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- Sequence analysis showed that the deduced amino acid sequence of the fragment was the most homologous to G6pdp of Kluyveromyces lactis(62.7%). And it was confirmed that the partial CgZWF encoding glucose 6-phosphate dehydrogenase was cloned. 基因序列分析表明;此片段编码的氨基酸序列与Kluyveromyces lactis的G6pdp同源性最高(62.;7%25);表明已经得到编码葡萄糖6-磷酸脱氢酶的目的基因片段。
- The amino acid sequence analyses of STCs and cDNAs have revealed that reduced STCs (monomer) consist of 179 (chum salmon),223 (coho salmon) and 231 (Australian eel) amino acid residues,respectively. STC单体的氨基酸序列分析表明,大麻哈鱼、银大麻哈鱼和澳大利亚鳗鲡的氨基酸残基数分别为179、223和231个。
- Keywords bovine cementum attachment protein;amino acid sequence analysis; 牛牙骨质附着蛋白;氨基酸序列分析;
- The N-terminal amino acid sequence analysis of bovine cementum attachment protein 牛牙骨质附着蛋白N末端氨基酸序列分析
- The extraction and N-terminal amino acid sequence analysis of porcine enamel matrix proteins 猪釉基质蛋白的提取及N末端氨基酸序列分析
- Cloning and Amino Acid Sequence Analysis of the Cysteine Proteinase Inhibitor Gene in Gossypium hirsutum 陆地棉巯基蛋白酶抑制剂基因克隆及其氨基酸序列分析
- The nucleotide sequence analysis showed that ATCC27853 shared 98% alignment with PA103. The mutations in amino acid sequence are: Asn-364 to Ser; 测序表明,ATCC27853与PA103核苷酸同源性为98%25,产生了7个碱基的突变,突变碱基导致第364位的天冬酰胺变成丝氨酸,第506位的丝氨酸变成色氨酸,第515位的丝氨酸变成甘氨酸。
- Isolation and purification of somatolactin and its N-terminal amino acid sequence analysis from Japanese sea bass (Lateolabrax japonicus) 鲈鱼生长催乳素的分离纯化与N-末端序列分析
- Cleavage site amino acid sequence is 112 R R Q R 116 R 117 F. 其裂解位点的氨基酸序列为112R-R-Q-R-116R-117F;
- The bioinformatics analysis of cucumber CCH Gene1 Using BLASTp for cucumber CCH Amino acid sequence aligment. gov/blastp,经过比对,挑选出15个与黄瓜CCH氨基酸序列相似性相对较高的序列。 这些序列来源于拟南芥、番茄、马铃薯、水稻、大麦、杨树、车前子、酵母、鱼类、犬类、人类。
- amino acid sequence analysis 胺基酸顺序分析
- Nucleic acid sequence analysis showed it contained a 363 integrate ORF, encoding 120 amino acids. It was named gcI. And gcI is located at human chromosome10q21-22. It is up regulated in gastric cancer tissue. 3条为新的EST序列,其中1条获得cDNA全长序列,具有完整的读码框,编码120个氨基酸,命名为gcI,定位于染色体10q21-22。
- Based on the cloning of their parts and the analysis of homology of their genetic nucleotide sequence and deduced amino acid sequence, primers of internal standard DNA of gene AcrA. and AcrE were designed and synthesized. The internal standard of AcrA. 在克隆AcrA、AcrB部分基因片段并进行基因及编码蛋白的同源性分析的基础上,设计合成构建AcrA、AcrB的内标准DNA所需引物,经过3次(12个)PCR成功地合成了AcrA、AcrB的内标准DNA。
- Methods: Acetic acid was selected to extract the enamel matrix proteins. The N terminal amino acid sequence of enamel matrix proteins were determined with SDS-PAGE electrophoretic and blot membrnce analysis. 方法:选择乙酸提取法获得釉基质蛋白,采用SDS-PAGE电泳和印迹膜测序法分析N末端氨基酸序列。
- Genetic code Sequence of nucleotides in DNA and RNA that determines the amino acid sequence of proteins. 遗传密码: 去氧核糖核酸(DNA)和核糖核酸(rna)中的核酸排列顺序能够决定蛋白质里的氨基酸排序。
- The process by which messenger RNA directs the amino acid sequence of a growing polypeptide during protein synthesis. 转录核糖核酸信号在蛋白质化合中引导一个正在生成的多肽氨基酸序列的过程
- Its predicted ORF encoded a 258 amino acid peptide. Sequence analysis in Genbank (http://www.ncbi.nlm.nih.gov) revealed the protein was belong to a domain unknown function 26 (DUF26) family of receptor-like kinases in plants. 对该蛋白进行同源性比较发现,其含有2个C-X8-C-X2-C基序(Cys-rich repeat, CRR)即半胱氨酸富集区,其中第四个半胱氨酸残基不保守,该基序会形成二硫键,编码两个未知功能的DUF26(Domain Unknown Function 26)结构域。
- Its molecular mass is approximately 33 000 Dalton withN-terminal amino acid sequence NH_2 - N- P - C- Y- L- G-S-F-Q-T. SDS-PAGE电泳检验结果表明,一种同工酶得到了纯化,定名为MjGLU1,分子量为33KD左右,其氨基端氨基酸序列为NH_2-N-P-C-Y-L-G-S-F-Q-T。
- Note:The lower left is nucleotide sequence homology and the upper right is amino acid sequence homology. 注:左下方为核苷酸序列同源性,右上方为氨基酸序列同源性。
- Sequence analysis revealed that the full-length SNC73 cDNA is 1651 bps in size with an open reading frame of 1152 bps encoding an immunoglobulin a-1 molecule of 494 amino acid residues(Genbank:AF067420). 而SNC73基因为32个克隆之一,其cDNA全长为1651个核苷酸,共编码494个氨基酸(Genbank登录号为:AF067420)。