Uniformly 13C,15N-labeled 13C,15N-labeledepared by IsoLife (Wageningen, The Netherlands) using the following protocol.
They were trained to follow the script using the following protocol.
Bone marrow cells were obtained from Nrf2 knockout animals purchased from the Jackson laboratory and were subsequently differentiated in macrophages using the following protocol.
The three databases were preprocessed using the following protocol [6, 31, 32]: (1).
In order to measure the bacterial killing efficiency of the samples, the remaining bacteria were collected again using the following protocol.
All mixtures were digested using the following protocol.
For immunohistochemical studies, paraffin sections were rehydrated to PBS and processed using the following protocol.
The β-galactosidase units produced per minute were estimated using the following protocol.
Three images per field were recorded, and a total of 1030 cells were analyzed using the following protocol.
The mitochondria in live GFP-expressing animals were stained with the MitoTracker dye (Invitrogen) using the following protocol.
Immunohistochemical staining was performed on lung and nasal turbinate tissues to detect viral N protein using the following protocol.
