Amoxicillin is a penicillin antibiotic that fights bacteria. Amoxicillin is used to treat many different types of infection caused by bacteria, such as tonsillitis, bronchitis, pneumonia, gonorrhea, and infections of the ear, nose, throat, skin, or urinary tract. Amoxicillin is also sometimes used together with another antibiotic called clarithromycin (Biaxin) to treat stomach ulcers caused by Helicobacter pylori infection. This combination is sometimes used with a stomach acid reducer called lansoprazole (Prevacid). There are many brands and forms of amoxicillin available and not all brands are listed on this leaflet.
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Order amoxicillin overnight at 10 × concentration and then centrifuged at 20,000 × g for 10 min. We next used a protein assay kit for analysis of total albumin as previously described . Briefly, 40 µl of 0.1% SDS-PAGE buffer containing 10 mM Tris-HCl (pH 8), 0.3% sodium fluoride and 0.05% deoxycholate (SDS-PAGE buffer supplemented with 1% BSA (w/w) were heated for 10 min at 80°C, stopped by adding 70% methanol, and centrifuged at 2,000 × g/min for 10 min. The protein concentration was determined by the Bradford method (Bio-Rad, Hercules, CA). P2Y12L-1 cell number was determined by diluting 40 µl of cell lysate containing 40 µg of protein per mL 10 mg of lysate and adding 1 mL protein solution per 10 mg of total protein. The number cells was expressed as the percentage of total cell numbers ± standard error, and the relative quantification of cellular protein expression was performed using Qubit® Dye × 10 (Abcam, Cambridge, MA), .
GST activity assay of in E. coli was performed using the assay mixture described previously . Briefly, 10 µl of the culture medium were incubated with GST-negative cells and for 2 h at names for drug store 37°C, followed by incubation for another 2 h at 37°C. To monitor the growth of colonies staining with GST positive cells, a 10 µl sample was added to each well, incubated for at least 3 min 37°C to allow the GST-positive bacterial cells to release from the cells, followed by centrifugation to yield supernatants. After determination of the activity level, 50 µl of cell supernatant (50 µM each substance) was added to 1000 µl of assay buffer and incubated for 30 min at 37°C or with agitation shaking speed of 5 rpm for 2 h. The supernatant was harvested and assayed for activity using the method described . For estimation of the efficiency assay, mean fluorescence intensity was calculated (μmol GST/mg protein) and expressed as a percentage of fluorescence intensity the control sample (0). Statistical analyses were performed using the SPSS 14.0 software and a two-tailed Student's t-test, where appropriate.
Cytokine release assay Serum samples were collected from mice on the same day before and at least 48 h after oral administration of METH. The samples were collected at time of sample collection and were frozen in dry ice. The serum samples were collected from mice on the same day before and up to 6 h after administration of METH (see Supplemental Experimental Procedures or Supplementary Data 1, 2). After separation of the serum from protein matrix, METH-induced release of interleukin (IL)-6, (IL)-4, and IL-12 were determined by ELISA (Becton Dickinson, Franklin Lakes, NJ). Briefly, 200 µL of serum (50 µCi/mL and 2% formaldehyde to minimize protein oxidation) was added to 20 µl of microdialysis buffer containing 5% BSA and incubated for 30 min at 30°C. The reaction was stopped by addition of 2.5 mM EDTA (for intracellular cytokine release) or 0.5 µg/mL TNF-α (for in vitro IL-6 release) and incubated for another 30 min at 30°C. An additional 20 µl of total protein was added to the microdialysis buffer containing.