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1.intravenous inject Evans blue through vena caudalis to observe intestine mucous membrane permeability and vasopermeability;
静脉注射Evans蓝检测肠黏膜与血管通透性的变化;收藏指正
2.Method 8 male SD rat were injected LPS 10 μg/kg(wt) in vena caudalis once,and methylprednisolone 20 mg/kg(wt) i.m. 3 times.
方法雄性SD大鼠8只,尾静脉注射大肠埃希氏杆菌脂多糖(LPS,Lipopolysaccharide)10μg/kg(wt)一次,肌肉注射甲基强的松龙20 mg/kg(wt)三次。收藏指正
3.For BPH group and UM+BPH group, after the BPH model were established, Albumin ultrasound contrast agents were injected into every rat from the vena caudalis plus 1MHz, 1w/cm2 ultrasound prostatic local irradiation by the UGT 1025 gene transfection equipment.
BPH组及UM+BPH组建立模型后,每只大鼠由尾静脉注射白蛋白微泡1ml,并对前列腺局部用UGT 1025型超声基因转染仪以频率1MHz,强度0.5W/cm2进行间歇辐照5min,作用时间10s,间歇10s。 超声辐照后24小时,各组随机取一只大鼠,分离前列腺并用电镜观察血管及细胞膜变化。收藏指正
4.Methods (1) Kunming mice, weighing 35-45 g, were used. Animal models were made by injection of 0.11mol/L t-BHP (1ml/100g weight) into vena caudalis and after 15 min the animals were put into a closed container (0.3L) for 10 min. Then a stroke index score was tallied for each animal.
方法 (1)选用健康昆明小鼠40只,雌雄各半,尾静脉注射0.11mol/L t-BHP (1ml/100g体重),15分钟后将小鼠置于约0.3L密闭容器中10分钟,后取出进行卒中指数评分。收藏指正
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