接種培養基 的英文怎麼說

中文拼音 [jiēzhǒngpéiyǎngjī]
接種培養基 英文
inoculation medium
  • 接 : Ⅰ動詞1 （靠近;接觸） come into contact with; come close to 2 （連接; 使連接） connect; join; put ...
  • 種 : 種名詞（姓氏） a surname
  • 培 : 動詞1. （在根基部分堆上土） bank up with earth; earth up 2. （有目的地使成長、壯大） cultivate; foster; train
  • 養 : Ⅰ動詞1 （供養） support; provide for 2 （飼養; 培植） raise; keep; grow 3 （生育） give birth to ...
  • 接種 : [醫學] vaccinate; have an inoculation; inoculate
  1. Purpose : to explore the technique of induction of polyploidy in isatica indicago by colchicine treatment

    摘要採用直接浸漬和加入培養基法對菘藍種子進行誘導，探討秋水仙堿誘導菘藍多倍體的方法。
  2. Such a piece of transplanted tissue is called an explant, and its placement on the culture medium is called inoculation

    這種被移植的組織稱外植體，將它放置在培養基上稱為接種。
  3. Carefully mix the inoculum and the medium

    仔細混合接種物和培養基。
  4. Either instrument can be used to obtain the inoculum from an agar slant culture by carefully touching the surface of the solid medium in an area exhibiting growth so as not to gouge into the agar

    任何一種器具都可以用來在洋菜斜面培養上獲得接種原，小心地碰觸有生長的固體培養基的表面，避免刺破洋菜培養基。
  5. Here we studied the relationship of various factors and the quality of protoplasts. which maybe could be the basic of moss gene targeting. results showed : inoculated the spores onto diferrent kinds of media, such as ms, benecke and knop, we found that there was no difference when the spores germinated and differentiated into cauliform soon

    通過對立碗蘚的無菌培養和原生質體操作發現： （ 1 ）立碗蘚孢朔接種在無菌ms 、 benecke 、 knop培養基上，均可萌發產生原絲體，但不久便分化為莖葉體，很難長期保持其原絲體狀態，不同培養基條件下原絲體狀態有所不同。
  6. L. acidophilus strains pb1, a878 mixed with enterococcus strains m1, pb2, a30, a31. the amounts of cholesterol removed from growth medium were tesed after anaerobical incubation at 37 cthe amount of cholesterol assimilated higher 40 % by pb1 + m1, pb1 + pb2 a878 + a30, a878 + a31. the result indicated that pblmixed with ml, pb2 and a878 mixed with a30, a31 can assimilate cholesterol effectively

    將pb1 、 a878分別和各球菌m1 、 pb2 、 a30 、 a31接種于高膽固醇培養基中，在有膽汁和厭氧條件下， 37混合培養16 - 18h ，測定復合菌株和單菌株降低膽固醇的效果，以未接菌培養基為對照，結果表明， pb1與m1及pb2 ； a878與a30及a31的協同作用較好，降培養基中膽固醇的量都高於40以上。
  7. Water quality - enumeration of culturable micro - organisms - colony count by inoculation in a nutrient agar culture medium

    水質.可培養微生物的計數.營養瓊脂培養基中接種的計群法
  8. Water quality - enumeration of culturable micro - organisms - colony count by inoculation in a nutrient agar culture medium iso 6222 : 1999 ; german version en iso 6222 : 1999

    水質.可培養微生物的計數.用營養瓊脂培養基接種培養
  9. In this experiment, radio - immunoassay and hybridization in situ were applied to observe the insulinotropic activities of glp - 1 ( 7 - 36 ) nh2 and reveal the mechanisms underlying this process. methods : rat pancreases were removed from 3 - 5 day - old sprague - dawley rats and dissected into 0. 5mm3 segments and islets were isolated by the collagenase digestion method of wangling et al. thoroughly washed islets and suspended in modified rpmi - 1640 medium supplemented with 10 % fetal bovine serum, and added to 50ml cell culture flasks

    方法：胰島的分離參照王玲等的方法，每次實驗取新生3 - 5天sd大鼠，無菌條件下剖腹取出胰腺，剪切為0 . 5mm ~ 3的組織塊， v型膠原酶消化30min后，離心洗滌，懸浮於完全培養基，接種入50ml培養瓶，於5 co _ 2 、 95空氣條件下培養20h ，轉板純化，接種於96孔培養板培養24h ，按實驗要求進行實驗。
  10. Primary culture of rat preadipocyte were prepared from the epididymal, inguinal and perirenal the fat pads of male normal, healthy, 15 - 20 days sprague - dawley rats. the preadipocyte grew better under the condition of 37, 95 % humidity, 5 % co2, ph 7. 0 - 7. 2, centrifuged at 1000r / min, m199medium, and 10 % fetal bo vine serum, seeded at a density of 4 l04, 5 l04, / cm2. oil red o staining was the special method to distinguish adipocyte from other cells, gimsa and he could determine the stage of the adiopcyte differentiation through the number of lipid drop, size and the position of the nucleolus of the staining fat cell

    經過多次實驗，確定本實驗室大鼠前體脂肪細胞的最佳培養條件是：溫度為37 ，濕度為95 ， co _ 2濃度為5 ， ph值為7 . 0 7 . 2 ，離心力為1000r / min ，培養基為m _ （ 199 ）培養基，胎牛血清濃度為10 ，合適細胞接種密度為4 10 ~ 4 、 5 10 ~ 4個/ cm ~ 2 ，染色結果表明：油紅o染色是鑒定脂肪細胞的特異方法， gimsa和he染色可根據不同區域染色程度、著色差別判斷細胞核的位置及脂滴大小、多少，觀察大鼠前體脂肪細胞分化過程中的形態變化，進而確定脂肪細胞的分化階段。
  11. The results are as follows : exogenous hormones enhance hft gene expression. sequence alignment suggests hft ( hyacinthus forkhead transcription factor ) is a novel gene. its expressing level was enhanced by the hormones, and lower level were maintained in explants uncultured or cultured without hormones

    外源激素提高hft基因的表達水平， hft在外植體接種于含有生長素和細胞分裂素的ms培養基上培養24小時、 5天、 10天和15天的材料中均表達，並且其表達水平逐漸增高。
  12. This review includes the following subjects : induction frequency of haploids depend on genotypes, developmental stage of explants, temperature pretreatment of the explants, medium composition and the conditions of cultivation

    迄今己有9個科21種植物用這一方法誘導出單倍體植株，植物的基因型、外植體的發育程度、接種前的預處理、培養基和培養條件等均能影響誘導率的高低。
  13. Remember that after inoculation, petri dishes are incubated in an inverted position ( top down ) to prevent condensation that forms on the cover during solidification from dropping down onto the surface of the hardened agar

    記得在接種后，培養皿要倒著放，以避免在凝固時水氣凝集在蓋子上而滴入到硬化后的洋菜培養基表面。
  14. The results show that most isolates produce enough condia. which are similar to those directly received from the hosts, when they grow on the twa + w culture media for about 1 - 2 weeks, under 18 - 22 and alternative nuv light for 12h and in dark for 12h. but we should try several different kinds of culture media to produce the natural condia for some special species

    總結如下： （ 1 ）適宜培養基及適宜培養條件：使用自來水洋菜麥稈培養基（ twa + w ） ，近紫外燈照射下， 18 22下， 12h光照與12h黑暗交替培養時，大部分菌落生長較好；但對個別的種也應使用多種培養基，選擇最接近自然狀態的培養基和培養條件。
  15. The results of stem culture were as follow : b5 medium had faster bud germination and low browning. when subculture medium was b5 + ba2mg / l + naa0. 2mg / l, the numbers of propagation were 3. 2 times of explants, what ' s more, the seedlings were robust

    蝟實繼代培養基b _ 5 + ba2mg l + naa0 . 2mg l最為有利於蝟實芽的增殖，其芽的增殖數為接種數的3 . 2倍，小苗生長健壯。
  16. The methods of evans and martin were changed slightly and used to isolate the mouse es cell in my experiment. in brief, the intact blastocysts were plated on sto feeder layer treated with mitomycin, and were cultured in the media supplymented with brl condition medium

    聯合evans和martin的方法，稍加改良來分離小鼠胚胎幹細胞，把昆明白小鼠完整的囊胚直接種植在經絲裂黴素滅活的sto飼養層細胞上，在含有brl條件培養基的es細胞培養液中培養。
  17. After inoculation, all strains were examined by microscopy, hyphae or cells of all strains were observed, but none was seen in negative comparison. in the same time, originally fungi were isolated again in sabourud which showed that these fungi could grow and reproduce in these animals, but if they can cause infection or not will be make sure with impressionable animals

    回接后所有實驗菌種在顯微鏡下均可見有菌絲或菌細胞生長，而陰性對照組則未見生長，同時可以從沙堡氏培養基中再次分離得到該菌，說明這些菌種均可以在動物體內生長繁殖，但是否能真正引起感染，還需要進一步使用易感動物進行確認。
  18. For inoculation of an agar deep tube, a straight needle is inserted to the bottom of the tube in a straight line and rapidly withdrawn along the line of insertion

    在接種試管深層培養基時，一支直的接菌針直線地穿刺到試管的底部，同時快速地沿著接種線抽出。
  19. Tissue isolation of different positions of 9 matsutake were made with 8 media in 810 test tubes

    試驗採用8種培養基配方，對9個鬆口蘑子實體的不同部位進行組織分離，計接種試管810支。
  20. The sticky loop is then used to pick up a few seeds from the filter paper and to deposit them evenly across the agar surface

    已降溫的帶一定粘性的接種工具被用來取已經消毒的種子（或外植體）並將它們均勻地接在培養基上。
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