mutant allele造句
造句與例句
手機(jī)版
- 1 ) the first group of the mutant alleles included b158 , b140 and b173
1 、分離到的第一類突變體等位基因的有b158 ， b140和b173 。 - The nature of all the three mutant alleles of this group is nonsense mutation disrupting the coding region of oxt gene
該組的三個(gè)突變體等位基因的突變都是無(wú)義突變，它們都破壞了。 xt基因的編碼區(qū)。 - There are no obvious difference for the frequencies and genotypes distribution for the mbl gene codon 54 mutant allele between hans and uigurs
10 ，兩民族ggc54gac基因型分布和突變頻率無(wú)顯著差異。 - The sequence result showed that the nature of pygo mutant alleles f66 , f15 - 108 and f126 were nonsense mutation , which probably led to truncated pro
測(cè)序結(jié)果表明其中h個(gè)突變體等位基因f66 ， f15 108和f126均是無(wú)義突變。 - 2 ) measured the survival curves for the cells overexpressing mutant alleles of gpil7p and chosed the proper cu2 + concentration in the medium for inducing
2 ）測(cè)定過(guò)表達(dá)了突變gpi17p細(xì)胞的存活曲線，并確定了培養(yǎng)介質(zhì)中誘導(dǎo)物銅離子的適宜濃度。 - This group of mutant alleles turned out to be a gene encoding a xylosyltransferase , which is an enzyme transfers the xylose from udp - xylose to the serine of the protein core
這一組突變體等位基因編碼一種木糖轉(zhuǎn)移酶- oxt ，這種轉(zhuǎn)移酶能夠?qū)dp -木糖中的木糖轉(zhuǎn)移到核。 - Of the 21 patients conservatively treated between 1975 and 1997 , 12 had diffuse disease ( homozygous mutant alleles ) and 9 had presumed focal disease ( paternal mutant allele only )
1975年至1997年期間接受保守治療的21例患者中， 12例為彌漫性病變（等位基因突變純合子） ， 9例為局灶性病變（僅父系等位基因突變） 。 - By using a vestigial - ga14 to deliver the tissue specific flipase to the wing , a f1 genetic screen was performed . a number of mutant alleles of known or unknown genes were isolated from this fl screen
通過(guò)運(yùn)用vestigial - gal4 ， uas - flp系統(tǒng)把重組酶專一性地傳遞到翅中的新遺傳篩選體系來(lái)進(jìn)行遺傳篩選，由于在f1即進(jìn)行篩選，故稱f1遺傳篩選。 - This group of mutant alleles turned out to be a gene encoding a golgi adenosine 3 ' - phosphate 5 ' - phosphsulfate transporter ( adenosine paps transporter ) . kyte - doolittle hydrophilicity plots showed that sll is a very hydrophobic protein , especially in c terminus
Kyte - doolittle疏水性分析結(jié)果表明，與其它轉(zhuǎn)運(yùn)子相似， sll蛋白是一個(gè)疏水性很強(qiáng)的蛋白(尤其在它的c端) 。 - 3 ) the 3rd group of mutant alleles included f66 , f15 - 28 , f126 and f107 . these alleles showed wing and cuticle phenotypes related to wg signaling pathway . this group of mutant alleles turned out to be a new component of wg singaling pathway
這組的突變體等位基因編碼一個(gè)wg信號(hào)傳導(dǎo)途徑組成成分干gg由其特點(diǎn)是在n端含有一個(gè)核定位信號(hào)mls ） ，而在c端則含有一個(gè)pho結(jié)構(gòu)域（一種c4hc3鋅指結(jié)構(gòu)） 。 - It's difficult to see mutant allele in a sentence. 用mutant allele造句挺難的
- This study focused on three groups of mutant alleles from mutant alleles of unknown genes . all these three groups of alleles related to either wingless ( wg ) signaling pathway or hedgehog ( hh ) signaling pathway ( each group composed of 3 - 4 mutant alleles )
從該f1遺傳篩選中分離出了很多已知基因的突變體等位基因，其中包括了那些與wingless ( wg )信號(hào)傳導(dǎo)途徑和hedgehog ( hh )信號(hào)傳導(dǎo)途徑相關(guān)的突變體等位基因。 - By analyzing the wing phenotype , cuticle phenotype of germline clone embryo , deficiency kit mapping , direct sequencing and searching the genome sequence database , three genes : sll , oxt and pygo were identified ( each gene corresponding to one group of mutant alleles )
并通過(guò)綜合分析翅的形態(tài)，生殖系克隆胚胎的表皮形態(tài)，以及缺失作圖，直接測(cè)序和搜索基因組數(shù)據(jù)庫(kù)，鑒定出了三個(gè)基因，這三個(gè)基因分別對(duì)應(yīng)于該三類突變體等位基因。 - Genome dna of all blood samples were extracted by using erythrocyte lysis solution and pcr buffer / nonionic detergent / proteinase k . a 109bp fragment was amplified from the human genome dna . 2 . in 166 han samples , 19 ( 11 . 45 % ) heterozygous genotypes of codon 54 mutant allele were found by pcr - sscp
用紅細(xì)胞裂解液和pcr緩沖液非離于去污劑蛋白酶k兩種自配試劑成功地提取了所收標(biāo)本的人白細(xì)胞基因組dna ，并以此為模板成功擴(kuò)增出預(yù)期的109hpmbl目的基因片段。 - By using single strand conformation polymorphism analysis of polymerase chain reaction ( pcr - sscp ) , the frequency of codon 54 mutant allele of mbl structural gene in the population of hans was investigated . 3 . the molecular beacon ( mb ) hybridization technique with visual monitoring was established
建立聚合酶鏈反應(yīng)單鏈構(gòu)象多態(tài)性分析inglestrandconforma tlonpolymorphlsmanalysisofpol仰erasechainreactionproduction ， pcr sscp ）方法，初步調(diào)查漢族人群mbl基因ggc54gac突變情況。 - The nature of the mutant alleles is either nonsense mutation or the mutation which disrupted the splicing of the primary transcripts . anti - en antibody staining and in situ hybridization on sll germline clone ( glc ) embryo using wg antisense probe showed defective en protein bands and defective wg transcripts bands
通過(guò)對(duì)sll生殖系克隆胚胎進(jìn)行的抗engrailed ( en )抗體染色和wg反義探針的原位雜交結(jié)果表明，與野生型果蠅的胚胎相比較， en蛋白和wg轉(zhuǎn)錄物條帶出現(xiàn)了明顯的缺失。 - To construct eukaryotic expression vector of mbl gene with codon 54 point mutation , the target sequence in pgem - mbld plasmid , which conains mbl cdna with codon 54 mutant allele , was amplified by pcr . after the cdna fragement and plasmids pci - neo were prepared by digestion with sma i and sal i , the fragment was inserted into sma i and sal i site in pci - neo eukaryotic expression vector , and the recombinant vector , named pci - mbl54 , was obtained . the pci - mbl54 , digested with restriction enzymes , was found to contain the point mutation mbl cdna by agarose gel electrophoresis analysis
本實(shí)驗(yàn)以ggc54gacmbl突變?yōu)檠芯繉?duì)象，選用真核表達(dá)質(zhì)粒pci - neo ，根據(jù)已構(gòu)建好的含54位密碼子突變型mbl基因t載體的結(jié)構(gòu)，設(shè)計(jì)合成新的引物， pcr擴(kuò)增54位密碼突變型mbl基因，凝膠回收，雙酶切pcr產(chǎn)物和pci - neo質(zhì)粒， t4連接酶連接，將前者克隆至后者的sma和sal位點(diǎn)，轉(zhuǎn)化大腸桿菌xl - 1blue ，氨芐選擇培養(yǎng)。 - ( 3 ) we further demonstrated that the atcull component of scfco11 complexes was modified via axr1 . mutations axr1 resulted in reduction of the modified atcull component of scfcol1 complex . ( 4 ) the mutant alleles of axri ( axr ] - 3 and axr ] - 12 ) showed moderate insensitivity - to ja - inhibitory root growth and mild reduction of ja - inducible gene expression of atvsp , thi2 . i and pdfi . 2 compared with that of wild type
以表達(dá)融合蛋白flag - coi1的axr1基因突變體axr1 - 3為材料，用- flag抗體進(jìn)行免疫共沉淀分析發(fā)現(xiàn)， scf ~ ( coi1 )復(fù)合體中修飾的atcul1蛋白的含量明顯降低，表明axr1基因突變影響對(duì)scf ~ ( coi1 )復(fù)合體中修飾的atcul1蛋白的修飾。 - Whereas their parent mutant axr1 - 3 was male fertile , showed moderate insensitivity to ja - inhibitory root growth and mild reduction of ja - inducible gene expression ; parent mutant coi1 - 2 - was a leaky mutant allele of coi ! , it exhibited reduced ja insensitivity and partial fertility . - taken together , all these results suggested that scfcoil complex was required for the ja response and that the axr1 - dependent rubl modification of atcull subunit of scfcol " was important for ja signaling in arabidopsis
試驗(yàn)結(jié)果發(fā)現(xiàn)， coil 2 axrl 3雙突變體在根的生長(zhǎng)、茉莉素誘導(dǎo)基因的表達(dá)和雄性育性方面對(duì)茉莉素都表現(xiàn)為完全抗性；而親本coil 2和axrl三突變體對(duì)茉莉素均表現(xiàn)部分不敏感性，表明axr基因和coil基因的同時(shí)突變協(xié)同增強(qiáng)擬南芥對(duì)萊莉素的不敏感性， axr基因與coi基因相互作用調(diào)控茉莉素的信號(hào)傳導(dǎo)途徑。
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