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Northern crossbreed results showed that it is expressed only in human brain. This gene has a 50% amino acid sequence identity with Caenorhabdilis elegans, Anopheles gambiae sir arid Drosophila, and 94% amino acid sequence identity with Rattus norvegicus and Mus musculus.

Northern杂交结果表明:该基因只在人类大脑组织中表达,且与无脊椎动物线虫、疟蚊和果蝇的同源基因有50%的氨基酸同源性,与脊椎动物大鼠和小鼠的同源基因有50%以上的氨基酸同源性。

The result showed that twocDNA fragments which expressed at high level both in shoot and radicle representedthe gene encoding beta-D-glucosidase; one cDNA fragment expressed specifically inshoot represented the gene encoding mitochondria HSP60; most clones of MF12 andMF17 fragments respectively represented the chloroplast genes encoding prp22 andprp19 proteins which are two components of ribosomal small subunit; while thededuced amino acid sequence from each exceptional one clone was respectivelyhomologous to CDC5 proteins and vesicle-associated membrane proteins; otherthree cDNA fragments expressed preferentially in shoot had no homologue inGenBank.

结果发现2个在胚芽和胚根中表达量都很高的cDNA片段代表的是编码玉米β-D-葡糖苷酶的基因;一个在胚芽中表达而在胚根中不表达的片段代表的是编码线粒体分子伴侣HSP60的基因;片段MFl2的大部分克隆测序结果是与叶绿体基因组中编码核糖体小亚基蛋白prp22的基因同源,但其中有一个克隆测定的cDNA片段序列推测的氨基酸序列与CDC5家族成员有较高的同源性;片段MF17的大部分克隆测序结果与叶绿体基因组中编码核糖体蛋白prp19的基因同源,而有一克隆测定的cDNA片段序列推测的氨基酸序列与参与信号转导的膜结合蛋白VAP27和VAMP有较高的同源性;另有3个优先在胚芽中表达的cDNA片段未查询到同源序列。

Results Same conservative sites and key catalytic sites existed among SjLDH and LDHs from other species. Similarity of SjLDH compared to CsLDH, TvLDH and HsLDH was 75%, 17%, 58%-60% respectively. Phylogenetic analysis demonstrated that the evolution relation between SjLDH and DmLDH was closer than the relation between SjLDH and CeLDH, the relationship between SjLDH and HsLDH-B,-C was closer than HsLDH-A. Three trans-membrane regions were found, the region of 98aa-106aa in three hydrophilia regions located outside of membrane was inferred as the major antigen epitope. This antigen epitope had significant difference with LDHs from protozoon ( Pf ., Tg ., Tv .) and had 1-3 amino acid residue difference with MmLDH, HsLDH-A,-B,-C, and was the same with CsLDH. One of the key catalytic residues and substrate binding loop were located in this region. Tertiary structure demonstrated that 98aa-106aa was on the surface of the protein and formed a substrate binding loop, other two key catalytic sites were at the position near the loop.

结果 SjLDH与其他物种的同源序列含相同的保守位点及催化活性位点,与华支睾吸虫LDH同源性最高为75%,与阴道毛滴虫LDH同源性最低为17%,与人LDH(HsLDH-A,-B,-C)的同源性为58%~60%; SjLDH与果蝇的进化距离较秀丽隐杆线虫为近,3种人LDH中与HsLDH-B、-C的进化距离较HsLDH-A为近;该蛋白具有3个跨膜区域,3个高亲水性区域,主要的线性表位98aa~106aa位于膜外,与原虫LDH相同区域差异显著,而与其他LDH有1~3个氨基酸的差异,关键催化位点之一及底物丙酮酸结合区域位于该区域,蛋白质同源模建分析表明该区域位于蛋白表面形成环状结构,3个关键催化位点位于该区域或在其附近。

compared with the classic rabies virus, the strains shared the higher degree of homology with the street viruses obtained from thailand and philippines than other known strains especially that rabies virus isolated from chiroptera in america.

结果 同源性分析表明, 4株湖南街毒p和m基因核苷酸同源性分别为97.3%~99.4%和98.4%~99.8%;与其它i型狂犬病病毒和疫苗株核苷酸同源性比较,p基因分别为78.4%~90.2%和81.8%~86.8%;m基因的分别为81.8%~92.1%和84.7%~90.6%。4株野毒p和m基因氨基酸同源性分别为98.0%~99.3%和98.5%~99.0%。

Meanwhile, comparison of sequence between AlMV-Ch与AlMV425 show that the homology of the nucleotide and deduced amino acid sequences of the replicase are 97.8% and 97.6% respectively, but the homology of 3'-end un-coding reagin is 98.2%.

AlMV-Ch与AlMV425进行了同源性比较,结果表明复制酶基因编码区核苷酸序列同源性为97.8%,而推测的氨基酸序列同源性为97.6%,3′非编码区的同源性为98.2%。

Amino acid similarities between goat and human were 87% and between gaot and mouse were 83%. Just like other members of FGFs superfamily, FGF5 protein also has a signal sequence ,at same time its protein has higly similar sequence about 120 Amino acid in central core sequence with other breed. Tissue specific expression of the FGF5 gene was also investigated in cashmere goat by RT-PCR analysis. The results showed that FGF5 gene was expressed in different time of the tested skin tissues, including anage and telegon.

结果如下:(1)本研究利用 RT-PCR 方法克隆了羊 FGF5 基因的 cDNA 序列,得到了 925bp的序列,并对该序列进行了分析,与成纤维细胞生长因子家族的成员一样也是由三个外显子组成,也具有一信号序列,成熟蛋白为 270 个氨基酸,经同源性比对得出大鼠与小鼠的 FGF5 氨基酸同源性最高为 97%,在与羊的蛋白质比较中大鼠与羊的同源性为 83%,小鼠与羊的同源性为 84%,人与羊的同源性最高,为 89%。

In order to explain clearly the variation status of embryo from tetrapoid Robinia pseudoacacia and fully use the variation resource initiated in the sexual reproduction of TRP in the further improvement of TRP, the classification and vitalities of seed embryos from tetraploid Robinia pseudoacacia were studied. The main results are as follow. According to the cotyledon number, color and plumpness, the seed embryos of TRP could be divided into 5 types: YVT (yellow, very replete,2 cotyledons), YMT( yellow, more replete,3 cotyledons ), YRF ( yellow, replete,4 cotyledons ), GNT ( green, no-replete, 2 cotyledons ) and WNT ( white, no-replete, 2 cotyledons ).

为了阐明刺槐同源四倍体种子胚变异状况及充分利用刺槐同源四倍体有性过程创造的变异资源对四倍体刺槐进行遗传改良,研究了刺槐同源四倍体种子胚类型及其生活力特征,主要结论如下:刺槐同源四倍体种子胚按照子叶数量、颜色及饱满程度,可以划分出5个类型:黄二、黄三、黄四、绿二及白二,所有类型种子胚混合平均单胚重量接近二倍体的1/2。

Sequences were aligned by BLAST method. Results showed that 309bp fragments shared high similarity with orfl38 in Ogu CMS radish and Brassica cybrids of Ogu CMS radish, which 172 nucleotide sequences and 58 amino acids were same among them. And 689bp fragments shared high similarity (100%) with Pol orf224 in B.napus, which 677 nucleotide sequences and 225 amino acids were same among them.

同源性分析结果表明,利用orf138引物所获得的309bP大白菜mtDNA特异片段均与萝卜Ogu CMS、甘蓝型油菜Ogu CMS萝卜体细胞杂种所具有的Ogu orf138高度同源,二者有172个核苷酸完全相同,有58个氨基酸完全相同;orf224引物所获得的689bP大白菜mtDNA特异片段与甘蓝型油菜的Pol orf224高度同源,二者有677个核苷酸完全相同,有225个氨基酸完全相同,同源性均达到100%。

The sequences were compared with the known sequences in Genbank with BLAST software. P-ACC/M-GGA200 showed 95% homology to a part of AFLP sequence which linked to fusarium head blight resistance gene fragment (AF389881). The P-AGG/M-GGT_(251) has an ORF, and it had homology to a hypothetical protein of Oryza sativa.

根据BLASTn同源性比较,P-ACC/M-GGA_(200)与GenBank中与抗小麦赤霉病连锁的一段AFLP序列(AF389881)同源性达95%;P-AGG/M-GGT_(251)序列中含有一个开放阅读框,根据BLASTp同源性比较,与GenBank中日本栽培稻一未知蛋白(XP 483138)有同源性。

Nested PCR analysis and southern hybridization analysis showed that no polymorphism between H.villosa, Pm97034 and susceptible parent Wan7 107 was detected with the clones from 6VS arm, whereas three clones from H.villosa genome DNA: RH42, RH55, and RH66 showed polymorphism. RGA6 cloned from H.villosa genome DNA was characterized identity to NBS, and show high homology to resistance genes as RPM1 and RPP13 in Arabiadopsis, LRR19 in wheat, and I2C-1 in tomato.cDNA library constructed from T.aestivum-H.villosa translocation line Pm97034 was screened by hybridization with RGA6. Four positive cDNA clones were obtained. R3-2-2 showing 60-90% identity with eukaryotic sulfite oxidases contained an open reading frame of 647bp encoding 140 amino acid, and contained a conserved Moco-dimer domain in the ORF. R6-2-2 showed an ORF containing an Euk-porin domain of 279aa with 20-40% identity to the eukaryotic voltage-dependent anion channel proteins. R8-1-1 showed a complete ORF of 1810bp encoding 493aa with 80-90% identity to plant catalases. R9-1-1 showed an ORF containing a BTB/POZ conserved domain of 204aa with 30-70% identity to pox virus and zinc finger proteins. R3-2-2 and R9-1-1 were the first cDNA clones containingconserved domain of SO and POZ respectively isolated from wheat. R8-1-1 contained a complete ORF with 81% identity to Cat-3. Aspects of the role of R8-1-1 may be same with Cat-3, and it would offer the opportunity for improvement of stress tolerance of wheat.

以RGA6为探针,筛选用抗白粉病小麦—簇毛麦易位系Pm97034构建的cDNA文库,得到了4个阳性克隆。R3-2-2与动植物的亚硫酸氧化酶(sulfite oxidase,SO)有60~90%的同源性,长度为647bp,编码140个氨基酸,具有开放阅读框并含有保守域Moco-dimer.R6-2-2与真核生物的VDAC(voltage-dependent anion chennel)蛋白有20~40%的同源性,长度为1047bp,编码279aa,是一个不完整的开放阅读框,预测结构具有Euk-porin结构域。R8-1-1与植物中已经克隆的过氧化氢酶有80~90%的同源性,长度为1810bp,编码493aa,具有完整的开放阅读框和过氧化氢氧化酶保守域。R9-1-1与动植物的POZ(pox virus and zinc finger protein)蛋白有30~70%的同源性,长度为1446bp,具有开放阅读框和BTB/POZ保守域。R3-2-2与R9-1-1是首次从小麦中克隆到的具有SO和POZ保守域的cDNA序列。R8-1-1具有完整的开放阅读框,与玉米Cat-3基因具有81%同源性,预测R8-1-1可能具有与Cat-3类似的功能,可为转基因小麦抗逆育种提供新的基因。

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