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plasmid相关的网络例句

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与 plasmid 相关的网络例句 [注:此内容来源于网络,仅供参考]

F episome, F plasmid 例句 in bafdx, fdx is an element of area → element All I know is that the winner's name begins with the letter F.

我所知道的就是胜利者的名字是以字母F开头的。

Methods HBx gene with EcoR Ⅰ and Hind Ⅲ endoenzyme sites was obtained by using PCR from plasmid pcDNA3.1-HBx.

用PCR方法从质粒pcDNA3.1-HBx中扩增含Kpn Ⅰ和Hind Ⅲ酶切位点的HBx基因序列。

Methods Eukaryotic expression plasmid pCMVCD was constructed , and identified by re2 striction endoenzyme digestion. CD gene was transfected into NSCs from new2born Wistar rats using Lipofec2tamine2000. Positive clones (named NSCs/ CD cells) were screened by G418 presence. 52Fluorocytosine (52FC) ad2ministration of different concentrations were incubated with NSCs/ CD cells. NSCs/ CD cells viability ratios were mea2 sured by MTT assay.

通过构建真核表达质粒pCMVCD ,限制性内切酶消化鉴定后,采用Lipofectamine 2000 脂质体介导法转染新生大鼠室管膜下区神经干细胞(Neural stemcells , NSCs),G418 筛选阳性克隆,加入不同浓度的52氟胞嘧啶(52Flourocytosine , 52FC),MTT比色法测定NSCs的生存率。

Methods The cDNA coding sequencing of enterokinase light chain was amplified by RT-PCR from mouse dodecadactylon mucosa and cloned into pET32a expression plasmid. The recombinant enterokinase light chain was expressed in BL21(DE3) and purified with Ni-affinity chromatography.

采用RT-PCR从C57BL/6J小鼠的十二指肠肠系膜黏膜组织中钓取肠激酶轻链的cDNA,将其克隆入pET32a原核表达载体中,并在大肠杆菌BL21(DE3)中进行表达,然后以镍亲和层析法对表达产物进行纯化。

III For constructing the expression vector of a fusion protein and obtain a target protein with full identity on aa sequence of a natural 13- 1,3-1 ,4-glucanase, with the recombined plasmid DNA harbouring the target gene as template, the primers designed with restriction sites for both terminals and enterokinase recognition site, followed by PCR amplification, was induced to the target gene.

为构建融合蛋白表达载体和获得与天然蛋白质序列完全一致的目的蛋白,以含有目的基因的重组质粒DNA为模板,设计引物时加入两端酶切位点及肠激酶裂解位点,通过PCR扩增引入目的基因中,测序结果表明接头和读框正确。

After thermal induction, no specific recombinant protein band in SDS-PAGE was found, but G-CSF activity was detectable. Therefore, a new recombinant plasmid pBVHG2 expressing hG-CSF hybrid protein with additional 8 amino acids which could be cut off specifically with the help of mucosal enterokinase at the N terminus of hG-CSF was constructed.

含此质粒菌株虽然表达菌体裂解后可测得明显的生物学活性,但SDS-PAGE仍未见特异表达产物带;因此,再应用相同方法,在hG-CSF cDNA突变体5′端增加24核苷酸对的FLAG肽编码序列,构建了hG-CSF杂交蛋白(hG-CSF天然蛋白N末端增加8aa的FLAG肽,后者可由肠激肽酶切除)的表达质粒pBVHG2。

In the Group hIGF, 10 μL ofLipfectAmine-mediated hIGF-1 plasmid was locally injected in sciatic epineurium of the crush spot. Nothing was given as Group S.

结果:术后8周再生神经纤维神经传导速度、复合肌肉活动电位的最大波幅和潜伏期hIGF-1治疗组明显大于模型组和空白对照组(P<0.01)。

Methods The LPL cDNA was isolated from the human epiploon adipose tissue by means of RT-PCR. The LPL cDNA was ligated into the pcDNA3.1Zeo. The recombinant pcDNA3.1Zeo-LPL cDNA was identified by endonucleases, PCR and DNA sequencing. COS-1 cells were transfected with the recombinant LPL gene plasmid using Lipofectamine 20001M The LPL mass in cells and the culture medium were determined by a Markit-M LPL Kit. Spectrophotometry was used to measure the LPL activity.

采用RT-PCR法从人大网膜脂肪组织获取LPL cDNA基因,以pcDNA3.1Zeo质粒作为载体,运用基因克隆技术构建野生型人LPL cDNA重组质粒,限制性内切酶酶切、PCR以及双向测序鉴定重组质粒;运用Lipofectamine 2000将重组pcDNA3.1 Zeo-LPL cDNA质粒导入COS-1细胞,RT-PCR法检测LPL mRNA,ELISA法和比色法分别检测细胞裂解液及细胞培养基中LPL浓度及活性。

The novel primers were evaluated by detecting BTV serotypes 1, 3, 5, 8, 10, 11, 21 and 22. The specificity of the primers was estimated by comparing to gene sequences of viruses published in GenBank, and further assessed by detecting BTV serotype 1-12 and Epizootic hemorrhagic disease virus serotype 1-4. The sensitivity and repeatability of PCR with the novel primers were evaluated by successfully detecting the recombinant plasmid pGEM-T121 containing the diagnosed nucleotide sequence.

Blast软件分析引物与GenBank发表的病毒基因的同源性,显示引物特异性较好;利用8个不同血清型BTV标准毒株进行RT-PCR检测,证实该引物能有效检测不同血清型BTV;通过BTV1-12和EHDV1-4进行检测,证实该引物具有较好的检测特异性;通过制备的含特检序列的质粒标准品P121进行检测,显示该引物检测的敏感性为105 copies,重复检测CV%为0;对模拟血清样品进行检测,结果均为阳性。

The vitro methods include autoagglutination test,calcium dependency test,pyrazinamidase test,salicin fermentation,esculin hydrolysis,Congo red colony test and virulence plasmid.

体外法包括自凝试验、依钙试验、吡嗪酰胺酶试验、水杨苷发酵、七叶苷水解、刚果红菌落试验和毒力质粒。

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