gene type 中文意思是什麼

gene type 解釋
遺傳型
  • gene : n. 【生物學】基因。 dominant gene顯性基因。
  • type : n 1 型，類型，（工業產品的）品種；風格，型式。2 典型，榜樣，樣本，樣板，模範，範本；典型人物；具...
  1. Primary analysis of differential gene expression profile of type 1 and type 2 astrocytes

    兩型星形膠質細胞基因表達譜差異的初步觀察
  2. Twisting tongue was the recessive heredity of single gene of autosome, and the non - twisting type was the dominant character

    其中，尖舌、扣手和疊腿的遺傳方式為本文首次報道。
  3. The results showed as follows : ( 1 ) 6 traits are correlative with genomic factors according to analysis of population genetics and comparison of the coherence of twins. ( 2 ) the hereditary mode of rolling tongue or pointed tongue was the dominant heredity of single gene of autosome, and the can - rolling type or can - pointed type was the dominant character

    本文首次從群體遺傳學、家系分析、典型系譜分析及雙生子分析多個角度並結合多種相關數理統計方法，對6項人類學特徵的遺傳方式進行了探討，初步確定了各項特徵的遺傳方式，評價了各特徵的遺傳與環境的相對重要性。
  4. A four - gene block, a rwo - trna gene cluster and six single trna genes involved in the rearrangement, the second gene rearrangement type of mitochondrial dna reported for any pancrustacea arthropod. comparisons of mitochondrial gene arrangements of decapod suggested that rearrangement of the four gene - block found in eriocheir is informative for high level phylogenetic study of decapod

    發生重排的基因包括一個4基因塊的重排、 1個2基因的trna基因簇的重排和6個單一trna基因的重排，形成泛甲殼類線粒體dna的另一種基因重排類型。
  5. The results indicate that conserved motif glpl and cfly does not exist in ht gene, in other words, ht gene does not belong to the type of nbs - lrr resistance gene

    說明玉米ht基因不含絕大多數r基因特有的兩個保守序列glpl和cfly ，或者說ht基因不屬于nbs - lrr類r基因。
  6. All kind of oligonucleotides ( 16 sense primers, 8 antisenset primers, 128 different primer combinations in all ) were designed from the conserved motifs glpl and cfly ( distance between them is approximately 210bp ) which existed only in the type of nbs - lrr resistance gene and used as primers for scanning the genomic dna. no specific products ( which is approximately 210bp in length and obtained from genomic dna containing ht gene ) was obtained though amplified products of approximately 500 - looobp appeared in six different primer combinations

    依據nbs - lrr類r基因特有的兩個保守序列glpl和cfly （兩者相距約70個氨基酸）合成所有可能的簡並寡核苷酸引物（左引物16個，右引物8個，共組成128個引物組合）對玉米基因組dna進行擴增的結果表明：在6個引物組合中得到了擴增產物，產物長度在500 1000bp之間；沒有獲得特異性擴增產物（指僅從含ht基因材料中得到，長度約210bp的dna片斷） 。
  7. All f1 seedlings showed wild - type salt - sensibility, and two of four mutants were detected that the proportion of the salt - tolerance seedlings to salt - sensibility seedlings was 1 : 3 in f2 progenys. the results of genetic analysis suggested that this mutants have a monogenic recessive mutation in a nuclear gene

    F _ 1代白花授粉所得的f _ 2代中，兩個株系抗鹽植株與不抗鹽植株的比例為1 ： 3 ，表明該突變體是隱性單基因突變體。
  8. This method can be widely applied in type ii pha synthase gene cloning

    該方法的特點是簡單易行、重復性好且適用性強。
  9. The result showed that the homology rate of pila gene among the 5 avian pathogenic e. coli strains tested and one human e. coli were from 89. 8 % to 91. 1 %, and the homology rate of amino acid were from 88. 5 % to 91. 8 %. the homology rate of pila gene sequence among 5 avian pathogenic e. coli strains tested and avian pathogenic e. coli reported ( serotype o1, o2, o78 ) were from 87. 8 % to 90. 2 %, and the homology rate of amino acid were from 84. 6 % to 91. 2 %. there had homology in avian pathogenic e. coli. there had some common antigen side in type 1 pili of avian pathogenic e. coli

    結果表明：運用msha法檢測1型菌毛的檢出率為80 （ 36 45 ） ， pcr法的檢出率為95 . 5 （ 43 45 ） ， pcr方法用於1型菌毛的檢測比msha更加敏感、快速、特異性強；選擇5株優勢血清型雞源致病性大腸桿菌代表株（ o _ （ 89 ） ， o _ （ 119 ） ， o _ （ 141 ） ， o _ （ 127 ） ）的1型菌毛pila基因的pcr擴增片段經純化后，分別定向克隆到puc18質粒的多克隆位點，構建了含有目的基因片段的克隆質粒，並轉化到dh5株大腸桿菌載體菌中，篩選獲得陽性克隆菌株。
  10. In this paper, 45 e. coli strains isolated from chicken farms in sichuan province were determined to be the pathogenic e. coli by animal test. type 1 pili of 45 strains isolated was detected by msha. the pila gene of 45 avian pathogenic e. coli strains were amplified by the polymerase chain reaction ( pcr ) with primers designed according to the sequence of the pila gene in genbank. results showed that pcr was more sensitive, faster and more characteristic than msha to detect type 1 pili

    本研究將從四川規模化雞場分離鑒定、經1日齡雛雞致病性試驗得到的雞源致病性大腸桿菌45株，採用d -甘露糖敏感血凝試驗（ msha ）檢測1型菌毛，根據genbank中公布的人源大腸桿菌1型菌毛pila基因序列設計一對引物用pcr擴增雞源致病性大腸桿菌1型菌毛pila基因。
  11. This suggested that there was a match relationship between the c / y gene type and serotype of the host. 2

    對4 . 4kb片段進行了部分序列分析，繪出了基因上游650bp序列的精確酶譜。
  12. Ddrt - pcr method was exploited to study the differential gene expression between immature siliques of arabidopsis wide - type and ast mutant

    採用ddrt - pcr的策略，分析野生型與突變型植株未成熟角果中基因表達的差異。
  13. Detection of a new virulence associated gene in streptococcus suis type 2 jiangsu isolate

    雞生長軸相關基因的研究進展
  14. Wild type gene

    野生型基因
  15. Isolation and gene type detection of wild - type measles viruses in shaanxi province

    陜西省麻疹野病毒的分離及基因分型
  16. The kind of the y. pestis out membrane protein and the application of gene type in china

    中國鼠疫菌外膜蛋白種類及在基因分型中的應用
  17. In the sediment, bacteria belonging to the cfb ( cytophaga - flexibacter - bacterioides ) group and the - proteobacteria, - proteobacteria were the main groups. the 16s rdna diversity of 7th layer was different from that of other layers, including the analysis of rflp, gene type and the population of cfb group. and the population of - proteobacteria showed inverse ratio with that of cfb group

    基於以上的試驗，我們分析了企鵝糞便沉積物中微生物生態與環境變化和環境污染的關系並提出了沉積物中出現的異常在環境和氣候方面可能的解釋，初步建立了以分析企鵝糞便沉積物中微生物多樣性為手段的新的考察南極氣候變遷和環境污染的思路。
  18. Furthmore, on the higher coefficient level, the individuals in each group are sorted into subgroups. by the selected amplification results with one pair of primer, the wild germplsms were efficiency distinguished. the traditional classification of cavendish subgroup based on caudex height is not strict corresponded with gene type similarity

    在相似系數0 . 62的水平上將供試的60份蕉類植物分為四個群體，在相似系數0 . 64的水平上將栽培蕉劃為兩個類群，在相似系數0 . 83的水平上將香牙蕉類群劃分為五個亞群；用一對引物的aflp分析對25個野生蕉進行了劃分；認為傳統的將cavendish亞群分為五個類別的分類依據與基因型之間並無嚴格的對應關系。
  19. Gene type of tomato was another important factor affected its fst

    基因型也是影響番茄座果率的一個重要因子。
  20. The strains of gene type 1 contain crylaa, crylac, cry2, crylc and cryld gene and the strains of type 2 contain crylaa, cry2, crylc and cryld

    基因類型1含cry1aa和cry1ac ，基因類型2含cry1aa 。這一結果為基因工程菌的構建提供了理論依據。
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