growth promoter 中文意思是什麼
growth promoter
解釋
生長促進劑-
The insulin - like growth factor - 2 ( igf - 2 ) and igf conjugated protein - 6 ( igfbp - 6 ) mrna level in rat calvaria bone tissue and mc - 3t3 - el cells were detected by northern blotting analyses and reverse transcription polymerase chain reaction. the estrogen responsive element ( ere ) in igfbp - 6 gene promoter was identified and involved in tcdd - reduced regulation of the gene expression by electromobility shift assays ( emsa )
正常胎鼠頭蓋骨組織igf一2mrna呈高水平表達狀態，而igfbp一6mrna的水平較低; ccf胎鼠頭蓋骨骨組織內igf一2mrna的表達較正常胎鼠降低， igfbp一6mrna的表達則明顯升高; atra和e :聯合應用時， atra可以抑制雌激素對細胞內igf一2和igfbp一6的這種調節作用。 -
Growth factors can act on many kinds of cells as mitotic promoter and deprival of growth factors can cause cease of cell growth or cell death. thus growth factors are usually thought relative to cell growth and differentiation
生長因子可以作為促分裂劑作用於多種細胞，剝奪生長因子可以導致細胞生長停止或細胞死亡，因此通常認為生長因子與促進細胞的增殖和存活有關。 -
Driven by the cauliflower mosaic virus ( camv ) 35s promoter, the er - shsp over - expressed constitutively. the growth and the phenotype of transgenic plants can be used for researching the function of er - shsp in improving tomato ' s cold resistance and the er - shsp chaperones function in vivo. after degested by kpnl and xbal enzymes from the pbs - er plasmid, the gene er - shsp - lehsp21. 3 was inserted into the prokii vector to construct an eukaryotic expressing vector
利用基因工程方法，將內質網小分子熱激蛋白基因（ endoplasmicreticulum - locatedsmallheatshockproteingene ， er - shspgene ） - lehsp21 . 3導入到番茄體內，使之在植物體中組成性表達（ constitutiveexpression ）內質網小分子熱激蛋白（ er - shsp ） ，觀察轉基因番茄在低溫條件下的生長和表型反映，研究er - shsp在提高植物耐寒性中的作用，同時為體內研究er - shsp的分子伴侶機制提供依據。 -
Abstract : determined the power - time curves of the promoter bacteria of ganoderma lucidum for e. coli, using 2277 thermal activity moniter, a new experimental model of promoter bacteria growth were established. the growth rate constant and heat output at different concentration of ganoderma lucidum have been calculated. from - c and q - c curves the optimum concentration has also been established
文摘:用熱活性檢測儀測定了天然藥物靈芝對大腸桿菌起促菌作用的熱功率-時間曲線，並根據曲線建立了細菌生長的新的實驗模型，按新模型計算了促菌作用下的生長速率常數，發熱量及最佳促菌濃度。 -
Expression of atnced3 driven by 35s promoter, rd29a promoter or kst1 promoter has greatly affected the growth and stomotal movement and drought tolerance in the transgenic tobacco plants. we observed the 35s : iatnced3 plants showed severe growth retarda - tion, and vd29a : atnced3 plants exhibited slight growth retardation, however we also observed the kst1 : : atnceds plants had a good growth under normal conditions
比較了35s 、 rd29a 、 kst1啟動子驅動atnced _ 3的表達對煙草生長和氣孔運動以及抗旱性的影響，結果表明35s轉基因植株明顯生長矮小，發育滯后； rd29a轉基因植株生長也比野生型慢一點； kst1轉基因陽性苗表型最好，在正常條件下生長旺盛。 -
Our results showed as follows : 1 ) the spl and rsal polymorphisms of the collagen type 1 alpha 1 ( col1 al ) gene, the - 174g / c promoter polymorphism of the interleukin - 6 ( il - 6 ) gene, the asn363ser polymorphism of the glucocorticoid receptor ( gr ) gene, and the t ? c polymorphism in intron 5 of the transforming growth factor pi ( tgf - p ! ) gene are absent or too rare in chinese. compared the polymorphisms of these five markers with other populations using % 2 test and fisher ' s exact two - tailed test, significant differences of allele and genotype frequency distributions were observed at these polymorphisms ( p < 0. 001 )
結果表明： 1 ）白介素6 （ il ? 6 ）基因的? 174g c多態性、型膠原蛋白_ 1 （ col1a1 ）基因的sp1和rsa多態性、轉化生長因子_ （ tgf - _ 1 ）基因的內含子5t c多態性和糖皮質激素受體（ gr ）基因的asn363ser的多態性在中國人群中均未發現或者多態性很低； x ~ 2檢測和fisher精確（雙尾）檢驗比較這些多態性的頻率，發現在中國人群與其它種群或人群中，等位基因和基因型存在顯著的差異（ p 0 . 001 ） 。 -
And then a 378bp acci fragment in pbtk2. 6 was replaced by a fragment containing the immediate early promoter of cytomegalovirus and bovine growth hormone polyadenylation signal derived from pcr3 - uni, a eukaryotic expression plasmid
在此基礎上，進一步用tthlll酶切后，補平插入帶有sv40啟動子的大腸桿菌?半乳糖苷酶報一告基因（ lacz ） ，獲得通用轉移載體pltk - uni 。 -
Zhonghua 11 ) at different growth phases. so, the promoter region ofosdd2 gene was cloned and fused with a gus gene, in order to speculate the osdd2 expressing patterns
鑒于基因表達模式不清，克隆了osdd2基因約2kb左右的啟動子序列並與gus基因融合，構建植物轉化載體。
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