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For control purposes, a scrambled sequence of 26RFa (Sc-26RFa) and normal saline (1 ml) were injected.
To develop H22 tumors, 107 H22 cells (0.1 mL) were injected in the right axillary region of each mice.
100 sporozoites in a total volume of 1 ml were injected IV on the day of challenge.
Depending on the infecting microorganism, 106 (E. coli) or 104 (P. aeruginosa) CFU contained in 0.1 mL were injected into each thigh of anesthetized mice.
PC-3 cells (2×106 cells as a 50% suspension in matrigel, Becton Dickinson, Bedford, MA) in a final volume of 0.1 ml were injected subcutaneously at right flank of Balb c nude mice.
The protein samples (3 ml) were injected into the focusing chamber of the Microrotofor cell Bio-Rad Laboratories Inc , Hercules, CA) using a 3 ml syringe until all ten compartments were equally loaded.
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200 μl of vinblastin (250 μg/ml) were injected (I/P injection) to animals 45 minutes before they were sacrificed in order to block the dividing cells in metaphase.
GV-1.4 viral particles (0.1 ml at a titer of 1.106 PFU/ml) were injected into 1 day newborn NFS mice.
GBR12909, fluoxetine, or nisoxetine dissolved in distilled H2O/0.9% NaCl (50 50, v/v, 2 mg/ml) were injected intravenously into rats 60 min prior to the injection of [18F]CFT.
Aliquots of P815 cells (~107 cells/mL) were injected subcutaneously into the left inguinal area of mice.
Study Design: On the 16th day of gestation, xanthine (1 mM) and xanthine oxidase solution (0.1 100 mU/ml) were injected into the intrauterine cavity of pregnant rats.
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