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Briefly, the granules shown in this study (labeled as "Calcium Granules") were prepared by adding sterile solutions of either 0.25 M CaCl2 and/or 0.25 M Na2HPO4 (both at pH 7.4) to FBS (2.5 ml) at final concentrations of either 48 mM CaCl2 (used for Figs.
Additional file 2: Coexpression modules identified in this study labeled numerically and in color.
Across all N/E-ergic brain areas imaged in this study, labeled LDCV sections measured diameters in the range of 70 to 650 nm, with only 2.5% of the population smaller than 120 nm).
While precise mapping of the injection sites to anatomically identified ganglia was not performed in this study, labeled axons were traced running through ganglionated plexuses without making any apparent synaptic contact until reaching an apparent target zone where dense innervation of neighboring ganglion cells occurred.
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In this study, label-free relative quantitative proteomics was employed to screen differently expressed membrane proteins in CD4+ T cells from active VKH patients and normal controls.
The two transgenic lines used in this study label myeloid leukocytes, most likely neutrophils.
The microtubule gliding velocities of various mutants tested in this study (labels and scale bar are indicated).
The chemical data sets used in this study are labeled on the basis of the described encoding.
In this study, we labeled the surface proteins of mouse ES (mES) cells with membrane-impermeable biotins and then purified the proteins by streptavidin affinity purification.
Luminal tumors from this study were labeled luminal-H, H for Horlings.
All orders investigated in this study are labeled by an asterisk.
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