- 更多网络例句与周质体相关的网络例句 [注：此内容来源于网络，仅供参考]
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Recombinant plasmid pSVH 7 DNA of avian influenza virus H7 subtype heamagglutinin gene was encapsulated with DC-chol/DOPE liposomes and PC/chol/SA liposomes separately. Two-week old SPF chickens were intramuscularly inoculated with 50 μ g/0.2ml of the liposome entrapped PSVH 7 DNA. Four-weeks later, each chicken was challenged with 0.1ml 〓 AIV . One week after the challenge, the secretion of the cloacas was collected and transfected to chicken embryos to isolate the virus. The virus was isolated from 6/6 of the control group, 1/6 of the naked DNA group, 1/6 of the PC/chol/SA entrapped DNA group and 0/6 of the DC-chol/DOPE liposome entrapped group. The HI antibody titers (log2) of the four groups were 6. 83±0.98, 7. 0±1. 26, 7. 83±1. 17 and 8. 00±0.89 respectively 1-week after challenge, and 8. 5±0.55, 8. 17±0.82, 8. 68±0.45 and 9. 33±0.54 respectively 2-week after challenge. The results showed that inoculation of liposome entrapped DNA significantly enhanced resistance to virosis in animals.
将含禽流感病毒H7亚型血凝素基因的重组质粒pSVH7用DC-chol阳离子脂质体和胆固醇／卵磷脂／十八胺脂质体包裹，免疫2周龄SPF鸡，4周后用同型禽流感病毒进行人工感染，1周后采集泄殖腔分泌物分离病毒，结果未免疫组6／6分离到病毒，裸质粒DNA免疫组1／6分离到病毒胆固醇／卵磷脂／十八胺脂质体包裹DNA免疫组1／6分离到病毒，DC-chol脂质体DNA免疫组没有分离到病毒（0／6）：人工感染后1周各组的HI抗体（Log2）分别为6.38±0.98，7.00±1.26，7.83±1.17，8.00±0.89，2周后为8.50±0.55，8.67±0.82，8.68±0.45，9.33±0.52，脂质体包裹组在同期均高于未免疫组和裸DNA免疫组，表明脂质体包裹质粒DNA免疫动物后，能增加动物对病毒感染的抵抗力和反应能力。
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HRP was coupled with the fluorochrome FITC and encapsulated with liposome . pEGFP-N1 plasmid (expressing green fluorescent protein) with encapsulation in commercially available liposome was prepared. The eyes were enucleated 1, 4 and 8 weeks after zonule rupture and anterior segments comprising lenses were incubated in medium containing one of these components. Cryo-sections were made and translocation of fluorescent macromolecule from the medium into the lens and green fluorescent protein expression in the epithelium were observed by fluorescent microscopy.
制备FITC标记的HRP脂质体；制备pEGFP-N1质粒（表达绿色荧光蛋白的质粒），并用脂质体包裹；豚鼠悬韧带部分离断后1周、4周、8周取含晶状体的眼前段标本分别在含有FITC-HRP复合物、pEGFP-N1质粒的培养基中孵育，冰冻切片，荧光显微镜观察FITC-HRP复合物进入晶状体和pEGFP-N1质粒在晶状体内表达的情况，比较悬韧带离断侧与非离断侧的差异。3。
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Then the caprine fetal fibroblast cells were transfected with p6.5hLF-EGFP by LipofectamineTM-2000 and selected by G418 for 3 to 4 weeks. The G418 resistant transfectants were identified by PCR and EGFP detection. The results indicated that the transgene was stably integrated into the open region of the chromatin of G418 resistant fibroblast cells.
脂质体介导法转染山羊胎儿成纤维细胞，G418抗性筛选3-4周后，经PCR扩增和报告基因EGFP表达检测，得到稳定整合外源基因的转基因供体细胞系，为制备高效表达人乳铁蛋白的转基因山羊乳腺生物反应器提高可靠的核移植供体细胞。
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The organelles, such as Golgi bodies together with small vesicles, endioplasmic and reticulum play the key role in the formation of the secondary wall of helical tracheary elements in the stem of Cucurbita moschata, though cortical microtubules are correlative with the process as well.
高尔基体及其分泌小泡和内质网等细胞器参与了导管次生壁的形成，其中周质微管也起了一定的作用。
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Encapsulated psoralen were evaluated by dialyzation using psoralen gel as the control. Changes of liposome????encapsulated psoralen and release rate were detected during a 3????week storage at 4 ℃ for evaluating the stability of the liposomal formulation.
以同浓度的补骨脂素凝胶为对照，用透析法检测补骨脂素脂质体凝胶的体外释药模式，并对其在4 ℃下贮存3周的释药稳定性进行研究。
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A diverse range of effects:on protein solubility and secretion was observed,and these effects were highly dependent on the particular chaperone.In the host strain over-expressing chaperone SecB harboroing pSecB,the amount of total periplasmic proteins was increased by about 71％and the activities of alkaline phosphatseand GL-7-ACA acylase(GL7A)were increased by about 54％and l.5-fold respectively.In the host strain over-expressing chaperone GroEL bearing pGroEL,the amount of total periplasmic proteins was increased by 52％,and the activity of penicillin G acylasewas in creased by about 76％;about 90％of Hexameric Calcitonin(Cal6)inclusion body and l5％of MS2interleukin3(MS2-HIL3)inclusion body became soluble respectively.All the data were compared with the parental strains un-bearing plasmdis pSecB or pGroEL.
在过量表达SecB的宿主菌中，周质空间分泌蛋白总量较对照组提高了约71％，GL-7-ACA酰化酶在周质空间酶的活力较对照组提高了约1.5倍，碱性磷酸酯酶在周质空间酶的活力较对照组提高了约54％；在过量表达GroEL的宿主菌中，周质分泌蛋白总量较对照组提高了约52％，青霉素G酰化在周质空间酶的活力较对照组提高了约76％，鲑鱼降钙素六聚体的可落性组分的比例由原来的45％增加到约90％，而MS2-人白介素-3融合蛋白的包涵体有约15％转变为可溶性组份。
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Methods:Prepared multilaminar liposome vaccine by film evaporaqtion combined with lyophilization; Immunized BALB/c mice with the obtained liposomeencapsulated influenza split vaccine and the routine influenza split vaccine, serum antibodies were assayed on weeks 213 by the haemagglutinationinhibition test and ELISA, the HI test for the special antiHA antigen and the ELISA test for the IgG. Protective immunity against intranasal virus challenge was determined at 12 weeks postvaccination.
采用薄膜法与冷冻干燥法相结合的方法制得多层脂质体；用制得的脂质体流感疫苗和普通疫苗分别免疫小鼠，用血凝抑制实验和酶联免疫吸附试验对免后2～13周的小鼠血清的抗体水平进行检测，HI检测其特异性抗体，ELISA检测IgG抗体水平并对小鼠的保护效率进行检测。
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In accordance with the invention, the hG-CSF protein can be prepared with high purity through rather simple process facilitating secretion of large amount of hG-CSF fusion protein into the periplasm, which does not require complicated processes such as solubilization and subsequent refolding required for isolation of the hG-CSF protein produced in cytoplasm as insoluble inclusion bodies by conventional techniques, thus, the hG-CSF protein can be widely used as an active ingredient in the development of supplementary agents for anticancer therapy.
根据本发明，通过促进大量hG－CSF融合蛋白分泌到周质中的相当简单的方法可以高纯度制备hG－CSF蛋白，所述方法不需要复杂的加工过程例如对于通过常规技术分离胞质中产生的作为不溶性包函体的hG－CSF所需的溶解和随后再折叠，因此，在开发用于抗癌治疗的补充药物的过程中可用hG－CSF蛋白广泛地作为活性成分。
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All the transfected and un-transfected rMSCs were attached to Allo-DBMs. These new biomaterials were implanted in muscle bags and segmental radius defects of the New Zealand white rabbits, and some controlled material groups were established for comparison. All the biomaterials and the controlled materials were assessed by gross observation, radiographical and histological methods.
取兔自体骨髓基质细胞培养扩增，用脂质体介导的方法转染人骨发生蛋白2基因，将转染和未转染人骨发生蛋白2基因的自体骨髓基质细胞附和于异体兔脱钙骨基质形成新的生物植骨材料，连同空白及单纯脱钙骨基质对照组植入兔前肢肌袋和桡骨缺损。2、4、6、8周分别取材进行大体，放射线和病理观察。
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During the wall thickening, the number of Golgi bodies increased apparently and cytoplasm was filled with Golgi vesicles. Polylamellate structure of the secondary wall appeard, Along with the further development of tracheary elements, the nucleous disappeared and organelles were decreased, while cortical microtubules were arranged neatly against the inner side of plasmalemma.
初生壁与质膜之间有间隔较规律的次生壁突起；中期，线粒体和高尔基体的数量明显增加，细胞质中几乎充满高尔基体及其囊泡，次生壁中微纤丝已成有序排列；晚期，细胞核消失，导管中央形成空腔，细胞器迅速减少，仅观察到少量高尔基体和线粒体，有大量周质微管沿细胞长轴分布，且在次生壁的周围有大量小泡附着，次生壁的分层结构清晰可见。
- 更多网络解释与周质体相关的网络解释 [注：此内容来源于网络，仅供参考]
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neurofibril：神经原纤维
核周的胞质又称核周质(perikaryon),除含一般的细胞器和发达的高尔基复合体外,还含有丰富的尼氏体(Nissl body)和神经原纤维(neurofibril). 尼氏体又称嗜染质,呈嗜碱性颗粒状或斑块状,电镜下可见由许多粗面内质网和游离核糖体构成,
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perikaryon：核周质
核周的胞质又称核周质(perikaryon),除含一般的细胞器和发达的高尔基复合体外,还含有丰富的尼氏体(Nissl body)和神经原纤维(neurofibril). 尼氏体又称嗜染质,呈嗜碱性颗粒状或斑块状,电镜下可见由许多粗面内质网和游离核糖体构成,
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periplast：周质体
裸藻细胞的最外层是原生质膜,在质膜内,由蛋白质构成周质体(periplast),因此,周质体是细胞的内部构造. 电子显微镜下观察,周质体是由多条壁纹(stripe)密接组成的,这些壁纹螺旋状包围着藻体. 有些种的周质体薄,易弯曲,藻体能变形.
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periplast：[生]质膜,(尤指裸藻的)周质体
crescent screen 月牙筛, 扇形筛 | periplast [生]质膜,(尤指裸藻的)周质体 | trumpetcall 集合号声 紧急召唤
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centroplasm：中心质
蓝藻植物细胞里的原生质体,分化为中心质(centroplasm)和周质(periplasm)两部分. 中心质又叫中央体(central body),在细胞中央,其中含有DNA. 蓝藻细胞中无组蛋白,不形成染色体, DNA以细纤丝状存在,无核膜和核仁的结构,但有核的功能,
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Euglenales：裸藻目
本纲分两个目,即裸藻目 (Euglenales)和柄裸藻目 (胶柄藻目)(Colaciales). 二、裸藻门的代表植物 (一)裸藻属(Euglena) 属于裸藻目. 细胞纺锤形、长纺锤形或圆柱形,前端宽而钝圆,后端锐, 无甲鞘. 周质体的弹性大小,因种而异. 有两根鞭毛,
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ooplast：卵质体
06.092 卵质 ooplasm | 06.093 卵质体 ooplast | 06.094 [卵]周质 periplasm
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periplasm：周质
细胞结构:分为细胞壁和原生质体,原生质体又分为周质(periplasm)和中心质(centroplasm) 图示
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periplasm：(外)周质
peripherin 外周蛋白[一种中間絲蛋白,最初發現于神經元] | periplasm (外)周質 | periplast 周質体
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periplasm：周质;胞外质
periphcricblister蜂窝气孔 | periplasm周质;胞外质 | periplast周质体