溶液培養 的英文怎麼說
中文拼音 [róngyèpéiyǎng]
溶液培養
英文
aqua culture-
In the 2 - step ops method, embryos were pretreated with 10 % eg + 10 % dmso for 30s before exposed to edfs30, a vitrification solution, for 25s, then immersed in liquid nitrogen. the blastocyst rate of vitrified mouse morula after equilibration in 0. 5mol / l sucrose for 5min was 100 %
Ops二步法即胚胎預處理30s ,然後移入edfs30冷凍液中平衡25s冷凍保存,解凍后在0 . 5mol l蔗糖溶液中平衡5min ,培養后囊胚發育率為( 100 ) 。Fluoride treatment included both excised leaves cultured in nutrient solutions and leaves from plants fumigated with hf.
氟化物處理既包括培養在營養溶液中的切離葉片和HF熏氣的植株上來的葉片。And for those who prefer a healthier diet there is also a hydroponic greenhouse where fresh vegetables will grow all year round
還為那些注意健康飲食者建造了溫室,溫室內熟菜用溶液培養,新鮮綠色食品一年四季絡繹不絕。Pcr amplification using 2 degenerate primers for nitrogenase fe protein gene was performed with chromosomal dna isolated from the 29 isolates. the result suggested that a nifh amplicon of 323 nucleotides was detected in 7 isolates and the 7 isolates are c4 c5 g1 g2, w5 t1 and t7. these pcr amplified fragments were cloned, and sequenced
首先利用芽孢桿菌中芽孢的抗熱性將土壤溶液在100沸水中煮10 - 15分鐘,然後用選擇性無氮培養基進行初篩得到29株菌落形態不同的菌株;接著用固氮酶結構基因nifh的特異性引物對這29株菌進行pcr擴增,結果表明其中7個菌株具有nifh基因,這7個菌株的編號依次為: c4 、 c5 、 g1 、 g2 、 w5 、 t1和t7 。In the ht medium with 2 % starch, after the strain nust03 had been culturing on a rotary shaker at 28, 220r / min for 96 hours, the fermentation can restrain the growth of a. niger
Nusto3菌株在含有2的可溶性澱粉的ht培養基上,搖床( 28 , 200r min )培養96小時,發酵液對黑麴黴有抑制作用。Influence of soluble phosphate on rock phosphate solubilization by filtrate of phosphate - solubilizing fungi
可溶性磷含量對溶磷真菌培養濾液溶解磷礦粉的影響Method four bacteria were separately cultured and measured the transparent circle after adding the lodine solution
方法將各菌種接于澱粉酶試驗培養基,培養后滴加稀碘溶液,觀察透明圈,判定產酶能力。But most papers addressed mainly the mechanisms of al toxicity and tolerance in plant root system, because inhibition of root growth is one of the earliest symptoms of al injury and the most easily recognized symptom in solution culture
然而,大多數文章主要綜述鋁對植物根系的影響及其耐性,因為根生長受抑是最早的鋁毒害癥狀之一和溶液培養時最容易辨認的鋁毒害癥狀。Calli were induced by culturing hypocotyls of pepper in the ms medium supplemented with 2. 0mg / l 6 - ba and l. omg / l naa. the diploid wound callus was treated by adding colchicines into the medium and by immersing into colchicines solution for different concentrations and periods
通過將不同濃度的秋水仙堿加入培養基和不同濃度的秋水仙堿溶液浸泡兩種方法處理愈傷組織,從而篩選出最佳的誘導方法和最佳的秋水仙堿濃度和處理時間。And considerable work has been done hi the growth behaviour in the tetrachloride solution concluding studies of crystal growth and growth kinetics. a crystal of dimensions 20mm x 20mm x 1mm was produced hi the tetrachloride solution by lowing temperature. and bcf spiral growth mechanism for the surface diffusion model was analyzed using the kinetic data
本文以苯為溶劑溶液降溫法培養出了60mm 40mm 3mm大尺寸hhm單晶;另外探討了hhm在四氯化碳溶液中的生長行為,溶液降溫法培養出了20mm 20mm 1mm的較大尺寸單晶,並用動態循環體視顯微鏡觀察法測定了其在不同的過飽和下主要顯露晶面的法向生長速率,在較大過飽和度范圍內考察了其bcf表面擴散螺位錯生長機制。Flexor digitorum profundus tendons of chickens wer e cultured in the presence of deoxyguanosine ( dgua ) for 5 days, then cryopreserv ed in liquid nitrogen ( 196 ) without affecting their viability
用脫氧鳥苷培養處理雞屈趾深肌腱5天,無創凍存於液氮貯存器( 196 )中3個月,使用前將凍存腱在40溶液中融解並洗去腱中吸收的二甲基亞碸。5. effect of recovery methods after thawing after thawing, the highest viability was obtained when beads of pavlova viridis were incubated in culture medium for 48h in darkness at room temperature. as to other two algae, the suitable recovery method was to incubate beads over saturated nacl solution in a closed jar for 12h in darkness at room temperature
( 5 )化凍后恢復方法的影響化凍后,綠色巴夫藻的膠球在培養基中室溫下暗放置48h后存活率最高;另兩種金藻在含有過飽和的nacl溶液( 75 % rh )的密閉氣相中室溫下暗放置12h存活率最高。It was found from the culture condition, morphological characters, and preservation condition of c. elegans that c. elegans grew well at 16 on the ngm culture medium and can be preserved for two months in the liquid of 30 % glycerol at - 80
通過對秀麗隱桿線蟲形態、培養條件以及保存方面的研究,發現秀麗隱桿線蟲在16 ngm培養基中生長良好,將其放入30 %甘油溶液中,在- 80冰箱中可以保存較長的時間。Fluoride treatment included both excised leaves cultured in nutrient solutions and leaves from plants fumigated with hf
氟化物處理既包括培養在營養溶液中的切離葉片和hf熏氣的植株上來的葉片。Because d. salina can grow in high salinity environments, where the other organisms survive hardly, large - scale culture of d. salina do not need expensively fermentive or other special equipments, suggesting that d. salina is a favorable host for producing pharmaceutical proteins
由於杜氏鹽藻可在高滲鹽溶液中生長,這是許多其它生物難以生存的環境,故其大規模培養不需昂貴的發酵罐或其他培養裝置,可以直接採用開放式培養,大大降低生產成本。The results showed : the best additive water to wheat bran solid medium was 35 percent. a. niger an01001 produced high activity phytase when it was cultivated at 30 ? from 90 to 120 hours, and obtained the highest enzyme activity at 114 hours. phytase activity was effected by different buffer and ph, enzyme activity was high at ph 5. 5 and 6
對該菌的產酶條件進行研究的結果表明:麩皮固體培養基的最適加水量為35 ; 30培養90 120h之間產酶都比較高,在114h酶活最高;在提取時不僅ph對酶得率有影響,而且不同提取液所要求的最適ph也不同,用乙酸緩沖液提取時,當ph為5 . 5 、 6 . 5時酶活較高,進行水提取時,在ph7 . 5時酶活最高;利用cacl _ 2溶液進行提取的濃度達到3時,酶活最高。分享友人