agar medium 中文意思是什麼
agar medium
解釋
瓊脂培養基-
The virulent strains had a polysaccharide capsule and formed smooth colonies on agar medium.
有毒菌株具有多糖莢膜它在瓊脂培養基上形成光滑的菌落。 -
The study aimed to establish a simple, inexpensive, nearly - maintenanceless and flexible hydroponic system for growing arabidopsis thaliana plants by combining agar medium plus ms nutrients with the eppendorf tube system
根據擬南芥的生長需求特點，採用ms培養基與營養液培養相結合的方法建立了一種簡單、低耗、低維護和靈活的擬南芥植株水培系統。 -
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。 -
Cut agar agar into small pieces, soak in the other half of water. boil with medium heat, stir constantly. remove from heat when agar agar is totally dissolved
瓊脂剪成碎片，泡入到餘下的冷水中，用中火煮沸，多多攪拌，到瓊脂完全融解后熄火。 -
The positive colonies that grew on the ampicillin ( amp ) plate ( lb agar medium contaning 100 g / ml amp ) were screened and identified. sds - page and western blot analysis were performed to study the expression profiles of target gene cein in e. coli
從轉化的平板中篩選出陽性重組子，進行不同iptg濃度和不同誘導時間的表達研究，並利用sds - page電泳和westernblotting蛋白質印跡技術對外源基因cei _ （ 12 ）在大腸桿菌e -
Water quality - enumeration of culturable micro - organisms - colony count by inoculation in ? nutrient agar culture medium
水質.可培養微生物的計數.培養營養瓊脂培養基計群法 -
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 -
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 -
It was found that b - 6 isolated by the method of distinct zone of clearing in cellulose - congo red agar medium combined with measuring the enzyme activity of liquid culture filtrates had comparatively higher cellulase activity. by measuring activity of cellulase of strains growing in medium with different carbon sources and of washed mycelium induced by different carbon sources in certain time, it found that the formation of cellulase was regulated by the nature of the carbon source used for b - 6 and as3. 3711
真菌纖維素酶是一種誘導酶，碳源同時也是主要的誘導物來源，為了研究碳源對真菌纖維素酶合成的誘導機理，本文利用液體生長培養和洗滌菌絲誘導培養法研究了不同碳源對兩菌株的誘導特性，並用電泳分析法研究了不同碳源的誘導酶譜。 -
Potato dextrose agar and grain medium were also used to identify fungi which were not determined by the primary culture. fungi were all secondarily cultured on sabouraud medium to observe the colony ' s texture, colour, growth rate, surface status and reverse pigment. the fungi should be examined by microscope to inspect their microscopic structure from 7th day to 21st day
使用的培養基有沙氏培養基、土豆培養基、真菌試驗培養基和5種種子培養基，連續培養4周，並隨時觀察菌落的色彩、生長速度、表面狀態、背面顏色等，並從第7天?第21天連續鏡檢以檢查真菌的顯微結構，綜合菌落形態和顯微結構，以確定真菌的種屬。 -
Many researchers have conducted experimellts about it, but not succeeded. culture media were compared to find the best medium of gingkgo culture for controlling callus browning by different sugars, antioxidants and sorbents. the result showed that the medium with ms + zt 1. 0mg / l + naa 1. 0mg / l + sucrose 50g / l + agar 8g / l + ac 2g / l was the best medium, at l5 days subculturing intervals
銀杏組織培養過程中，尤其是在愈傷組織的繼代培養中，褐變現象特別嚴重，曾有不少的人做過這方面的研究，但都沒有成功，而本研究通過對不同糖類物質、抗氧化劑、吸附劑以及不同的培養基對褐變的影響和控制效果，探索出有效控制褐化現象發生的最佳培養條件，試驗結果表明： ms + zt1 . 0mg / l + naa1 . 0mg / l +蔗糖50g / l +瓊脂8g / l + ac2g / l培養基上的繼代效果最好，繼代時間最好在15d左右。 -
Culture medium a mixture of nutrients used, in liquid form or solidified with agar, to cultivate microorganisms, such as bacteria or fungi, or to support tissue cultures
培養基：以液體或添加瓊脂的固體形式人工配製的適合微生物，如細菌或真菌以及組織培養生長要求的混合營養物質。 -
In order to investigate the tolerance of ectomycorrhizal fungi to heavy metals in vitro, three culture methods, namely liquid culture without agitation, liquid culture with agitation and solid agar culture, were investigated to determine which method would give the best combination of fungal biomass and ec50. the results indicated that liquid medium without agitation was the best culture method
為研究外生菌根真菌本身對重金屬污染的耐性，比較了液體靜置、液體搖床和瓊脂固體培養這三種常用的菌絲體的純培養方法，以真菌生物量大小和分離難易程度為主要指標，篩選出液體靜置方法為最優方法。 -
The results showed that the growth of root tips in liquid medium was better than that in agar - solidified medium and solid - liquid two phase medium, for that increasing agar concentrations in medium will reduce the root growth ; darkness was beneficial for fraxinus mandshurica root tip culture in vitro ; as the carbon sources, sucrose was better than glucose and maltose as the carbon sources, and 3 % sucrose was best for the root tip growth of fraxinus mandshurica
結果表明，不添加瓊脂的液體培養基對根尖的生長較添加瓊脂的固體培養基和固液培養基好，原因是增加瓊脂的量會抑制根的生長；暗培養比光培養更有利於水曲柳離體根尖的培養；蔗糖作為碳源的效果較果糖和麥芽糖好，其中以3 %的蔗糖對離體根尖的生長效果最好。 -
Bap performed more important function than kt in differentiation of tall fescue embryogenic calli, but better results could be achieved with combination of 2mg / l bap and 0. 5mg / l kt. at this cytokinin level, 0. 5mg / l naa was recommended to obtain the highest callus regeneration frequency. plant regeneration could be evidently boosted when embryogenic calli were pre - differentiated on high - osmoticum medium with 60g / l sucrose, and / or when the pre - differentiated compact calli were differentiated on differentiation medium solidified with l0g / l agar
高羊茅胚性愈傷組織分化時， bap的作用要比kt大，但2mg lbap與0 . 5mg lkt配合可獲得更佳的效果；在該細胞分裂素水平下，生長素naa用0 . 5mg l ，愈傷組織再生率最高；胚性愈傷組織先在含60g l蔗糖的分化培養基上高滲預分化，以及經高滲預分化后的緻密愈傷組織在瓊脂濃度為10g l的分化培養基上分化，能明顯促進愈傷組織的植株再生；在分化培養基中添加脯氨酸導致愈傷組織再生率下降，但同時有減少白化苗再生的趨勢。 -
High sucrose and agar is apt to keep the tight close structure of callus. ( 4 ) the optional inducing medium of adventitious buds is ms basal medium with 2mg / l 6 - ba, 30g / l sucrose and 9g / l agar. all the tested genotypes have high inducing rate on this medium
供試的4個基因型在此培養基上不定芽誘導效率均最高，由高到低依次為：松93 - 8為962 . 9 ；東農v10為679 . 7 ；東農419為542 . 5 ；富士光為482 . 6 ，與其它處理差異達到顯著。 -
2 established the regeneration system with mature embryos of rice ( 1 ) the optional inducing medium of callus is ms basal medium supplemented 3mg / l 2, 4 - d, 30g / lsucrose and 8g / l agar. ( 2 ) the rate of callus induction varied with the genotypes. dongnong v - 10 has the highest inducing rate among 4 tested genotypes, up to 96. 1 % ; the second is song 93 - 8 and dongnong 419, and the average inducing rate renched 88. 9 % and 88. 3 % respectively
（ 2 ）不同基因型愈傷組織誘導率有差異，供試的4個基因型中，東農v10誘導率最高，平均誘導率達到96 . 1 ；其次是松93 - 8和東農419 ，平均誘導串分別為88 . 9和88 . 3 ；富士光誘導率最低，平均誘導率為78 . 9 。 -
These hairy roots grew well on ms agar medium or liquid medium withour growth regulator for over one year. they grew vigorously and produced numerous lateral branches. four hairy root clones, namely tra1, tra2, tra3 and tra4, were established
毛狀根能在不含任何激素的ms固液體培養基中快速生長，且表現出多分支，多根毛，失去向地性生長等典型毛狀根特性；建立了tra1 ， tra2 ， tra3 ， tra4四個毛狀根無性系。 -
The phenomenon of vitrification phenomenon is a big obstruction in the propagantion of carnation by tissue culture, the effective way to decrease the vitrification phenomenon is to increase the concentration of sucrose and agar in the medium, to use strong luminosity of 10000 - 20000 lx, and to decrease the concentration of hormone
摘要香石竹試管苗玻璃化現象給試管苗的應用帶來困難，採用強光照10000 - 20000lx ，在培養基中提高蔗糖和瓊脂濃度，降低激素用量，對克服香石竹試管苗玻璃化有明顯效果。
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