plate culture 中文意思是什麼
plate culture
解釋
平面培養-
Monokaryons of this fungus will grow readily as saprophytes in plate or liquid culture.
這種真菌的單核體在平板或液體培養時能像腐生菌那樣容易生長。 -
These cells displayed metabolic disturbance, such as rough cytoplasmic granules, many vacuolation. nearly all cells in the common medium showed cytoretraction and pyknotic nuclei, and were detached from the plate after 5 - 7 days of culture. while most hepatocytes in special medium showed well condition
普通培養液組的肝細胞伸出的偽足數目較少，細胞多呈三角形或梭形，細胞胞體較小，透光度差，且死細胞較多，高倍鏡下觀察細胞胞漿內有粗大的顆粒狀物質，並且有大量的空泡，細胞呈現代謝不良的狀態。 -
The free living and particle - attached bacteria groups are significantly different in term of species composition. plate culture strains are different from dominant field groups. this result proved the insufficiency of traditional cultural methodology
適合於在平板培養條件下生長的類群並非湖水中的優勢類群，這一結果進一步證實了傳統的培養方法在分析水體細菌群落生物多樣性方面的不足。 -
The main products of our company are : complex bag, card head bag, hdpe, pe, pp compound bag, electricity carve plate making color printing bag, nylon vacuum fresh bag, the pvc product, and so on. its suitable for the packing of light industry, engine, chopsticks, sanitary ware, shoes and cap, toy, exquisite article, decoration, culture things, etc. we can provide the packing material according to the customers request
公司的主要產品有：復合袋卡頭袋hdpe pe pp電雕製版彩印袋以及尼真空保鮮袋和pvc製品等等，適合輕工機械筷子衛浴鞋帽玩具精品裝飾文化用品等行業包裝之用。 -
After electrophorised on 1 % agarose gel, the pcr production was purified with agarose gel dna extraction kit. the segment was ligated with vector pmd18 - t and then was tranformed into the competent cell of dh5 a. a construction mstnd - pmd18t was generated by inserting the sequence of 254bp into pmd18 - t vector and selecting the sense clones. positive clone was identified by three ways : endonuclease digestion, pcr and sequencing. the result showed that the cloned sequence coincides with the designed sequence. this construction was digested with nco i and xho i and ligated the pet28a ( + ) vector digested with the same enzymes using dna ligation kit. the production of ligation reaction was transformed into the competent cell of bl21 ( de3 ). after 12 - 16 hours of culture, several colnes appeared on the plate. some positive clones were selected to extract their plasmid. these plasmids were digested by nco i and xho i and indentified by pcr. a contraction, mstnd - pet28a was generated. the result showed that the cloned sequence coincides with the designed sequence
F _ 1長38bp ， r _ 1長36bp ，其它片段均40bp長， f _ 1和r _ 1片段兩端分別加上限制性內切酶nco和xho的識別位點序列。用成對單鏈片段進行延伸反應，然後用其他單鏈片段作為引物，進行pcr擴增，用dna快速純化回收試劑盒回收所得254bppcr產物，與pmd18 - t載體連接、轉化dh _ 5 。受體菌感受態細胞，利用藍白斑遺傳學篩選法篩選陽性克隆，提取其質粒，採用nco和xho雙酶切鑒定，獲得了254bp的片段；用pmd18 - t載體上的特異引物rv - m和m13 - 47進行pcr鑒定，獲得300bp的片段。 -
Mathematical culture is in the new mathematics curriculum standard as a new and independent plate
摘要在數學新課程標準中，數學文化作為新增加的一個獨立板塊被明確提出。
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