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1
Control nonischemic limbs were injected with phosphate
buffered
saline
or remained noninjected.
2
The control and OGD groups were given an equal volume of phosphate-
buffered
saline
.
3
Phosphate-
buffered
saline
and human IgG1 antibodies against fluorescein isothiocyanate were used as controls.
4
Thirty-six SCI rats were implanted with labeled and unlabeled MSCs and phosphate-
buffered
saline
.
5
Control mice were untreated or received injections with phosphate-
buffered
saline
.
6
Controls were not treated or received ip injections of phosphate
buffered
saline
(PBS).
7
Similarly constituted control groups received the vehicle alone (phosphate
buffered
saline
)
at the same volume-dose.
8
Control animals received phosphate-
buffered
saline
only.
9
Control mice received phosphate-
buffered
saline
injections.
10
Nissle1917 or phosphate-
buffered
saline
were orally administered for 10 days.
11
The contrast-to-noise ratio (CNR) relative to a phosphate
buffered
saline
tube was calculated for each contrast agent.
12
When compared with phosphate-
buffered
saline
(PBS)-treated mice, the weight of mice treated with mAbs tended to decrease.
13
The extracellular surface of the gap junction cell-to-cell channels was imaged in phosphate-
buffered
saline
with an atomic force microscope.
14
These rats were randomly divided into a human ASC-treated group and a phosphate-
buffered
saline
(PBS) control group.
15
Methods: NS seed extract was prepared in phosphate-
buffered
saline
(PBS), and proteins were precipitated using 80% ammonium sulfate.
16
For surface inoculation, bacteria were suspended in phosphate
buffered
saline
,
sputum from CF patients, or sputum from persons without CF.