taq 中文意思是什麼

taq 解釋
安其拉神廟
  1. Among the three methods used in the experiment of dna extraction, only ctab, adding pvp in the dna isolation step, had effectively reduced the disturbance from fiber or other plastids and extracted suitable genomic dna as template for rapd process. pcr amplifications were performed in a final volume of 25 mm3 containing 0. 5 units taq polymerase, 2

    通過在抽提緩沖液加入2的pvp 、並用異丙醇和乙醇沉澱基因組dna等改良措施， ctab法能避開大量纖維、多糖的影響，有效地從不同屬種的棕櫚科植物的幼嫩葉片中提取並純化了適合rapd的基因組dna 。
  2. Taq i could distinguish p. abalonus and p. cystiodisus from the other pleurotus, but p. abalonus and p. cystiodisus could n ' t be differentiated for each other. msp i had the highest polymorphism and could divided 52 isolates of pleurotus into 8 groups, 5, 5 and 4 groups for hae iii, hint ], hha i in all isolates of pleurotus. cluster analysis based on pcr - rflp of 28s rdna 5 " half suggested that five groups were distinguishable for all isolates of pleurotus on 92 % similairity coefficient level, i. e. i p. djamor and p. salmoneoslramineus, p

    28srdna5 』端擴增產物的酶切分析表明，所有供試側耳菌株無alu酶切多態性， bamlh可將金頂側耳與其它供試側耳分開， taq可將鮑魚菇和囊蓋側耳與側耳其它供試側耳菌株區分開，而鮑魚菇和囊蓋側耳則不能分開， msp酶切多態性最強，可將供試側耳分為8種基因型， hae 、 hinf和hha次之，分別可將供試側耳分為5種、 5種和4種基因型。
  3. That is to add a special fluorescence - based dna internal standard in the telomerase elongated ts primers, then do pcr amplification after a step of refinement ( hydroxybenzene / chloroform extracting, and deposited by ethanol ). sequencing analysis of pcr product was done on 310 gene scan analysis ?. 1. 2 dna sequencer to determine telomerase activity. notably, this method eliminated the restraining factors of taq dna polymerase, making it possible to erase the sample differences met in pcr and eradicate the annoying phenomena of pseudo negative results

    在kim等開發的端粒重復擴增分析法（ trap ）的基礎上進行改進，即通過對端粒酶延伸ts寡核昔酸反應產物的精製，消除了pcr擴增中抑制taq酶活性的因素，從而減少了樣品之間pcr擴增上的差異和假陰性現象的發生，提高了判斷樣品端粒酶陰、陽性的準確率和定量的準確性。
  4. Due to high sensitivity of rapd analysis to reaction conditions, main factors affecting the results including composition of the buffering system, concentrations of taq dna polymerase, primers and templates, and number of pcr cycle etc., were examined, and conditions applicable to rapd analysis of j. curcas were determined

    針對rapd標記影響因素眾多、結果重復性低的特點，對rapd分析中pcr擴增的各種條件進行了梯度測試，包括反應混合液成分、 taq酶量、引物濃度、模板濃度、 pcr循環數等。
  5. The y - a489 - plex multiplex pcr is feasible for using home product of taq dna polymerase

    Y一a489一plex體系採用的是國產的taq酶。
  6. Furthermore, the home product of taq dna polymerase had the same specificity and efficiency compared to the amplitaq gold ( pe, usa ) in this study. conclusion this is the first time that the tailed primer design protocol for multiplex pcr system is used for y - str loci

    初步構建了四個y一str基因座的y一a489一plex銀染體系和y一a4sg一plex熒光體系:並依據dna分析技術工作組（ twgdam ）指南進行了應用性研究。
  7. 6. the restriction analysis of its amplified product showed that no restriction site was observed for bamh i in all isolates, the other tested enzymes ( alu, hae iii, hinf i, taq i, hha i, msp i ) could distinguish p. cilrinopileatus from the other pleurotus species

    6 . [ ts擴增產物的限制性酶切分析結果表明，召til ） ， hl對所有供試菌株均無酶切位點，而另外6利，供試內切酶（ alul 、 haeitl 、 llllal 、 11infl 、九式斗， i 、 tcl叮i ）都能將金頂側耳與其它側耳菌株區分開。
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