1) fae operon gene
fae结构基因
1.
Objective:To clone and express fae operon gene clusters from enterotoxigenic Escherichia coli(ETEC) K88ac fimbriae in vitro,and to study the bioactivity of recombinant fimbriae from fae gene clusters expression.
目的:在体外克隆和表达猪肠产毒性大肠杆菌(ETEC)K88ac菌毛操纵子fae结构基因,并检测重组菌毛的相关生物学活性。
2) gene structure
基因结构
1.
It was reviewed that new progresses of gene structure,enzymology,fermentation and application studies on microorganism inulinase.
综述了微生物菊粉酶基因结构、酶学性质、发酵生产与应用等方面研究的最新进展。
2.
In this study, the bovine ACAD8 full-length mRNA and genomic DNA sequence were obtained and its gene structure was determined through alignment of the genomic DNA sequence to the mRNA sequence.
本研究中获得了牛的ACAD8基因的mRNA和基因组DNA序列并通过基因组DNA与mRNA的比对确定了其基因结构。
3.
The gene structure, biological functions and application in diseases of kallikreins are reviewed.
本文综述了激肽释放酶的基因结构特点、生物学功能并重点介绍其在疾病中的应用。
3) Structural gene
结构基因
1.
Study on variation of parts of structural genes of 4 infectious bronchitis virus isolates from China;
4株IBV中国地方分离株部分结构基因变异的研究
2.
Objective To sequence and analyze the structural gene of dengue virus type 2 strain GD06/93 isolated from Foshan, Guangdong province, in order to understand the molecular epidemiology of dengue virus and the development of dengue virus vaccine.
结果GD06/93株结构基因序列长度为2325bp,编码775个氨基酸。
3.
According to the published type 1 pili nucleotide sequence from human Escherichia coli,a pair of primers were designed and synthesized,which localize conservative regions of type 1 pili structural gene and were modified with Bam H I and Hin d Ⅲ enzyme sites.
根据人源大肠杆菌 1型菌毛结构基因 (pilA)DNA序列 ,在其保守区设计了 1对带有 BamHI/Hind Ⅲ酶切位点的引物 ,经PCR扩增 ,从 2 4株鸡源大肠杆菌致病株染色体中得到 2 1个大小约 6 5 7bp的阳性产物 ,经酶切、连接、转化及筛选 ,得到 3种来自不同血清型鸡源大肠杆菌 (O1、O78及O88)PCR产物的阳性克隆。
4) Genomic structure
基因结构
1.
To study the regulatory mechanism of Vsx1 expression,we analyzed the genomic structure and intron polymorphism of goldfish Vsx1 by PCR.
结果表明:金鱼Vsx1基因由5个外显子和4个内含子组成,与斑马鱼、人、小鼠的Vsx1基因结构相同。
2.
To determine the genomic structure of human PRPSAP1 gene encoding the PAP39 subunit of phosphoribosylpyrophosphate synthetase(PRS) complex,the End Trimming and Cassette Ligation(ETCL)PCR method was applied.
PRPSAP1基因结构的确定有助于进一步研究人PRPSAP1基因的功能。
5) structure gene
结构基因
1.
Construction,identification and expression of three kinds of shuttle plasmids of adenovirus expression vector of hepatitis C virus structure gene;
3种丙型肝炎病毒结构基因腺病毒载体穿梭质粒的构建鉴定及表达
2.
Structure genes C,E1,E2 and partial 5 UTR of HCV were amplified and cloned by long RT-PCR in single step,which was demonstrated by sequencing.
利用长RT PCR技术 ,一次性克隆出HCV的结构基因C、E1、E2及部分 5’UTR ,经测序 ,验证了其正确性。
补充资料:FAE
分子式:
CAS号:
性质:固态、液态、气态或混合态燃料(可燃剂)与空气(氧化剂)组成的爆炸性混合物。目前主要采用液态燃料,有环氧乙烷、环氧丙烷、硝基甲烷、硝酸丙酯、硝酸肼、二甲肼等。可充分利用大气中的氧,因而大大提高了单位质量装药的能量,使用时,将燃料装入弹中,送至目标上空引爆,杀伤和破坏面积大,具笼罩性,能摧毁一般弹药摧毁不了的目标,且可产生一定的窒息作用。为常规兵器开创了既减轻重量又提高爆炸威力的途径。用于装填集束炸弹、航空炸弹、反舰导弹、水中兵器和火箭弹。
CAS号:
性质:固态、液态、气态或混合态燃料(可燃剂)与空气(氧化剂)组成的爆炸性混合物。目前主要采用液态燃料,有环氧乙烷、环氧丙烷、硝基甲烷、硝酸丙酯、硝酸肼、二甲肼等。可充分利用大气中的氧,因而大大提高了单位质量装药的能量,使用时,将燃料装入弹中,送至目标上空引爆,杀伤和破坏面积大,具笼罩性,能摧毁一般弹药摧毁不了的目标,且可产生一定的窒息作用。为常规兵器开创了既减轻重量又提高爆炸威力的途径。用于装填集束炸弹、航空炸弹、反舰导弹、水中兵器和火箭弹。
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