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上海希言科学仪器有限公司
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文献和实验was effected in a bare fused-silica capillary 75 μm � 52 cm. The CE-C4 D method was validated with respect to linearity, limit of detection and quantification, accuracy, precision, and selectivity. Calibration curves were linear
PRODUCTION OF COMPLETELY ES CELL-DERIVED FETUSES BY AGGREGATION WITH TETRAPLOID
26G1/2 or 30G1/2 needle; Autoclip applier (Clay Adams B-D 763007); Autoclips (Clay Adams B-D 7631); Mouth controlled pipette; M2 medium; 2.5% Avertin: 2,2,2,-Tribromethanol 2.5 g (Morre-Tec Industries #1693);
In Vivo Luciferin Imaging Procedure
the quantity of needed for an individual experiment. • Syringe filter, 0.2 μM Procedure 1. Prepare a fresh stock solution of Luciferin at 15 mg/mL or 30 mg/kg in DPBS. Filter sterilize through a 0.2 μM filter. 2. Inject 10 μL/g of body weight
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