chromosomal dna中文是什么意思

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中文翻譯
造句

染色體dna

dna DNA ＝ 1.deoxyribonucle ...
rea of chromosomal dna 染色體dna的rea
chromosomal 染色體的
dna DNA ＝ 1.deoxyribonucleic acid 【生物化學(xué)】去[脫]氧核糖核酸。 2.deoxypentose-nucleic acid 去[脫]氧戊糖核酸。
t dna 轉(zhuǎn)移
t-dna acid]轉(zhuǎn)運(yùn)脫氧核糖核酸; 轉(zhuǎn)運(yùn)脫氧核糖核酸
chromosomal aberration 染色體斷裂; 染色體畸變
chromosomal aberrations 染色體畸變; 染色體異常
chromosomal abnormality 染色體異常
chromosomal abnormallty 染色體異常
chromosomal affinity 染色體親和力
chromosomal aneuploid 染色體異數(shù)體
chromosomal anomaly 染色體異常
chromosomal arm 染色體臂
chromosomal break 染色體斷裂
chromosomal bridge 染色體橋
chromosomal change 染色體改變
chromosomal chimaera 染色體嵌合體
chromosomal contraction 染色體收縮
chromosomal crawling 染色體緩移
chromosomal crossover 染色互; 染色體互換
chromosomal defect 染色體缺失
chromosomal defects 染色體異常
chromosomal deficiency 染色體缺失
chromosomal disease 染色體疾病

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例句與用法

Like mrna, both trna and rrna are transcripts of chromosomal dna .
TRNA及rRNA同mRNA一樣，都是染色體DNA的轉(zhuǎn)錄產(chǎn)物。
Pcr analysis and southern blotting all confirmed that the ced - 9 gene has been integrated into the chromosomal dna of these transgenic plants
對(duì)所得到96株再生苗進(jìn)行pcr檢測(cè)，結(jié)果表明，陽(yáng)性苗比例為34 。
S . tenebrarius chromosomal dna , partially digested with sau3al to yield fragments of 6 ~ 15kb , was ligated with vector pij702
提取黑暗鏈霉菌h6總dna ，經(jīng)sau3ai不完全酶切、凝膠電泳，收集6 15kb片段連接到載體pij702 。
It confirmed that ibdv vp2 gene was integrated into nuclear chromosomal dna by pcr . pcr positve plants were double checked for incorporation of the recombinant gene by southern blots
在轉(zhuǎn)基因組織生長(zhǎng)成植株的過(guò)程中， vp2基因隨著植物細(xì)胞的生長(zhǎng)而得到表達(dá)。
Sequencing analysis showed that the sequence of endoglucanase fragment exhibits 35 % homology with b . subtil is chromosomal dna ( from glyb to apre ) , and 27 % homology with bacillus sp
將此重組質(zhì)粒phchi轉(zhuǎn)化巨大芽抱桿菌b . megateriumap25 ，得到兩株轉(zhuǎn)化子，分別命名為p25113一9 ， p25113一10 。
Bhattacharyya np , basu p , das m , et al negligible male gene flow across ethnic boundaries in india , revealed by analysis of y - chromosomal dna polymorphisms [ j ] . genome res . 1999 aug ; 9 ( 8 ) : 711 - 9
李冬娜、應(yīng)大君、區(qū)采瑩，等.中國(guó)海南島黎族人群y染色體上四個(gè)微衛(wèi)星基因座的多態(tài)性研究.中華醫(yī)學(xué)遺傳學(xué)雜志[ j ] . 2003 ; 1 : 1 - 3
A fusion - trascriptional library was then constructed by inserting sau3ai - partially digested chromosomal dna from 7653r into bamhi cloning site of phn127 . a group of constitutive - expression fusions with different fluorescent strength were obtained
將7653r的總dna經(jīng)sau3ai部分酶解并克隆到phn127上，獲得的融合子庫(kù)，從中篩選到gfp組成型表達(dá)的具有調(diào)控活性的dna片段。
Four colonies of transformed e . coli dh5 a with clear hydroiyzing zone on the chitin agar were obtained . the gene fragment in these isolates was identified by the methods of plasmid processing . dna sequencing analysis showed that sequence homology between pcr fragment and chromosomal dna of b . subtilis from 2599451 to 2812870 was 85 % , and was 30 % between the fragment and the genes encoding for chitinase of bacillus ( including b . subtilis ) in genebank
測(cè)序并序列比較結(jié)果表明該基因片段同已發(fā)表的枯草芽孢桿菌幾丁質(zhì)酶和內(nèi)切葡聚糖酶編碼幕因的克隆及重組芽抱桿菌的構(gòu)建glyb一apre之間的同源性是最高的，為35 % ;同bacz ’了了ussp . bp23ce1b 、 b . p朋刀us內(nèi)切葡聚糖酶和b . pol理vxap一1 ， 4一內(nèi)切葡聚糖酶的編碼基因的同源性只有27 % 。
Pcr amplification using 2 degenerate primers for nitrogenase fe protein gene was performed with chromosomal dna isolated from the 29 isolates . the result suggested that a nifh amplicon of 323 nucleotides was detected in 7 isolates and the 7 isolates are c4 c5 g1 g2 , w5 t1 and t7 . these pcr amplified fragments were cloned , and sequenced
首先利用芽孢桿菌中芽孢的抗熱性將土壤溶液在100沸水中煮10 - 15分鐘，然后用選擇性無(wú)氮培養(yǎng)基進(jìn)行初篩得到29株菌落形態(tài)不同的菌株；接著用固氮酶結(jié)構(gòu)基因nifh的特異性引物對(duì)這29株菌進(jìn)行pcr擴(kuò)增，結(jié)果表明其中7個(gè)菌株具有nifh基因，這7個(gè)菌株的編號(hào)依次為： c4 、 c5 、 g1 、 g2 、 w5 、 t1和t7 。
Strain pseudomonas psuedoalcaligenese ys1 was capable of producing phas containing monomer of hb and mcl has in certain medium . phacl and phac2 , two key polyhydroxyalkanoates polymerase genes of pha biosynthesis were amplified and cloned from chromosomal dna of pseudomonas psuedoalcaligenese ys1 using pcr
本研究利用聚合酶鏈?zhǔn)椒磻?yīng)( pcr )技術(shù)，從p . psuedoalcaligeneseys1染色體dna中擴(kuò)增并克隆了調(diào)控短鏈與中鏈pha生物合成的兩個(gè)關(guān)鍵酶基因： phac1 、 phac2基因。

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