核苷酸序列分析表明所克隆基因分别为抗体轻、重链可变区基因。
The nucleotide sequence analyses indicated that the cloned genes coded the variable light and heavy chain domains from mouse antibodies respectively.
研究结果表明，这个长度热点突变区的核苷酸序列分析是研究小麦与山羊草叶绿体基因组之间遗传变异关系的一个非常有效的途径。
The results indicate that the sequence analysis of the hotspot region is a very powerful tool to investigate genetic variations of chloroplast genome in Triticum and Aegilops.
方法：对原发性高血压伴胰岛素抵抗患者胰岛素受体基因酪氨酸激酶域外显子17、18基因突变进行检测，并对突变的外显子进行核苷酸序列分析。
Methods: Using PCR SSCP, we detected the mutation of INSR tyrosine kinase domain exon 17 and exon 18 in 33 primary hypertension patients and 28 normal persons.
使用 DNASIS程序分析核苷酸序列并推导氨基酸序列。
DNASIS program was used to analyse the nucleotide sequence and deduce the amino acide sequence.
核苷酸序列与氨基酸同源性分析表明该片段较为保守。
Sequence analysis showed that homology of nucleotide and amino acid of ts was high.
序列分析结果表明，库尔勒香梨分离物外壳蛋白基因由582个核苷酸组成，编码一个由193个氨基酸组成的蛋白质。
The sequence analysis determined that the CP gene of Kuerle pear isolation comprised 582 nucleotides and encoded 193 amino acids containing consensus of nucleotide binding motif.
DNA序列分析表明，T7溶菌酶基因的核苷酸序列与国外发表的序列有99.5%的同源性，推测的氨基酸序列完全一致。
DNA sequence analysis showed that the nucleotide sequence of T7 lysozyme gene was 99.5% homologous with the reported sequence and its deduced amino acid sequence was the same as reported.
对两个片段核苷酸和氨基酸序列进行了同源性分析。
The homologous analysis of two fragments was also accomplished.
通过互联网对测序获得的核苷酸序列进行同源性分析 ，并预测新基因编码蛋白质的结构与功能。
The positive clones were sequenced and the sequence data were analyzed using Nucleotide BLAST software of NCBI and Expert Protein Analysis System of Swiss Institute of Bioinformatics.
并对核苷酸和编码氨基酸序列进行了分析。
其中碳末端45 0个核苷酸的序列测定和分析提示，该7株病毒为麻疹野病毒H1基因型。
Sequence analysis of 450bp of C-terminus of the N gene indicated that all of the 7 isolates were H1 genotype.
对分离到的HEV71阳性分离株进行VP1编码区基因扩增，核苷酸序列测定和同源进化分析。
And identified HEV71 isolates were performed by gene amplification of VP1 coding region, nucleotide sequencing and homology analysis of evolution.
对分离到的HEV71阳性分离株进行VP1编码区基因扩增，核苷酸序列测定和同源进化分析。
And identified HEV71 isolates were performed by gene amplification of VP1 coding region, nucleotide sequencing and homology analysis of evolution.
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