双重染色时出现假性双标记细胞。
In double staining false double labeled cells appeared in these sections.
将辣根过氧化物酶注入单侧肌肉内，在三叉神经运动核尾侧的腹内侧部引起了双侧的标记细胞。
Unilateral injection of horseradish peroxidase into the muscle resulted in bilateral labelling of cell in the ventromedial region of the caudal trigeminal nucleus.
结果免疫组织化学和双免疫荧光标记结果显示TIMP-1在正常肌肉的血管内皮细胞处表达；
Results The results of immunohistochemistry and double immunofluorescence showed that TIMP-1 was positive in vascular endothelial cells of normal muscles.
采用HRP、WGA-HRP及荧光双标记法，对68只大鼠隔区的主要亚细胞群隔内侧核、隔外侧核、斜角带核、隔三角核和隔微核之间的纤维联系和分支投射进行研究。
The interconnexions and branching projections between the various components of tne septalnuclear complex in 68 rats were studied with HRP, WGA-HRP and fluorescence double labeling methods.
共聚焦扫描显微镜下可见EAAT1与GFAP双标记的星形胶质细胞。
The confocal laser scanning microscopic analysis showed the double staining for EAAT1 and GFAP.
方法采用反复夹闭双侧颈总动脉伴低血压造成拟VD大鼠模型，通过原位末端标记（TU NEL）法检测脑神经细胞凋亡情况。
Method Experimental VD model rats were caused by clipping two side of total artery in neck repeatedly and to examine cerebral neurocyte apoptosis with TUNEL.
采用双标记流式细胞分析技术，分别检测各组小鼠脾脏及肠系膜淋巴结（MLN）CD80M和CD86 M的表达。
The number of CD80/CD86 M of spleen and mesenteric lymph node(MLN) were determined by double-label FCM method.
采用双标记流式细胞分析技术，分别检测各组小鼠脾脏及肠系膜淋巴结（MLN）CD80M和CD86 M的表达。
The number of CD80/CD86 M of spleen and mesenteric lymph node(MLN) were determined by double-label FCM method.
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