雜交株 的英文怎麼說

中文拼音 [jiāozhū]
雜交株 英文
hybrid strain
  • : Ⅰ形容詞(多種多樣的; 混雜的) miscellaneous; varied; sundry; mixed Ⅱ動詞(混合在一起; 攙雜) mix; blend; mingle
  • : Ⅰ動詞1 (把事物轉移給有關方面) hand over; give up; deliver 2 (到某一時辰或季節) reach (a cert...
  • : Ⅰ名詞1. (露在地面上樹木的根和莖) root and stem of a tree above the ground 2. (植株) individual plant; plant Ⅱ量詞(棵)
  • 雜交 : [生物學] hybridize; cross; hybridization; cross breeding
  1. It was suggested that eric - pcr could substitute for rapd in research related to the genetic identification and genetic diversity in auricularia and other edible and medicinal fungi : 2 to a certain extent, genetic differences among auricularia strains tested in this study did not have necessary relativity with their geographical origins respectively ; 3 in this study, genetic diversity in a. polytricha was higher than that in a. auricula : 4 in this study, a. fuscosuccinea had a higher homology to a. auricula than to a. polytricha ; 5 morphological characteristics validated the results from eric - pcr and provided a potential explanation for the higher similarity coefficient between a. auricular and a. fuscosuccinea ; 6 southern hybridization was employed by choosing a strain from a. auricula as a probe which hybridized with a. auricula and a. fuscosuccinea except a. polytricha, further confirming the veracity of the results from eric - pcr ; 7 in this study, isozyme analysis could not cluster the 7 strains from three auricularia species to different groups efficiently ; 8 2 strains from two auricularia species revealed high conservative degree and the restriction fragment patterns by 4 kinds of restricted enzymes showed no diversity

    本研究中,木耳屬2個種的2個菌在its區域表現出較高的保守性, 4種限制型內切酶的酶切圖譜沒有顯示出多態性;增加內切酶種類及供試菌數量,有可能獲得具有多態性的限制性內切酶酶切圖譜; 9本實驗中, its區域的真菌特異性引物與真核生物通用引物對于擴增效果無較大差異,擴增片段長度均為650bp左右; 10根據形態學實驗、 eric - pcr實驗以及southern實驗的結果分析,紫木木耳屬種質資源的遺傳鑒定和遺傳多樣性評價耳極有可能是毛木耳種的一個變種; n .本研究中所用的gutc法是一種適用於木耳屬菌基因組洲a快速提取的方法; 12 .傳統的形態學分類法和現代的分子生物學分類法,兩者的關系是相輔相成,互為驗證
  2. ( 2 ) gene flow frequency was reduced as distance from pollen donor increased and a dramatic reduction occurred at about 2 meters. the maximum distance where gene flow was not detected was 50 m for hybrid rice while it was 70 m for ms lines, with an exception that in one of the four ms lines it was detected a frequency of gene flow 2. 8 + 10 - 6 at 150 m for zhong 9a

    在開花期主流風向ne的風速為0 . 2 ? 2 . 2m / sec的條件下, 2個稻品種的最大漂流距離為40m ; 4個不育系的基因漂流基本上到60m為止, 70m處基因漂流頻率均降為0 ,僅中9a在150m處發現了1basta抗性苗,經pcr檢測驗證為陽性。
  3. Embryo culture and plant regeneration from cotyledons in interspecies hybrids of cherry

    櫻桃種間種胚培養及子葉植再生
  4. Double cross - over strains aved24 and avec9 were obtained after growth of several generations on mym plate with or without antibiotics selection. genomic dna of double cross - over strains aved24 and avec9 were extracted and southern hybridization were performed

    分別提取同源雙換茵aved24和avec9基因組dna ,通過薩瑟恩( southern ) dna印跡,結果證明l
  5. Shaking flask experiments and hplc analyses showed that the four mutants no longer produced the toxic oligomycin, and only made four components of avermectins b, which were avermectin b1a, b1b, b2a, b2b. the yields of avermectins b in these mutants were separately equal to those in cz8 - 73. this revealed that olma genes deletion did n ' t affect the biosynthesis of avermectins

    將4經southern驗證正確的基因缺失突變進行搖瓶發酵和hplc檢測,發現4個突變均不再產生寡黴素而僅產阿維菌素b組分,阿維菌素的總產量和b1的產量與出發菌相當,說明寡黴素pks基因簇的缺失並不影響阿維菌素的生物合成。
  6. 2 - e4 and s2 is induced respectively by 8 - ag and 5 - brdu with different drug concentration to make them deficient in hypoxanthine - guanine phosphoribosyl transferase ( hgprt ) and in thymidine kinase ( tk ) respectively and renamed 2 - e4 - a and 82 - 6. their antibodies " isotypes are tested by goad anti - mouse isotype regent

    取馴化好並處于對數生長期的2 - e _ 4 - a和s _ 2 - b細胞,再常規融合和篩選,三次克隆化后得穩定分泌雙特異性抗體的-瘤細胞6
  7. Protoplasted monokapyon ( pm ) were prepared from lentinus edodes strains jingxuan and wuxiang, respectively, intercross process were put in practice

    摘要以香菇菌精選和武香作為親本制備單核原生質體,將兩個親本的單核原生質體進行一一
  8. Abstract : the main characters and seed set of bc1 , bc2 , bc1f2 from ms line back - crossing with the pollen of hybrid rice were studied. the appearance of a large number of self fertile plants in ms line was analyzed. the effect of introgression of restoring genes on ms line purity and hybrid yield in indica and japonica rice was discussed. it was pointed out that “ iso - cytoplasm restorer line ” was seriously reducing the purity of ms line and that hybrid rice was unsuitable for isolation zone in the seed production fields

    文摘:研究了稻花粉對母本不育系回後代群體bc1 、 bc2 、 bc1f2的主要農藝性狀和育性表現,分析了不育系中出現大量自結實的原因,討論了恢復基因滲入對秈、粳不育系純度和稻產量的影響,指出「同質恢」對降低不育系純度的嚴重性和稻作制種田隔離區的不合理性。
  9. The ascites fliud titer of the other hybridoma s2 for further hybridization is 1 : 16000 by blood agglutination. the isotype of 2 - e4 is igg2a, and s2 is iggs

    用於再的另一細胞為本室保存的分泌抗人a型紅細胞單克隆抗體的瘤細胞s ; ,其血凝效價為l : 16000 。
  10. Guan xiaohong ( 1991 ) established a cell line of the monoclonal anti - idiotypic antibody ( anti - id ) np30 of schistosoma - 6 - japonicum, whose isotype was identified to be igm and which was testified to be internal image of gaa

    分別以日本血吸蟲單克隆抗獨特型抗體wbo的瘤細胞總基因組dna和其提取rna進行rticr合成的cdna第一鏈為模板,擴增v 。 、 v 。
  11. Preparation and characterization of monoclonal antibody against botulinum neurotoxin type b

    型肉毒毒素單克隆抗體的建立
  12. Serious cross reation existed between v. albo - atrum and mv2, mv3, mv4. the other pathogen isolates v31 and v32 also had cross reactions, but the reaction was not serious. because limited number of pathogen isolates were selected, it could not prove that the selected immunogen was widely presentative, more pathogens isolates should be tested to verify the acquired hybridomas cells

    5單抗瘤細胞中沒有一具有種或屬的特異性,其中mv2在棉花黃萎病菌若干菌系間的檢測表明其能夠區分不同的致病類型; mv1和mv4組合檢測的結果基本上能將棉花大麗輪枝菌鑒定到種;黑白輪枝菌與mv2 , mv3 , mv4的叉反應比較強烈,其他菌v3 , v32有個別的叉反應,但不強烈
  13. Frankfurt os, robb ja, sugar baker ev, et al. monoclonal antibody tosingle2stranded dna is specific and sensitive cellular marker of apoptosis [ j. exp cell res, 1996, 226 ( 2 ) : 3872397

    吳國慶,李少華,徐志偉,等.抗單鏈單克隆抗體瘤細胞的建立及鑒定[ j ] .細胞與分子免疫學志, 2002 , 18 ( 5 ) : 4792480
  14. Sds - page results showed that there was a clear target protein band in mut + recombinant supernatant after 48 hours of culturing, while a faint band only in muts recombinant after 72 hours. western - blotting result showed that there was no remarkable difference of yield between mut + and muts recombinants after 6 days induced. anti - virus activity tests revealed that culture supernatants of mut + and muts recombinants could inhibit tmv infection with high efficiency in the same concentration and there was no significant difference between them

    結果表明,誘導培養48小時后, mut ~ +重組菌表達產物在sds - page膠上顯現出清晰的目的蛋白帶,而mut ~ s重組菌培養72小時才能顯示微弱的目的帶; western - blotting信號強度表明,同樣培養6天的mut ~ +和mut ~ s重組菌表達產物在表達量上沒有明顯差別。
  15. To dress the question if other virulence gene were present in this kind of strains, 152 of 436 irp2 - hybridized strains were re - confirmed and selected for this study. the virulence genes or putative virulence genes detected by pcr or hybridization include heat stable toxin ( st ) & heat labile toxin ( lt ) for enterotoxigenic e. coli ( etec ), invasive plasmid antigen b ( ipab ) for enteroinvasive e. coli ( eiec ), epec adherence factor ( eaf ), epec secretion protein c ( espc ) for enteropathogenic e. coli ( epec ), hemolysin ( hlya ) and shiga toxins ( sltl and slt2 ) for enterohaemorrhagic e. coli ( ehec ) and eaggec probe for entero - aggregative e. coli ( eaggec ). the prra and yc73 genes of pathogenicity associated island ( pai ) of urepathogenic e. coli ( upec ) and " o " island 28 ( rtx 615 ) gene was also detected, the later was a newly discovered putative pathogenicity island in e. coli o157 : h7

    為探討攜帶小腸結腸炎耶爾森氏菌的hpi毒力島的大腸桿菌是否具有其他已知的毒力基因,選取82由原位和pcr方法初篩irp2陽性的大腸桿菌菌,進行在致瀉性大腸桿菌的25個毒力基因的檢測,包括腸產毒性大腸桿菌的熱穩定毒素st和熱不穩定毒素lt ,腸侵襲性大腸桿菌的侵襲蛋白b基因ipab ,腸致病性大腸桿菌的eaf 、 espc基因,腸出血性大腸桿菌的溶血素hly 、志賀毒素1 ( slt1 ) 、志賀毒素2 ( slt2 )基因,腸集聚性大腸桿菌的eaggec探針,以及在泌尿道致病性大腸桿菌和o157 : h7大腸桿菌中新發現的毒力島基因。
  16. The space distribution of pigment gland density on eleven places was analyzed by allotetraploid of ( g. arboreum g. bickii ) and varieties with pigment gland of g. hirsutum g. barbadense and the progeny population which is crossed by allotetraploid of ( g. arboreum g. bickii ) g. hirsutum and ( g. arboreum g. bickii ) g. barbadense

    摘要利用(亞洲棉比克氏棉)異源四倍體和陸地棉、海島棉有色素腺體品種以及由(亞洲棉比克氏棉)異源四倍體為母本,以陸地棉和海島棉有色素腺體品種為父本,組配成的後代群體,對植上十一個部位色素腺體密度在群體內的分佈進行了初步分析。
  17. The authors discovered four peculiar phenomena, i. e., the self seed - setting and its genetic stability of the autoteraploid rice, the early - generation stabilization in the cites between alloploid rices, the self embryogenesis of autoteraploid rice wider isolated conditions, and a high seed - setting percentage in some plants of autotetraploid rice after the treatment of ion beam, in the research of autotriploid and autotetraploid rices

    在對同源三倍體水稻和同源四倍體水稻的研究中發現了值得注意的4種奇特現象,即同源三倍體水稻的結籽現象及其倍性的遺傳穩定性、在異倍性水稻間的後代中早世代性狀穩定遺傳的現象、在隔離條件下同源四倍體的胚自發現象和離子束注入后同源四倍體水稻單的高結實現象。
  18. Molecular examination and biological observation of transformed plants by growing resistant germinations we got 30 transformed plants. pcr and spot blotting hybridization analysis indicate that hsp70 anti - sense cdna had been integrated into tobacco genome. through observation and measurement we found 12 completely sterile, 9hyper - sterile, 3 partially sterile and 6 fertile and significant differences between them in stamen, height, and fruit weight

    Pcr和點分析表明, hsp70正、反義。 dna己經整合到煙草的基因組中。在進行田間生物學性狀觀察時, 30轉基因植中有12表現出完全不育, 9高度不育, 3部分不育和6可育;不育植在雄蕊、高和果實重量等方面都存在明顯的差異。
  19. So streptomyces sp. fr - 008 is a new strain synthesizing candicidin. nmr studies analysis of the 1h - 1h cosy spectrum allowed us to distinguish some important chemical shifts of the protons in fr - 008b which could be identified as eandicidin d. especially for amino - mycosamine residue, methyl protons and all the protons on the ring could be defined by correlating relation

    利用與糖基合成有關的基因str - de作探針對這兩個菌的總dna進行了southern,從兩個菌的總dna中均檢測到一段相同大小的陽性片斷,約6 . 4kd ( bamhi + bglii酶切) 。
  20. 2 - e4 - a and 82 - 6 are hybridized during their log growing time, and the hybrid - hybridomas are cloned for 3 times and produce 6 hybrid - hybridoma cells. the chromatosome of hybrid - hybridoma 3 - hu and hybridoma 2 - e4 - a and s2 - b are counted, and the antibody of ascites fluid or culture supernatant of 3 - hn is prepared. the positive clones are detected by three methods at the same time : rbc agglutination for monospecific anti - human rbc type a antibody, indirect elisa for anti - p24 antibody, and rbc solid - phase adherence for bispecific antibody

    選其中一3 - h _ ( 11 )做-瘤細胞染色體計數,同時計數兩母2 - e _ 4 - a和s _ 2 - b的染色體數:制備腹水型和上清型抗體,用三種方法同時檢測其中的雙特異性抗體、單特異性抗人紅細胞抗體和抗p24抗體,即紅細胞固相吸附法測雙特異中文摘要性抗體,紅細胞凝集試驗測單特異性抗人a型紅細胞抗體,間接elisa法測抗p24抗體;用腹水型抗體做耐熱性及耐凍融實驗。
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