活酵母細胞 的英文怎麼說

中文拼音 [huójiàobāo]
活酵母細胞 英文
living yeast
  • : Ⅰ動詞1 (生存; 有生命) live 2 [書面語](救活) save (the life of a person):活人無算 (of a goo...
  • : 動詞(發酵) ferment; leaven
  • : Ⅰ名詞1 (母親) mother 2 (泛指女性長輩) one s elderly female relatives 3 (配套的兩件東西里的凹...
  • : 形容詞1 (條狀物橫剖面小) thin; slender 2 (顆粒小) in small particles; fine 3 (音量小) thin ...
  • : Ⅰ名詞1 (胞衣) afterbirth2 (同一個國家或民族的人) fellow countryman; compatriot Ⅱ形容詞(同胞...
  • 酵母 : yeast酵母浸液[提取液] yeast extract; 酵母聚糖 zymosan; 酵母片 aluzyme; 酵母細胞[植物] yeast plant; yeast cell
  • 細胞 : cell; sytes; bioplast; cella; [口語] gene; [生物學] cellule; cellule cellulli cellulo ; cello ; k...
  1. Even so, by truncating hbv pres gene, we finally obtained some useful " " bailors ", either nontoxic or self - activating, and used them to fish dna fragments of hbv pres interacting protein ( s ) from an ad vector constructed human embryonic cdna library

    我們通過第回軍巨大學碩士學位論文對pres基因分段截短的方法,獲得了對即無毒性作用,又沒有自激作用的「誘餌」 ,通過它在雙雜交系統中篩選構建於ad載體的人胎肝。
  2. The hemolytic activity was mg2 + - dependent and heat - sensitive, and was abrogated by treatment with rabbit anti - human c3 serum, zymosan, methylamine, hydrazine, and phenylmethylenesulfonyl fluoride ( pmsf )

    文昌魚體液對兔血紅的溶血性在受到聚糖、甲胺、肼、 pmsf 、 edta 、兔抗人補體3抗血清處理時,溶血性消失。
  3. The deleted mutant pap gene was also cloned into yeast secreted expression ppic9k vector to form ppic9k ~ 3, then the vector was transferred into pachia pastoris gs115 strain. the specific expression protein was secreted into the medium after inducing with methanol and the protein amount reached about 50 - 60 u g per millilitre measured by uv - absorbed methods in the supernatant of the medium via high density fermentation. sds - page results showed that there was one protein band in the gel which molecular weight was about 34ku

    將缺失型pap基因克隆于分泌型表達載體ppicgk構成重組載體,然後導入畢赤( p8chianastoris )菌株gslls中,在甲醇的誘導下,經過高密度發進行pap的表達,經sds page分析,結果表明,在培養基上清液中含有一明顯的特異性蛋臼條帶,大小為34ku ,經western blotting分析,該蛋白與法國pap抗血清有特異性反應,體外性檢測表明該蛋白對tmv的侵染性具有高度的抑制性,說明該pap基因在畢赤gs中也得到了正確表達。
  4. Biological assay proved that the expressed product could stimulate the proliferation of cd34 + hematopoietic cells. conclusion : flt - 3 ligand extracellular domain was successfully expressed

    體外性實驗表明,畢赤氏表達的重組fl蛋白可以有效地刺激造血幹cd34 「的增殖。
  5. The results indicated that the content of cytosolic cam in cells treated with exogenous ca2 + has increased indistinctively, while fluorescence intensity in cells treated with tfp decreased. so we believed that exogenous ca2 + has little effect on the expression of cam

    結果發現,經過外鈣處理的內cam的表達量有所增加,但並不明顯,因此認為增加外鈣濃度對內cam的表達影響不大,但使處于化態的cam相應增加。
  6. 5 statistic treatment with spss soft. results after treatment with mms at various ( 0. 01 ~ immol / l ) concentration for 72h, we examined s. cerevisiae s288c cells for dna - damage situation and changes in telomerase activity

    5統計學處理結果將不同濃度的mms ( 0 . 01一1 ~ fl )作用於釀酒5288c72h后,分別檢測其dna損傷程度及端粒酶性變化。
  7. Our aim was to investigate the effect of carcinogen mms on dna and telomerase activity of s. cerevisiae s288c and provide some scientific foundation for the relation between telomerase and cancer

    本研究旨在觀察致癌劑mms對釀酒s288cdna損傷反應以及對端粒酶性的影響,為端粒酶與惡性腫瘤的關系提供科學依據。
  8. Recent reports showed that telomerase activity in s. cerevisiae cells could be significantly up - regulated after exposure to some dna - damaging agents, which may be related with dna - damage repair

    端粒酶與生長、繁殖、衰老及腫瘤的發生密切相關。近來研究發現,釀酒經dna損傷劑作用後端粒酶性升高,可能與端粒dna損傷后修復機制有關。
  9. We found that there are two types of map1lc3 in rat, mouse and human, besides that, there is another type ( map1lc3c ) in human. we expressed all map1lc3 in hek293 cells respectively and found that the post translational modification of all map1lc3 is similar to yeast apg8 and rat map1lc3 identified except human lc3b. characteristic carboxyl cleavage occurred in conserved glycine of them

    在hek293中分別表達這三個物種中的所有的a型、 b型以及人map1lc3c分子,發現除了人的map1lc3b外其它同源物的修飾方式與已知的apg8和大鼠的lc3修飾方式相類似,均發生了羧基端的切割反應而且羧基端保守的甘氨酸是它們發生翻譯后修飾的性位點。
  10. When mms was added directly to s. cerevisiae s288c cell extracts immediately before primer addition, telomerase activity remained unchanged. thus, a direct influence of mms on trap assay does not seem to be involved in telomerase activation observed after drug treatment

    如果在加人引物之前將mms直接加在釀酒5288c蛋白提取物zh ,結果顯示端粒酶性沒有變化,因此排除了mms對端粒酶的直接激作用。
  11. In our work, different hbv pres gene fragments were amplified by pcr, cloned into pgbkt ? vector in yeast two - hybrid system 3, and then transformed ah 109 yeast cells. the results showed that these pres expression products were nontoxic to yeast cells, but all self - activated the yeast two - hybrid system

    本研究將hbv前s區不同片斷進行擴增,克隆入雙雜交系統3中的pgbkt7載體,轉化ah109 ,經檢測,證實了hbv前s區不同片斷對無毒性作用,但是都存在自激作用。
  12. Its activity was strongly against to yeasts such as candida albicans, cyptococcus neoformans, not to filamentous fungi. it showed activity against positive and negative bacteria and no cell toxicity

    其抑制作用主要針對白色念珠菌,新性隱球菌等類真菌,而對絲狀真菌幾乎沒有抑制作用;具有廣譜抗性;幾乎沒有毒性。
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