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Homology of sequence of SST and sequence published in Genbank is 99%.

测序结果与GenBank公布的洋葱SST基因氨基酸同源性为99%。

The result showed the homology of nucleotide sequence and amino acid sequence with VEDEVAC strain was 100%.

对克隆片段进行测序，并与其它已发表的BVDV毒株进行比较，进行同源性分析。

At home and abroad published the same 24 NDV sequence homology analysis showed that the nucleotide sequence homology of 80%-98.4%, and amino acid homology of 87.2%-98.2% in between.

与国内外发表的24株 NDV 相同序列的同源性分析表明，其核苷酸序列的同源性在80％－98.4％之间，氨基酸同源性在87.2％－98.2％之间。

The homology of nucleotide sequence was analyzed with DNAsissoftware. The result showed that the homology was up to 99％compared with publicated sequence.

应用DNAsis软件对其序列进行同源性分析的结果表明，上述基因与GenBank中发表的该基因序列同源性均为99％以上。

A eukaryotic expression plasmid composed of the Hst signal peptide sequence in-frame with the human aFGF sequence was used.

有人aFGF序列的信号肽序列在里面结构被使用的Hst的镇静的一真核细胞的表情plasmid。

A method for detecting the presence of a target nucleic acid sequence in a sample, said method comprising subjecting said sample to an amplification reaction using a set of nucleotides, at least one of which is fluorescently labelled, contacting amplification product with a probe under conditions in which the probe will hybridise to said target sequence, said probe comprising a reactive molecule which is able to absorb fluorescence from or donate fluorescent energy to said fluorescent labelled nucleotide and monitoring fluorescence of said sample.

一种用于检测在某样品中是否存在目标核酸序列的方法，该方法包括：使用一套核苷酸对所说的样品进行扩增反应，其中至少一个核苷酸是被荧光标记的，在探针与目标序列杂交的条件下使扩增产物与探针混合，所说的探针包括一种活性分子，该活性分子能够从荧光标记核苷酸吸收荧光或向其贡献荧光能量，及检测样品的荧光。

According to the sequence of the hydrolase gene, we designed the primers to clone the unknown sequence by rapid amplication of cDNA ends.

根据筛选所获得的其中一个阳性克隆水解酶基因的序列，设计引物，通过cDNA末端快速扩增的方法扩增基因的未知序列。

Anti-histidine-tag antibody is usually used for identification of expression of the recombinant protein expressed using pRSET-A. A pair of primers that contained flanking hydropathic amino acid codons were synthesized, to amply the sequence coding for 10~34 aa in the precursor sequence.

质粒pRSET-A是一个常用的高效原核表达载体，编码一N端含组氨酸标签（6×His）的34aa前导肽序列，以方便利用抗组氨酸标签抗体鉴定或纯化所表达的重组蛋白。

A pair of primers that contained flanking hydropathic amino acid codons were synthesized, to amply the sequence coding for 10~34 aa in the precursor sequence. The amplified fragment was inserted into pRSET-A to generate the first double repeat of the precursor gene. By utilizing a pair of isocaudamer BamH I and Bgl II sites, and another downstream Hind III site of plasmid pRSET-A, following a series of simple double digestions and ligation of the resulted products, a series of repeat (3, 4 and 6) precursor peptide fragment genes were derived.

本实验设计一对两侧含编码疏水性氨基酸密码子的引物，经过扩增前导序列10~34aa基因序列，并重新克隆入质粒pRSET-A构建串联二聚体后，再利用质粒pRSET-A的BamH I / Bgl II同尾酶克隆位点，经一系列简单的酶切和连接，快速构建这一前导肽中不含组氨酸标签序列的串联多聚体基因，并成功表达其六聚体重组蛋白。

This thesis has made a deep study on lacustrine sequence stratigraphy and its application to oil and gas exploration and development, based upon the latest theory of sequence stratigraphy, limnology and petroleum geology incorporated with sedimentology, geophysics, tectonics, geochemistry, paleontology, paleoecology, ichnology, paleogeomagnatics and mislaneous analytical means.

"济阳坳陷下第三系沙河街组油气层序地层学研究"以层序地层学、湖泊学和石油地质学的最新理论为指导，充分利用丰富的地震、测井、岩心、录井和油藏工程等资料，综合沉积学、地球物理学、构造学、地球化学、古生物学、古生态学、遗迹学、古地磁学及多种分析测试手段对湖泊层序地层学及其在油气勘探开发中的应用进行了深入探讨。

However, as the name（read－only memory）implies, CD disks cannot be written onorchanged in any way.

然而，正如其名字所指出的那样，CD盘不能写，也不能用任何方式改变其内容。

Galvanizes steel pallet is mainly export which suits standard packing of European Union, the North America. galvanizes steel pallet is suitable to heavy rack. Pallet surface can design plate type, corrugated and the gap form, satisfies the different requirements.

镀锌钢托盘多用于出口，替代木托盘，免薰蒸，符合欧盟、北美各国对出口货物包装材料的法令要求；喷涂钢托盘适用于重载上货架之用，托盘表面根据需要制作成平板状、波纹状及间隔形式，满足不同的使用要求。