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A liposome formulation was selected for surface modification with polyethylene glycol (PEG), without having any effect on the T1-relaxivity.
However, in cultures, once an infected RBC has been selected for surface expression of a single var, expression is relatively stable in the absence of selection, and the dominant var transcripts can be detected over many generations, while there is a gradual expansion of parasite subpopulations expressing other var [28], [33].
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Nevertheless, there have been some success in circumventing this limitation by inserting reporter genes into lineage-specific gene loci [10] [15], or selecting for surface receptors known to be important in early tissue development e.g. Flk-1 in hematopoiesis and vasculogenesis [16] [18].
Historically, the assumption that the CTC originated from an epithelial solid tumor facilitated isolation and identification technologies that would select for surface markers consistent with epithelial cells, such as the epithelial cell adhesion molecule (EpCAM) [ 3- 6].
Fulfilling the three requirements for freeform surface polishing, the Hilbert fractal curve is selected for freeform surface polishing here.
In this research, AFM was selected for the surface study of Escherichia coli (E. coli) cells, and the shapes and dimensions of the individual bacterium were observed by the AFM topography and phase images.
An AFM instrument (Bruker Nano, Santa Barbara, CA, USA) and a silicon nitride probe with the calibrated spring constant of 0.7 N/m and tip radius of 10 nm were selected for the surface examination of microbial specimens.
Cells oriented perpendicular to the optical path were selected for apical surface area measurements in Slc26a4+/− and Slc26a4−/− mice.
Fifteen volunteers were randomly selected for skin surface profilometry of the crow's feet area.
The NH3 was preferably selected for modifying the surface of PLLA because it can obtain appropriate hydrophilicity and surface energy with high polar component compared to other gases.
Roughly equal numbers of serum samples were selected for hepatitis B surface antigen (HBsAg) positivity and negativity; samples were matched for participant age and gender.
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