1) SCID Murine
M43开放阅读框
2) Open reading frame
开放阅读框
1.
Cloning of hepatitis C virus open reading frame sequence and non structural protein expressions of the virus;
丙型肝炎病毒整个开放阅读框序列的克隆及各组分蛋白的表达
2.
The efficiency impact of the individual s length was analyzed,Open Reading Frame(ORF) filter was designed to modify the coding region dynamically based on the evolution progress of the best individual,and the effectiveness of ORF filter was demonst.
对此,分析了个体长度对GEP求解效率的影响;设计了开放阅读框(ORF)过滤算子根据最优个体的进化历程动态调节个体的有效编码区域;验证了ORF过滤算子的有效性,实验结果表明,在同样的进化代数内,引入ORF过滤算子,GEP能进化出更高适应度的最优解且减少平均运行时间17。
3) ORF
开放阅读框
1.
The genome of 1867bp and an open reading frame (ORF) of 1047bp were amplified by PCR and RT-PCR.
为了解G蛋白β亚基基因的作用方式,本文根据同源物种G蛋白β亚基相关序列设计引物,通过PCR(polymerase chain reaction)和RT-PCR(reverse transcriptase PCR)技术,获得了以水稻为寄主的立枯丝核菌G蛋白β亚基(G-protein beta-subunit of rice Rhizoctonia solani,简写gbrrs1)的基因序列和开放阅读框ORF(open reading frame)(GenBank登录号EU267677)。
2.
Methods:Bioinformatics approach is applied to analyze the promoter,ORF,translation initiation site,protein hydrophobicity and domain in dystrophin with exons3-7 deletion.
方法:用生物信息学方法对dystrophin基因3-7号外显子缺失后可能的启动子、开放阅读框、翻译起始位点、蛋白疏水性性质改变及重要结构域进行分析。
4) open reading frame
开放阅读框架
1.
Methods Nested RT-PCR was used to amplify the whole length of mRNA and open reading frame of FHIT gene .
方法运用巢式RT-PCR扩增FHIT基因全长和开放阅读框架及PCR扩增FHIT基因3-9外显子。
2.
Based on the position weight matrix(PWM) and length distribution of open reading frame(ORF),a simple method for predicting translation initiation sites is presented.
结合位置权重矩阵(PWM,position weight matrix)和开放阅读框架(ORF,open reading frame)的长度分布特征建立了简单的方法识别翻译起始位点,此方法能很好地区分上游AUG和TIS。
3.
Dual coding is a phenomenon which refers to a mature mRNA that contains two open reading frames(ORFs) in the same direction to code two different proteins.
双重编码(dual coding)是指一段mRNA序列同方向上存在两个开放阅读框架,从而可编码不同氨基酸序列的现象。
5) Open reading frame
开放阅读框架(ORF)
6) exon open reading frame 15
15号外显子开放阅读框
1.
Methods Mutation analysis was carried out by polymerase chain reaction and direct sequencing of all exons,including the mutation hot spot-exon open reading frame 15(ORF15)and exon/intron boundaries of retinitis pigmentosa GTPase regulator(RPGR)gene.
方法应用聚合酶链反应-直接测序,检测与XLRP相关基因视网膜GTP酶调节因子(retinitispigmentosaGTPaseregulator,RPGR)基因的所有外显子和突变热区15号外显子开放阅读框(exonopenreadingframe15,ORF15)及其与内含子交界处序列。
补充资料：龙井43(Longjing 43)
| 龙井43(Longjing 43) 茶树无性系品种之一。从龙井茶树群体品种中单株选育而成。 灌木型、中叶类、早生种。植株较矮，从根颈处分枝，枝叶繁藏。树姿半开张，分枝密度极大。叶枝上斜，叶片呈椭圆形，叶尖钝，叶面隆起，叶色深绿，富光泽，叶较厚，叶质较软。侧脉明显，锯齿细匀，叶缘微波。芽平均长1.58cm，一芽三叶平均长5.05cm，芽粗壮，茸毛中等，嫩叶背卷，色黄绿，在芽柄上泛有红斑，育芽力强。叶层厚，新梢密度很高，在青壮期每0.333平方米有芽1025个。开花结实力一般。扦插成活率高，抗寒性强，适应性广，耐采性强。春茶一芽二叶化学成分含量为：氨基氮4.5mg%，儿茶素116.24mg/g，咖啡碱4.42%，茶多酚19.18%。适制龙井茶和其他绿茶。制成龙井茶，外形挺秀，香高持久，具有狮峰龙井的风格。 |
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参考词条