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Resin from the courbaril tree.

从孪叶苏木中提取出的一种树脂。

Methods:120 cases of intestinal tract biopsy tissues were carried on tissue fixation,deaquation,transparence,steeping wax,hematoxylin staining and immunohistochemistry using lightwave-microwave combination Ⅱ in lightwave-microwave oven.

选择肠道活检组织120例,组织固定、脱水、透明、浸蜡、苏木精染色和免疫组化染色用光波-微波组合Ⅱ在光波-微波炉中进行,同时以全自动组织脱水机处理组织和常规免疫组化染色作为对照。

The cells from hippocampus, stria-tum, ependyma, thalamus, olfactory bulb, cortex, brain stem and cerebellum of the brain were studied using HE staining and im-munocytochemistry.

应用苏木精-伊红染色和免疫组织化学方法观察人胎脑室管膜下区、海马、纹状体、丘脑、嗅球、皮质、脑干及小脑的Nestin阳性细胞。

Pittosporum skin lotion smoked: Goodeniaceae Paper 30 grams, Speranskia tuberculata, angelica, safflower, hematoxylin, Clematis, Wujiapi, Notopterygium, single live, Angelica, 9 grams of Chuan Jiao.

海桐皮熏洗剂:海桐皮30克,透骨草、当归、红花、苏木、威灵仙、五加皮、羌活、独活、白芷、川椒各9克。

Objective To explore the regulation effect of haematoxylin on immunogenic reaction of rats suffered from UC by serum TLC subgroup, IgG and lysozyme level examination.

目的 通过对溃疡性结肠炎大鼠的血清TLC亚群的检测和IgG、溶菌酶含量的测定,探讨苏木对UC大鼠免疫功能的调节作用。

Methods Cell cultures were harvested and stained with haematoxylin and eosin,to analyze cellular metaphase morphology.

收获细胞经苏木素和伊红染色,观察分裂中期细胞核形态,计算核极分裂象细胞百分比。

Cultured cells were harvested and stained with haematoxylin and eosin to analyze cellular metaphase morphology.

收获细胞经苏木素和伊红染色,观察分裂中期细胞核形态,计算核多极分裂像细胞百分比。

Methods Cell cultures were harvested and stained with haematoxylin and eosin,to analyze cellular metaphase morphology.

收获细胞经苏木素和伊红染色,观察分裂中期细胞核形态,计算核多极分裂象细胞百分比。

Results The CD4(superscript +) 8+ levels in haematoxylin treatment groups was significantly lower than that of models controls. The IgG levels in haematoxylin treatment groups was significantly lower than that of the models group. The level of LSZ was significantly lower than level of model group.

结果 苏木治疗组的CD4/CD8明显低于模型对照组,IgG的含量与模型组比较,12.5 g/kg、25.0 g/kg剂量组明显降低血清IgG水平,LSZ的含量也明显低于模型组,差异有显著性。

HepG2 cells were exposured to oxymatrine, final concentrations of which were 0.1, 0.2, 0.3, 0.4, 0.5, 0.8, 1, 2, 5, 8, 10, 15 g.L-1 respectively, MTT method was used to determine the inhibiting effects of oxymatrine on HepG2 cells proliferation, followed by Haematoxylin and Eosin staining to observe the cell morphology.

以0.1,0.2,0.3,0.4,0.5,0.8,1,2,5,8,10,15 g.L-1的氧化苦参碱处理HepG2细胞,四噻唑蓝法检测其对细胞增殖的影响;苏木精-伊红染色比较细胞形态差异;免疫组化染色进一步检测HepG2细胞肿瘤相关蛋白表达量的变化。

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