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This was a cross-sectional survey of a random sample of older adults selected from using a stratified, multistage sampling method.
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Lymphocytes were selected from PBMC using an immunomagnetic-based selection kit from Miltenyi Bioytec (Auburn, CA).
For single cell PCR individual cells of A. carterae were selected from cultures using a drawn glass pipette on an inverted microscope magnified 100 times.
Responder cells were autologous PBMC or CD8+ T cells (96 98% pure) positively selected from PBMC using anti-CD8 mAb-coated, magnetic microbeads (StemCell).
FSWs were selected from establishments using a convenience sample.
For patients in the study arm, CD34+ cells were selected from aphereses using the Isolex300 device.
Drivers were selected from April 2008 to March 2009 using a stratified multi-stage cluster sampling procedure.
Single particles were manually selected from micrographs using the Boxer interface in EMAN1 (Ludtke et al., 1999).
∼7,000 wild-type particles and 1,000 mutant particles were hand selected from micrographs using Ximdisp (Smith, 1999).
Particles were selected from images using the display program Ximdisp associated with the MRC program suite (Crowther et al, 1996).
Moreover, data were selected from studies using rats in the same age range because aging directly affects the water balance of rats [ 11].
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