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Latent viral load in the spleens of infected mice was quantified by real-time PCR using the ABI 7300 Real Time PCR System (Applied Biosystems, Foster City, CA).
Latent viral load in the spleens of infected mice was quantified by real-time PCR using the ABI 7300 Real Time PCR System (Applied Biosystems, Foster City, CA, USA).
The degree of vascular albumin leakage from cremasteric venules of Mac-1-/ and wt mice was quantified as described previously by both our laboratory [18] and others [19], [20].
Interaction between the male and female mice was quantified by manual annotation of video recordings in which the behaviors were categorized as sniff body, approach, chase, walk away, mount and attempt mount, thrust and/or ejaculation, or non-interacting.
Progression of metastases in hormone-free or hormone-replete mice was quantified weekly by whole-body bioluminescent luciferase imaging (BLI).
Clearance of Aβ after intracerebral injection of antibody into Tg2576 mice was quantified by Aβ immuno-staining.
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Body weight and tumour volume of all mice were quantified 3 times per week.
The tumor sections with immunopositive regions from control and treated mice were quantified for intensity, size and area using Ariol software Review Station.
GC levels in liver, lung, and spleen from 9 V/null and WT mice were quantified by LC/MS-MS (Lipidomic Core, University of South Carolina).
The absence of effects on adiposity between control and LON mice were quantified by determinations of body weight and composition as shown in Fig. 1B and Table 1.
Trophic shifts of the mice were quantified by the differences in the proportional contributions of each trophic group to the mouse diets between populations that received resource pulses and those that did not.
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