PMC

(A) The room chosen to be an arthroscopy laboratory, equipped with a tap with running water, drain in the ground, adequate lighting, and sockets for 110 and 220 volts. (B) A large bucket used to capture the arthroscopy water, and the pleasure pliers fused to a vise. (C) Water tap with its original tip. (D) Adapters are necessary to be able to attach the arthroscopy serum set to the water tap. (E) Water tap without its original tip. (F) Water tap with the first adapter that will allow the attachment of the serum. (G) Arthroscope serum equipment attached to running water tap with all adapters. (H) The arthroscopy serum attached to the water tap working. (I) The bovine coupled to the pressure pliers, a large bucket used to capture the arthroscopy water, and the surgical instrumental table water tap being prepared to couple the arthroscopy serum equipment. (J) Pressure pliers fused to a vise.

Temporal structures of visual-tactile stimuli in PLWs. Here, two of the eight experimental conditions of Experiment 1 are shown. The upper figure shows the “tactile leading” temporal condition, in which one tap was leading 150 ms to one visual footstep (visually touching the ground), while the other tap was synchronous with the second visual footstep. In contrast, the lower figure shows the tactile lagging condition, in which one tap was lagging 150 ms to one visual footstep while the other tap was synchronous with the onset of the second visual footstep. V, visual; T, tactile feedback (tap); L, left; R, right.

Bacterial detection in assay buffer (n = 3), tap water (n = 9), and ground water (n = 9). For detection in buffer, each bacteria in ten-fold serial dilution was incubated with its corresponding capture (5 min) and detection (15 min) antibody and spun at 8000 RPM for 1 min through density gradient. For detection in tap and ground water, 20 ml of tap or ground water were spiked with bacteria and concentrated using VivaSpin columns. Corresponding buffers were added for each bacteria and the assay were performed as explained earlier. The fluorescent signal was quantified using fluorescent microscopy. The normalized fluorescence for negative control sample is represented by concentration 100 CFU/ml.

Build concept for tap testing mechanism.