar aprotic solvent, 1,2-dichloroethane could be used as degreaser and paint remover but is now banned from use due to its toxicity and carcinogenity.

GROMOS force field (A-version) has been developed for application to aqueous or apolar solutions of proteins, nucleotides and sugars.

Lasalocid is able to make neutral complexes with monovalent and divalent cations and transport them through apolar phase (including lipid bilayer membranes).