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Methods: Mice bearing in vivo transplanted tumor-H22 hepatic carcinoma were used to evaluate the drug"s activity of anti-tumor and GAPSGF"s efficacy enhancing effect by calculating the ratio of antitumor and q. HE dyeing was applied to observe the tumor"s morphological changes after the anti - tumor drug. It is observed the change of theperipheral white blood cells in serum and the body weight to analyze the GAPSGF"s toxicity reducing effect on the anti - tumor drug-Cytoxan. Applying ELISA method to observe the change of IL-2 in serum ,Applying carbon clearance method to test the function of uninuclear phagocyte,took the weight of the spleen and thoracic gland, analyzed the mechanism — efficacy enhancing and toxicity reducing of GAPSGF.

构建体内动物移植性H_(22)肝癌模型,通过计算抑瘤率与q值来分析药物的体内抗肿瘤活性,判断树舌多糖GF注射液的增效作用;采用瘤组织常规HE染色观察药物作用下的肿瘤细胞形态变化;观察外周血WBC数和体重改变来分析树舌多糖GF注射液对环磷酰胺抗肿瘤的减毒作用;采用ELISA法测定血清IL-2、小鼠碳粒廓清法测定单核吞噬细胞功能、取胸腺与脾脏称重测定脏器指数等以分析树舌多糖GF注射液增效减毒的作用机制。

Imported from Taiwan Knittingóú, professional production and processing all types of dyeing printing polar fleece, fleece, one side velvet, ant cloth, cut plush, lamb, towel cloth, single-sided cloth, double-sided cloth, sweater fabric, compound fabric, jacquard air layer, health cloth, all kinds of mesh fabric, terry cloth, rib.

公司引进台湾产针织大圆机,专业生产加工各类染色印花摇粒绒,双面绒,单面绒,蚂蚁布,剪毛绒,羊羔绒,毛巾布,单面布,双面布,卫衣布,复合布,提花空气层,健康布,各种网眼面料,毛圈布,罗纹。

Oral administration of DNA nanoparticles synthesized by complexing pCMVβ DNA with chitosan,which modified with gelatin,Sodium Alginate,PEG and acetylize respectively,resulted in transduced gene expression in the intestinal epithelium.

分别使用明胶、海藻酸钠、PEG及乙酰化修饰包裹含LacZ的质粒pCMVβ的壳聚糖纳米颗粒,通过口服发送后经X-gal染色检测目的基因在小鼠体内的表达。

The authers fetched the embryo calvarial peristeum tissue, got human osteoblast by enzyme-assimilating methods and tissue-block culture methods. We observed the morphological change, growth feature and osteogentic capability, of osteoblast during culture in vitro with phase contrast invert microscope, drew the growth curre and identified the cells by alkaline phosphatase dye. At same time, the morphology and bioactivity of 3-5th-generation osbeoblast and anabiotic cells was studied comparatively. 2. titanium particles were examined by scanning electron and the size was determined by semi-automated image analysis. The 3-5 th gereration of human osteoblast were cultured in medium with different concentration of particulates titanium alloy (1mg/ml, 0.1mg/ml, 0.01mg/ml). Cell growth and proliferation was detected by MTT method after 2、4、6 days that particles were added into medium and ALP activity was measured by kit after 4、7、10 days respectively. 3. With above same methods,the 3-5th generation of human osteoblasts were cultured for 3、6、9days after different concentration of particulates titanium alloy (1mg/ml, 0.1mg/ml, 0.01mg/ml) were added into the medium and OPG gene expression was quantified by RT-PCR.

1、取人胚胎颅骨骨膜,采有用酶消化法和组织培养法获取成骨细胞体外培养并传代,观察细胞形态,生物特点及成骨特性,并绘制生长曲线同时碱性磷酸酶染色鉴定成骨细胞以及比较冻存前3-5 代与冻存后成骨细胞的特点。2、电镜下观察钛合金颗粒的形态并测量其粒径,将不同浓度的钛合金颗粒(1mg/ml,0.1mg/ml,0.01mg/ml)与成骨细胞共同培养,分别于第2、4、6 天用MTT 法测量细胞增殖情况及4、7、10天用试剂盒检测碱性磷酸酶活性。3、分别将不同浓度的钛合金颗粒(1mg/ml,0.1mg/ml,0.01mg/ml)与成骨细胞基因培养3、6、9 天用RT-PCR 方法半定量测定骨保护素基因mRNA 的表达。

The location and structures of sex-pheromone-producing gland in female H.insularis were studied by EAG,GC,SEM,and TEM.These studies showed that thegland situate in the intersegmental membrane between the eighth and ninthabdominal segments,and is an eversible abdominal fold;Many plump cones disturbon the surface of the gland.The glandular cells of 2-day old virgin female H.insularis are arranged in one layer,among which the central cells are columnarepithelial cells and flat on two sides.The nucleus is irregular elliptical.There isevident conjugation between cells and the involution is more in the basal membraneof cell.Microvilli are distributed on the cytoplasmic membrane and linked withendocuticle on which there are many layers of chitin,and the outer cuticule is staineddeeper.The cell contains bubbles,mitochondria,glycogen deposits,roughendoplasmic reticulum and smooth endoplasmic reticulum.

结合触角电位、毛细管气相色谱、扫描电镜、透视电镜等技术对小线角木蠹蛾雌蛾腹尖末端不同组织部位提取物的测定分析以及腺体位置和形态结构的观察发现:小线角木蠹蛾性信息素分泌腺位于腹部末端8~9节之间,是一个由节间膜特化而成的上皮结构,为一可外翻的腹褶,腺体表面分布着饱满的锥形体,羽化后2天未交尾的雌蛾腺体细胞呈单层排列,腹面中央由密集的柱形上皮细胞组成,细胞排列向两侧延伸至背部,其形状由柱形逐渐变为扁平形,细胞核为椭圆形,细胞与细胞间有明显的胞连接,细胞基底膜基褶较多,质膜上分布着微绒毛,并与内表皮连接,内表皮上有多层几丁质,外角质层染色较深,细胞质中含有空泡、线粒体、脂质粒、粗面内质网和光面内质网。

Now has all dyeing, weaving and finishing production systems stereotypes, according to the requirements of customers proofing and production goods, the current major products :4-20 MM VONNEL and the BOA plush fabrics, SOFT BOA, 6-15 MM all color particles cloth ,20-110 MM HIPE cloth, TUMBLING, acrylic and wool blended fabric, pure wool fabric, scissors stuffed, double shear stuffed, CVC shearing fabrics, knitted shearing fabrics, knitted cashmere shearing cloth embossed / printed cashmere, pearls Cashmere Mies Cashmere, PV Cashmere, Peacock cashmere, fleece, coral cashmere, double-sided coral cashmere, superfine cloth-lun, monthly production 800,000 yards, its products are widely applied to toys, handicrafts, handbags, luggage, shoes, cars, chairs, sitting kit winter snow caps, home textiles supplies , leather, clothing, children's clothing, baby clothing, fashion, jacket, at such.

目前已具备染色、织布和定型整理生产系统,可按客户的要求进行打样和生产大货,目前主要产品有:4—20MM VONNEL和BOA长毛绒布、SOFT BOA、6—15MM各色颗粒布、20—110MM HIPE布、TUMBLING、腈纶和羊毛混纺布、纯羊毛布、剪毛绒、双面剪毛绒、CVC剪毛布、超柔剪毛布、超柔剪毛布压花绒/印花绒、珍珠绒、密斯绒、PV绒、孔雀绒、摇粒绒、珊瑚绒、双面珊瑚绒、超细边纶布等,月产量80万码,其产品广泛适用于玩具、工艺品、手袋、箱包、鞋、小汽车坐椅、坐套、冬季雪帽、家纺用品、皮衣、服装、童装、婴儿服装、时装、茄克,羽绒服等。

Methods: After transferred pcDNA3.1/hTM plasmid into rabbit artery by high-pressure injection, rabbit common iliac artery were cut and anastomosed again. At the 14 days and 28days after second operation, we checked inside diameter of anastomotic stoma and blood flow velocity by color Doppler. The treated artery were sliced and stained by Verhoeff. Local neointima formation and the ratio stenosis of intervascular were calculated by computer.

用注射式加压转染的方式对兔动脉壁转染pcDNA3.1/hTM质粒,再制造动脉损伤-阻滞模型,于术后14天、28天用彩色多普勒观察活体吻合口内径和血流流速;再做病理切片Verhoeff染色,观察血管内膜增生的程度、部位,计算血管内膜面积、中膜面积和血管狭窄率。

For TEM, there were classical chatacteristics of cell apoptosis, which was bridge structure disappeared, cell withered , chromosome aggregated and broken and there was bubbles in cell.

透 射电镜下可见桥粒结构消失,细胞萎缩,胞内出现大量的空泡,染色质边集,断裂等,出现凋亡的典型特征。

Methods Fourteen mutated vpr fragments were selected from patients with HIV. Both eukaryotic expression vector pcDNA3.1 and PCR products were purified, double-cut by Hind Ⅲ and BamH Ⅰ, and the cut products were legated and transformed into competent cells JM109. The 14 reconstructed plasmids were transfected into Hela cells. Cells with pcDNA vpr-wt, pcDNA vpr-Fs and pcDNA3.1 blank cells, and without pcDNA3.1 cell were established.

以14个带有HIV-1vpr基因片段的PcD-NA3.1真核表达载体构建重组质粒,将其转染Hela细胞,并设立保守株vpr基因转染细胞、突变株vpr-FS基因转染细胞、空载体转染细胞和未转染细胞作为对照,经逆转录多聚酶链式反应检测目的基因转染成功后,Pi染色,用流式细胞仪检测被转染细胞的细胞周期分布和细胞凋亡率。

Methods 14 mutanted vpr fragments selected from Chines patients with HIV. Both eukaryotic expression vector pcDNA3.1 and PCR products purified , double-cut by HindⅢ and BamH and the cut products legated and were into competent cells JM109. The 14 reconstructed plasmids electronically transfected into hela cells, and established cells with pcDNA vprwt 、pcDNA vpr-Fs and pcDNA3.1 blank cells, and without pcDNA3.1 cell.

将14个带有HIV-1 vpr基因片段的pcDNA3.1真核表达载体构建重组质粒,将其转染Hela细胞,并设立保守株vp r基因转染细胞、突变株 vpr-FS基因转染细胞、空载体转染细胞和未转染细胞作为对照,经RT-PCR检测目的基因转染成功后,经Pi染色用流式细胞仪检测被转染细胞的细胞周期分布和细胞凋亡率。

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