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- Citrus genomic DNA library was bloted with the AP1 and FBP1 mixed MADS box genes probe labeled by random primer method. 以大三島臍橙基因組DNA為材料 ,用擬南芥AP1和矮牽牛FBP1的混合質(zhì)粒DNA為模板 ,采用隨機引物法標記探針 ,對柑桔基因組DNA文庫進(jìn)行噬菌斑原位雜交。
- The particular band pattern of dark and light was observed by using random primer PRINS. 結果表明，隨機引物延伸在染色體上呈現明暗相間的帶紋樣特征。
- Citrus genomic DNA library was bloted with the AP1 and FBP1 mixed MADS-box genes probe labeled by random primer method. 以大三島臍橙基因組DNA為材料，用擬南芥AP1和矮牽牛FBP1的混合質(zhì)粒DNA為模板，采用隨機引物法標記探針，對柑桔基因組DNA文庫進(jìn)行噬菌斑原位雜交。
- Here we present the results of random primer and SOX degenerate primer PRINS on human metaphase chromosomes. 分別應用隨機引物和SOX基因兼并引物在人類(lèi)染色體上進(jìn)行了原位延伸標記。
- Methods: Optimal reaction system and single random primer of RAPD were used for genotyping of the 108 strains of EA isolated from the clinical samples and the genotype profile was drawn. 方法:以?xún)?yōu)化的反應體系和單一隨機引物對臨床分離的108株EA進(jìn)行RAPD法基因分型并繪制基因分型圖譜。
- random primer DNA labeling system 隨機引物DNA標記系統
- Results 20 random primers were screened out in total and one of which,the primer S1,was shown to accurately distinguish between Fritillaria hupehensis and Fritillaria unibracteata with very high specificity. 結果總共篩選了20條隨機引物,得到一條引物S1能準確區分湖北貝母、暗紫貝母,并且其特異性非常高。
- Analyzed the genome DNA of high-protein wheat of T4 and CK by 34 random primers using RAPD. 選用34個(gè)隨機引物對T4代高蛋白小麥和對照的基因組DNA進(jìn)行分析。
- In this experiment, differential expressing genes in leg muscle of chicken mentioned above were studied via DDRT-PCR technique, which firstly adopted 72 primer pairs that piloted by 3 T7 (dT11) N as anchor primers and 24 M13-ARPs as random primers. 本實(shí)驗采用3個(gè)26bp的T7(dT11)N為錨定引物,24個(gè)26bp的M13-ARPs為隨機引物,組成72個(gè)引物組合對上述四個(gè)品種雛雞腿肌組織進(jìn)行DDRT-PCR反應。
- Soiled dishes were piled at random. 臟碟子胡亂地堆放著(zhù)。
- The fingerprints amplification by polymerase chain reaction(PCR) with 6 polymorphic 10-based random primers selected from 40 ones was analyzed. 從40個(gè)引物(10堿基的寡核苷酸)中篩選出6個(gè)引物,對它們的PCR擴增結果進(jìn)行分析。
- The RNA was rerverse transcribed according to the illustration of cDNA first chain construction agent kit with random Primers Oligo dT. 由于其發(fā)病機理尚不完全清楚，早期診斷仍有困難。
- Total 67 random primers were selected in RAPD analysis.Sex differentiations of population level were found in 18 primers. 共篩選出67個(gè)RAPD隨機引物，其中18個(gè)引物擴增出了群體水平的性別差異。
- All of the 100 random primers screened for ISSR analysis gave clear amplification products, Twe of them amplified the polymorphic DNA in the NILs Thatcher and Lr37l6 Thatcher. 研究采用100個(gè)ISSR引物對小麥抗葉銹近等基因系進(jìn)行了分析，其中絕大多數引物能擴增出清晰可辨的條帶。
- Results showed that 189 DNA bands were amplfied with 22 random primers,of which 143 were polymorphic.An average proportion of polymorphic loci was 75. 66%. 結果顯示,22個(gè)引物共擴增出189條DNA條帶,其中143條表現出多態(tài)性,占總帶數的75．66%25。
- Abstract: 20 random primers,8 parental varieties and their 4 F1 of Hami-melon (Rock melon)(Cucumis subspecies.melo pang.)were analysed by RAPD technique. 文摘:利用20個(gè)隨機引物對厚皮甜瓜8個(gè)親本與4個(gè)雜交種進(jìn)行RAPD分析。
- I borrowed from the library a primer of phonetics. 我從圖書(shū)館借了一本語(yǔ)音學(xué)入門(mén)書(shū)。
- Methods: 8 primers were selected from 60 random primers to amplify the total DNA extracts of 17 samples with RAPD method and then the amplified were analyzed. 方法:從60個(gè)隨機引物中篩選出8個(gè)引物,采用隨機引物擴增多態(tài)DNA(RAPD)技術(shù),對8種卷柏屬植物的17份樣品的DNA提取物進(jìn)行擴增和分析。
- The genetic diversity among strains of chicken Shigella boydii, Shigella dysenteriae and S.Pullorum was studied by random amplified polymorphic DNA (RAPD) with 6 random primers. 摘要以雞鮑氏志賀菌、雞白痢沙門(mén)菌和痢疾志賀菌為研究對象，分別提取基因組DNA，利用6條隨機引物以隨機擴增多態(tài)性DNA(RAPD)技術(shù)對其基因組DNA進(jìn)行了分析。
- Differences were found among 8 strains from RAPD analysis.Out of 23 random primers, 11 were polymorphic.Altogether 59 RAPD bands were found and the polymorphic rate was 47.5%. 應用23個(gè)隨機引物對白粉病菌8個(gè)不同生理小種進(jìn)行RAPD分析，其中11個(gè)引物的擴增帶型在不同生理小種間出現差異，共擴增出59條譜帶，多態(tài)性為47.;5%25。
