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SD相关的网络例句
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Allogene group: SD→Wistar, one group received AVH of cryopreservation, the other group received AVH preconditioned with dendritic cell monoclonal antibodiesdiluted by 1:5 and cryopreserved, and then was treated with DcmAb.

异基因组分别为接受低温保存的AVH移植和接受1:5稀释树突状细胞单抗预处理低温保存,AVH移植后给予DC单抗治疗,同基因组为对照组。

Objective: To investigate the co-cultured allogenic SD rat bone mesenchemal stem cells in vitro, and to perform neural differentiation in vitro.

目的:探讨同种异体大鼠骨髓间充质干细胞在体外的共培养方法,并行神经分化诱导。

Methods: Tissue of rat ovary was obtained from 30 healthy sexually mature non-mated femal SD rats. The rats were divided into two groups (oestrus group and anoestrus group). The expression of α-SMA and vimentin were detected and evaluated by immunohistochemistry and image analysis system in the theca cells of different type follicles.

分别取动情期和非动情期大鼠卵巢,运用免疫组化方法检测肌成纤维细胞的特征性标记和波形蛋白分别在这两组中各级卵泡卵泡膜细胞上的表达情况,并进行图像分析。

Objective To observe the airway remodeling in the respiratory tract of asthmatic SD rats models and the expression of MMP-9/TIMP-1 and compared with the dexamethasone control group in order to find the mechanism of antiasthmatic pills in healing asthma.

目的:通过二次致敏,制成大鼠哮喘模型,探讨气道重塑与MMP-9/TIMP-1表达的关系及平喘丸的干预作用并与地塞米松相对照,力图掀开平喘丸治疗哮喘的机理。

Part Ⅲ: Animal immunization and anticarious experiment of the glucan binding protein B Plasmid pcDNA3. 1 -gbpB DNA vaccine was delivered into Sprague-Dawley rats in two different routes: intranasal and targeted salivary gland immunization . The dynamic variety of specific antibodies in sera and saliva were checked by ELISA.

第三部分 DNA防龋疫苗免疫动物及抑龋实验研究大量制各重组质粒pcDNA3.1-gbpB,分鼻腔滴注组、颌下腺区皮下注射组免疫SD大鼠,并设对照组和空白组,采用ELISA法检测血清及唾液中抗体水平的变化情况。

Methods Sixteen adult Sprague-Dawley rats were enrolled, from which anticoagulative erythrocyte suspension was made, and was incubate with equivalent volume of 1 time,2 times,4 times and 8 times of clinical therapeutic blood concentration of different local anesthetics respectively. Erythrocyte-yeast rossete and Tumor-erythrocyte rosette rate were measured.

选择成年SD大鼠16只,取抗凝血制备成所需浓度的红细胞悬液,与等体积的临床血药浓度、2倍、4倍及8倍临床血药浓度的各研究麻醉药物孵育后,加入补体致敏酵母菌或用自身血浆作为补体来源致敏的肿瘤细胞,测定红细胞、酵母菌花环率和肿瘤细胞-红细胞花环率。

Methods ICH was induced in rats using stereotactic infusion antilogous blood 50μl into the caudate nucleus. The male rats were randomly divided into control group and hemorrhage group. TUNEL method was used to detect apoptosis, and immunohistochemistry method to detect the expression of Caspase-3、 Ref-1 in cerebral tissues at different time.

采取立体定向技术,将SD大鼠自体不凝血50μl注入大脑尾状核区制备脑出血模型,将大鼠随机分为正常组和出血组,分别在不同时间点断头取脑,连续切片作TUNEL、Ref-1和Caspase-3免疫组化染色。

Methods Female SD rats were bilaterally ovariectomized as the ovariectomized obese animal models,observe the effect of the apozem of Achykanthis Bidentataefrom Henan of China on body weight,food intake,serum lipid and Tumor Necrosis Factor-alphain ovariectomized obese rats.

行双侧卵巢切除术制备去卵巢肥胖的动物模型,观察怀牛膝对去卵巢肥胖大鼠体重、摄食、血脂及肿瘤坏死因子-α的影响。

ObjectiveTo observe the effects of Ardisia gigantifolia Stapf extract on blood clotting system and hemorrheology and its mechanism.

目的观察走马胎提取液对血栓病理模型SD大鼠体内凝血系统和血液流变学的影响,以初探其抗血栓的作用机制。

But injury of normal tissue is one of important factors which have to stop killing tumor cell thouoghly, in all process of tunor therapy Since the injury all over argans and cells of the body by free radical, especially significant side-effect to heart via ariblastine ,is universally accepted, we chose Adriamycin as chemical therapy medicine in our study.

由于阿霉素具有比较公认的自由基周身性损伤、特别是对心脏损伤的突出副作用,因此,本课题选择阿毒素作为化疗药物,模型制作采用在SD大鼠肝表面种植Walker-256瘤细胞株,于种瘤后第11天按2mg~(-1)kg体质量给单纯化疗组和化疗保护组的大鼠腹腔注射阿霉素,正常对照组和荷瘤对照组按相同比例腹腔注射生理盐水;同时,每日上午按0.5ml/100g体质量经胃给于化疗保护组抗氧化剂混合液,其余各组每日给于相同剂量的三蒸水;下午按0.1ml/100g体质量经胃给于化疗保护组维生素E溶液,其余各组每日给于相同剂量的处理过的油。

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推荐网络例句

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。

There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.

双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。