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susceptible bulk
相关语句
  感病池
     【Result】An AFLP primer pair,E20M64,was polymorphic between the resistant and susceptible bulk at 130bp.
     【结果】AFLP引物组合E20M64在抗病池和感病池间约130 bp处表现多态性。
短句来源
     To identify scab resistant genes, the F_2 population and the recombinant inbred line (RIL) population developed from the crossing of two wheat cultivars Wangshuibai and Nanda2419 were evaluated for scab resistance. A resistant bulk and a susceptible bulk were prepared according to the F_2 resistance evaluation data and screened for candidate markers associated with scab resistance with randomly amplified polymorphic DNA markers (RAPD).
     为了发掘抗赤霉病基因,对小麦品种望水白×南大2419的F2群体及其重组自交系群体进行了赤霉病表型鉴定,并根据F2抗性表型分别配制抗病池和感病池,用RAPD方法筛选与抗赤霉病基因连锁的候选标记。
短句来源
  “susceptible bulk”译为未确定词的双语例句
     With a F2 population derived from 66 ×A18 as materials,polymorphism between resistant and susceptible bulk of cucumber anthracnose were studied using BSA method and AFLP technology. A codominant AFLP marker,E24M48-251 bp/245 bp,was screened.
     以黄瓜抗炭疽病母本66和感炭疽病父本A18及其F2代分离群体为试材,采用BSA法和AFLP技术建立了对炭疽病的抗病组和感病组,AFLP引物组合E24M48在抗感组间表现多态性,且呈共显性。
短句来源
     DNA fragment OPN11 980 was amplified in resistant parent 95 5383 and resistant bulk, OPN11 1070 was amplified in susceptible parent HB1 and susceptible bulk.
     利用BSA法对 95 - 5 383× HB1的 F2 代进行鉴定 ,筛选出 RAPD引物 OPN11在 95 - 5 383和抗池扩增出 OPN11980 片段 ,在HB1和感池扩增出 OPN111 0 70 片段 ,在 F1 同时扩增出 OPN11980 和 OPN111 0 70 。
短句来源
     Results showed that a protein P40 (pI 6.3, Mw 40 kD) was significantly reduced or vanished after BPH infestation for 48 h in the susceptible bulk, while it remained uninfluenced in the resistant bulk.
     结果发现 ,虫害 48h后 ,感虫集团的一个分子量为 40kD的蛋白质P40 (pI=6 .3)的表达明显减弱甚至消失 ,而在抗虫集团中 ,P40的表达未受影响。
短句来源
     The random amplified polymorphic DNA (RAPD) analysis was made to identify polymorphic markers between resistant bulk and susceptible bulk DNA with 300 random primers.
     使用 30 0个随机引物进行 RAPD检测 ,发现引物 OPG0 9可在抗感性 DNA池之间产生 96 0 bp的稳定的相斥型多态性产物。
短句来源
     With a F2 population between a highly resistant parent and a highly susceptible parent (Q9 × Q10) as materials, polymorphism between resistant and susceptible bulk of cucumber powdery mildew were studied using BSA method and AFLP technology. A co-dominant AFLP marker, P18M47 -238 bp/236 bp, was screened.
     以黄瓜抗白粉病母本Q9和感白粉病父本Q10及组合(津春3号)的F2分离群体为试材,采用BSA法建立了对白粉病的抗病组和感病组,AFLP引物组合P18M47在两组间表现多态,且呈共显性。
短句来源
  相似匹配句对
     They are susceptible to Propoxur.
     对残杀威尚处敏感水平 ;
短句来源
     bulk compound semiconductors;
     体化合物半导体;
短句来源
     but susceptible to vancomycin.
     对万古霉素敏感。
短句来源
     Bulk Amorphous Alloys
     大体积非晶态合金材料
短句来源
     【Result】An AFLP primer pair,E20M64,was polymorphic between the resistant and susceptible bulk at 130bp.
     【结果】AFLP引物组合E20M64在抗病池和感病池间约130 bp处表现多态性。
短句来源
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  susceptible bulk
Of the 19 co-dominant markers, one primer,OPA16, amplified a resistant parental band in the resistant bulk and asusceptible parental band in the susceptible bulk by bulked segregantanalysis.
      


One SMV resistant soybean line(95 5383) was crossed with four susceptible soybean varieties/line(HB1, Tiefeng21, Amsoy, Williams) and one resistant variety PI486355. Their F 1 and F 2 individuals were identified for SMV resistance by inoculation with SMV3. The results showed that in the four crosses of resistant×susceptible, F 1 were susceptible and the ratio of F 2 populations was 1 resistant∶3 susceptible (mosaic and necrosis), indicating that 95 5383 carries one recessive gene that confer resistance...

One SMV resistant soybean line(95 5383) was crossed with four susceptible soybean varieties/line(HB1, Tiefeng21, Amsoy, Williams) and one resistant variety PI486355. Their F 1 and F 2 individuals were identified for SMV resistance by inoculation with SMV3. The results showed that in the four crosses of resistant×susceptible, F 1 were susceptible and the ratio of F 2 populations was 1 resistant∶3 susceptible (mosaic and necrosis), indicating that 95 5383 carries one recessive gene that confer resistance to SMV. There is a segregation of susceptibility in F 2 progenies from the cross of 95 5383×PI486355, indicating that the SMV resistance genes in 95 5383 and PI486355 are located at different loci. By bulked segregant analysis(BSA) in F 2 populations of 95 5383×HB1, one codominant RAPD marker OPN11 980 /1070 closely linked to SMV resistance gene amplified with RAPD primer OPN11 was identified. DNA fragment OPN11 980 was amplified in resistant parent 95 5383 and resistant bulk, OPN11 1070 was amplified in susceptible parent HB1 and susceptible bulk. OPN11 980/1070 was amplified in F 1. Identification of the markers in F 2 plants showed that the codominant marker OPN11 980/1070 is closely linked to the SMV resistance gene in 95 5383, with genetic distance of 2.1cM.

利用高抗东北 SMV3号株系的大豆品系 95 - 5 383与 4个感病品种 (系 ) HB1、铁丰 2 1、Am soy、William s和抗病品种 PI486 35 5配制 5个杂交组合 ,对各组合的 F1 、F2 代接种 SMV鉴定抗性。结果表明 ,95 - 5 383与各感病品种杂交组合的 F1 代表现为感病 ,F2 群体分离比例为 3感 (花叶 +顶枯 )∶ 1抗 ,表明 95 - 5 383对 SMV3号株系的抗性受一对隐性基因控制。 95 - 5 383× PI486 35 5的 F2 代接种后有感病植株分离 ,表明二者对 SMV3的抗性基因不等位。利用BSA法对 95 - 5 383× HB1的 F2 代进行鉴定 ,筛选出 RAPD引物 OPN11在 95 - 5 383和抗池扩增出 OPN11980 片段 ,在HB1和感池扩增出 OPN111 0 70 片段 ,在 F1 同时扩增出 OPN11980 和 OPN111 0 70 。用该引物分析 95 - 5 383× HB1的 F2 个体 ,共显性的 RAPD标记 OPN11980 /1 0 70 与 95 - 5 383抗病基因的遗传距离...

利用高抗东北 SMV3号株系的大豆品系 95 - 5 383与 4个感病品种 (系 ) HB1、铁丰 2 1、Am soy、William s和抗病品种 PI486 35 5配制 5个杂交组合 ,对各组合的 F1 、F2 代接种 SMV鉴定抗性。结果表明 ,95 - 5 383与各感病品种杂交组合的 F1 代表现为感病 ,F2 群体分离比例为 3感 (花叶 +顶枯 )∶ 1抗 ,表明 95 - 5 383对 SMV3号株系的抗性受一对隐性基因控制。 95 - 5 383× PI486 35 5的 F2 代接种后有感病植株分离 ,表明二者对 SMV3的抗性基因不等位。利用BSA法对 95 - 5 383× HB1的 F2 代进行鉴定 ,筛选出 RAPD引物 OPN11在 95 - 5 383和抗池扩增出 OPN11980 片段 ,在HB1和感池扩增出 OPN111 0 70 片段 ,在 F1 同时扩增出 OPN11980 和 OPN111 0 70 。用该引物分析 95 - 5 383× HB1的 F2 个体 ,共显性的 RAPD标记 OPN11980 /1 0 70 与 95 - 5 383抗病基因的遗传距离为 2 .1c M。

DNA markers linked to resistance locus of Marssonina leaf spot in poplars were found by bulked segregant analysis (BS A). The bulks consisted of individual with a extreme phenotype taken from a population of 91 Fj clones, which is a progeny of Populus deltoides Bartr. cv. "Lux"(I-69/55) (Resistance) and P. euramericana cv. I-45(Susceptible). Out of 114 RAPD primers,four markers showed polymorphisms between the resistance-bulk and the susceptible-bulk. By using selective genotype linkage...

DNA markers linked to resistance locus of Marssonina leaf spot in poplars were found by bulked segregant analysis (BS A). The bulks consisted of individual with a extreme phenotype taken from a population of 91 Fj clones, which is a progeny of Populus deltoides Bartr. cv. "Lux"(I-69/55) (Resistance) and P. euramericana cv. I-45(Susceptible). Out of 114 RAPD primers,four markers showed polymorphisms between the resistance-bulk and the susceptible-bulk. By using selective genotype linkage analysis, OP All 7 -1550 and OPAI13 - 900 were found linked to the resistance locus. The genetic distances between the two markers and the resistance locus were 29. 9cM and 37. 4cM,respectively.

以美洲黑杨(Populus deltoides Bartr.cv.“Lux”:I-69/55))为母本,欧美杨(P.euramericana cv.I-45)为父本得到的F1为材料,其中I-69对黑斑病表现为高度抗病,I-45为高度感病。利用分离群体混合分析(bulkedsegregrants analysis,BSA)技术建立两个DNA池(感病池和抗病池),筛选出了与抗黑斑病性状基因相连锁的RAPD标记:OPAI17-1550、OPAI13-900。利用选择性基因型分析法进行标记-抗黑斑病基因连锁分析,两标记与抗黑斑病基因遗传距离分别为29.9cM和37.4cM。

A highly resistant primitive cultivated species Solanum phureja was employed to generate a mapping population to perform the bulked segregant analysis (BSA) for screening and study of RAPD markers linked to the potato resistance to bacterial wilt. The random amplified polymorphic DNA (RAPD) analysis was made to identify polymorphic markers between resistant bulk and susceptible bulk DNA with 300 random primers. Primer OPG09 produced a 960 bp reproducible band only in the resistant clones, linking to...

A highly resistant primitive cultivated species Solanum phureja was employed to generate a mapping population to perform the bulked segregant analysis (BSA) for screening and study of RAPD markers linked to the potato resistance to bacterial wilt. The random amplified polymorphic DNA (RAPD) analysis was made to identify polymorphic markers between resistant bulk and susceptible bulk DNA with 300 random primers. Primer OPG09 produced a 960 bp reproducible band only in the resistant clones, linking to the resistance in the population. The marker was successfully used in examination of another population with similar genetic background.

用原始栽培种 Solanum phureja作为抗源构建了一个二倍体马铃薯作图群体 ,并且用于进行群分法 (bulked segregant analysis,BSA)分析 ,以筛选检定马铃薯青枯病抗性的 RAPD连锁标记。使用 30 0个随机引物进行 RAPD检测 ,发现引物 OPG0 9可在抗感性 DNA池之间产生 96 0 bp的稳定的相斥型多态性产物。进一步分析分离群体并得到与抗性相连锁的标记 OPG0 9960 。该标记已有效地应用于检测其它具相近遗传背景的二倍体群体的抗性

 
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