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Recombinant adenovirus was identified by polymerase chain reColon cancer cell line SW480 was infected with recombinant adenovirus Ad-p27mt, and expression of p27 protein was detected by Western blot.of expressed p27 protein after Ad-p27mt transfected colon cancer cell.novirus framework plasmid pAdeasy-1 with pShuttle-CMV-hp27mt, 30%combinant adenovirus DNA contained the target gene.

Ad-p27mt的聚合酶链反应检测Ad-p27mt转染大肠癌细胞后的p27mt的表达。结果:①用含pShuttle-CMV-hp27mt转化含pAdeasy-1的超感受态BJ5183后,可获得约30%的阳性重组质粒。②聚合酶链反应检测表明重组腺病毒DNA中含有目的基因。重组腺病毒滴度为7.95×1015pfu/L。

To generate recombinant adenovirus expression vector of human Sema4C gene and observe its expression in mouse myoblasts cell line C2C12 for ensuring easy access to investigate the role of Sema4C gene during myogenesis.

利用Ad5腺病毒载体系统构建人Sema4C基因重组腺病毒表达载体并在成肌细胞系C2C12中表达,并初步探讨Sema4C基因在成肌发育过程中的可能作用。

Recombinant adenovirus containing major outer membrane protein gene of Chlamydia psittaci of chicken origin were successfully constructed with human adenovirus type 5 vector which lack El and E3 genes.

利用E1和E3缺失的人腺病毒5型载体,首次在国内外成功构建了含有鸡源鹦鹉热衣原体主要外膜蛋白基因的重组腺病毒

p53 recombinant adenovirus vector has been constructed and can be used for further research.

成功构建了p53重组腺病毒,为进一步研究p53重组腺病毒的功能提供了条件。

Objective: To construct eukaryotic expression vector of adenovirus type 5 fiber gene and investigate its expression in eukaryotic cell .

目的 :构建腺病毒纤维蛋白基因的真核表达质粒,并检测其在真核细胞中的表达,为腺病毒靶向性载体构建创造条件。

Methods Ten mature Wistar rats were divided into normal control group (5 rats) and adenovirus (E1, E3-Deleted and carried math1 and enhanced green fluorescent protein report gene, Ad-Math1-EGFP) scala vestibuli transfer group (5 rats). Right ears of the Ad-Math1-EGFP transfering group rats were deliveried 5μl Ad-Math1-EGFP (physical tite 2.1×10^11v.p./ml) into cochleas through the way of drilling scala vestibuli of cochlear basal turn. As a control, the normal group received nothing to inner ear. In order to estimate functional condition of vestibule and cochlea, the click-evoked potentials on the surface of the cervical dura mater, auditory brain stem response and swimming time were recorded in all rats at 7 days after treatment, and then histologic and morphologic observation were carried out after animals were sacrificed. Results All animals' morphologic observation showed that inner ear hair cells were normal after transfer.

将10只成年Wistar大鼠分为正常对照组和缺失E1、E3基因片段且构建有Math1基因和绿色荧光蛋白报告基因的复制缺陷型腺病毒(adenovirus-Math1-enhanced green fluorescence protein, Ad-Math1-EGFP)前庭阶导入组,每组5只,实验组大鼠在右耳通过耳蜗底回前庭阶打孔的方法导入物理滴度为2.1×10^11v.p/ml的上述腺病毒5μl,对照组大鼠不做任何处理。7天后对动物进行颈髓硬膜外短声诱发电位(click-evoked potentials on the surface of the cervical dura mater, CDM-CEP)、听性脑干反应阈值检测和游泳试验,评价前庭和耳蜗功能,然后将动物处死进行组织形态学观察。

Dissociated cells were plated onto poly-d-lysine-coated coverslips and propagated in medium containing recombined Wnt3a-adenovirus. Plenty of Nurr1 were detected by RT-PCR after 3 days.

将神经干细胞分为4组,对照组、抗坏血酸诱导组、Wnt3a重组腺病毒诱导组(Wnt3a组)以及Wnt3a重组腺病毒加抗坏血酸诱导组(Wnt3a+AA组)。

Full length LMP2A cDNA was firstly incised from pGEM-T-LMP2A with EcoR Ⅰ, Sma Ⅰ digestion, and then inserted into eucaryote. expression plasmid pCIcc controlled by CMV promoter. The CMV-LMP2A-SV40 expression unit was digested by ClaI, and inserted into E1-substituted adenovirus vector pAx1cw. Then the LMP2A recombinant adenovirus vector was cotransfected into 293 cells together with EcoT22I digested Ad5-TPC.

将带有LMP2A cDNA的重组质粒pGEM-T-LMP2A用EcoR Ⅰ、Sma Ⅰ双酶切下LMP2A cDNA,并将其插入含同样酶切位点的真核表达质粒pCIcc中,使其受控于CMV启动子下;用ClaI切下CMV-LMP2A-SV40表达单元,插入E1、E3区替代的腺病毒载体pAX1CW,选择正确的克隆pAX1CW-LMP2A与Ad5 DNA-末端肽复合体共转染293细胞,通过同源重组获得复制缺陷型的重组腺病毒(Ad5-LMP2A)。

The Centers for Disease Control and Prevention says a recent research report: showed that Ad14 is a rarely reported but emerging serotype of adenovirus that can cause severe and sometimes fatal respiratory disease in people of all ages, including healthy young adults.

疾病控制和预防中心称一份最近的研究报告表明:腺病毒14是腺病毒罕见而新发的变体,它可以在各个年龄段包括健康的年轻成人中导致严重的有时甚至致命的呼吸道疾病。

The replicative recombinant adenovirus is more effective than the replication defective adenovirus used generally at present in replicative ability, oncolytic ability and the expression of exogenous gene in the tumor cell.

构建的复制型重组腺病毒在肿瘤细胞内的复制能力、溶瘤特性和外源基因的表达明显优于目前广泛应用的复制缺陷型重组腺病毒

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