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Inhibitors were applied previously in the corresponding samples and preincubated for 1 hour.
The insets of Figure 5 a-1) and (b-1) show the SEM images of the corresponding samples, and those of Figure 5 a-2) and (b-2) show the enlarged graphs between 9 and 11 KeV.
IL-12p40 secretion wasecretionzed for the corresponding samples and quantified by ELISA.
Intracellular staining was performed by adding rabbit anti-CD44 (Epitomics, USA) to the corresponding samples and stored on ice.
If ELISPOT results indicated ≥ 500 sfc/106 PBMC, the corresponding samples and controls were processed for flow cytometry.
Extracellular staining was performed by adding a mouse-anti CD24 antibody (courtesy of Prof. Mina Fogel, Kaplan Medical Center, Israel) to the corresponding samples and stored on ice.
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The corresponding sampling and reconstruction procedure is shown in Fig. 7.
Blue represents genera with higher abundances in the corresponding sample, and white represents genera with lower abundances.
Variances for the profiles were calculated by adding and scaling the corresponding sample and buffer variances.
For each study entry, there are many Experiment entries and corresponding Sample and Run entries.
The alternative alleles were present in the corresponding sample, and absent in the control sample obtained from an unrelated individual.
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