oligo- -glucosidase 中文意思是什麼

oligo- -glucosidase 解釋

  1. Study on oligo - tnt expanded ammonium nitrate seismic explosive columns

    少梯膨化硝銨震源藥柱的研究
  2. Chitinase forming strain is a kind of special microorganisms. this strain can utilize chitin as carbon source to survive and repoduce. and it has the common biochemical ch aracteristics of secreting chitinase. chitinase can degrade chitin into chitin oligosaccharide, chitin disaccharide, and chitin monosaccharide. the application of chitinase and chitin oligo saccharide on plant resistance are extensively reported. moreover researches verified that c hitin oligosaccharide can promot the growth of plant. so chitinase froming strain is a kin d of promising fungi - resistant microorgnanism. therefore, it ' s a very meaningful work to d o more extensive and deeper researches in this respect

    而幾丁質酶和幾丁寡糖在植物抗病上的應用已經被廣泛的報道，而且有研究證實幾丁寡糖還能促進植物的生長發育。幾丁質酶產生菌是一類很有前途的抗真菌的微生物，因此，在這方面作更廣泛更深入的研究是很有意義的工作。
  3. Soybean oligo saccharide granules

    大豆低聚糖顆粒
  4. Total cellular rna were extracted, 40 micrograms of the total rna were used in the reverse transcription reaction, using superscript ii reverse transcriptase, oligo ( dt ) i8 primers, and cy3 - dctp or cy5 - dctp for the experimental and control group respectively. the labeled cdnas were hybridized to microarrays at 42c for 12 h - 18 h

    提取as _ 2o _ 3作用k562細胞前後的總rna ，用superscript逆轉錄酶逆轉錄成cdna第一鏈，並在逆轉錄的過程中，用cy3 cy5熒光染料分別標記對照組處理組，與自製的k562細胞基因表達譜晶元雜交。
  5. Total rna was extracted from the second stage larve of hypoderma sp, then single chain cdna was synthesized by reverse transcription using oligo ( dt ) 18 as a primer. the hypodermin c ( hc ) and hypodermin a ( ha ) gene specific primers were devised by dnastar software

    本試驗的目的旨在進行hypodeminc （ hc ）和hypodermina （ ha ）基因的克隆、測序、構建重組表達載體並誘導表達，獲得重組抗原，以解決天然抗原的不足並為診斷和免疫試劑的產業化奠定基礎。
  6. Insecticidal activities with chitosan and oligo - chitosan

    殼聚糖殺蟲與殼低聚糖抑菌活性研究
  7. In this paper, the research progresses of several high additional co - product, such as furfural, xylose, xylitol, oligo - xylose, fuel ethanol and soon, produced with cod through the biorefinery are reviewed

    概述了利用生物煉制技術用玉米芯生產糠醛、木糖、木糖醇、低聚木糖和燃料酒精等一系列高附加值產品的研究進展。
  8. Constructing cdna expressing library of erythrocytic plasmodium falciparum from hainan : the total rna was obtained by using. triplix kit. a modified oligo ( dt ) primer ( cds ffi pcr primer ) was used in the single - stranded ( ss ) dna synthesis reaction. the ss - dna was reversely transcripted from total rna. double - stranded ( ds ) cdna was amplified by long - distance ( ld ) pcrafter the digestion with proteinase k and sfi i, the cdna with no less than 200bp was collected and purified by glass - milk kitthe library was constructed after the ligation of cdna to tiplex2 phage particle packaged with the packaging extract system in vitro. a high titer and high recombinant ratio of cdna library was constructed

    構建惡性瘧原蟲海南株紅內期cdna表達文庫提取紅內期惡性瘧原蟲海南株總rna ，直接以總rna為模板使用cdna文庫構建試劑盒，首先反轉錄合成ss一dna ，再擴增合成ds一dna （ cdna ） ，對擴增產物用蛋白酶k消化及左z丁i酶切，抽提蛋白、去除rna后，用玻璃奶試劑盒純化、回收20obp以上的片斷，經與載體連接再用蛋白包裝物包裝后形成未擴增文庫，最後擴增完成惡性瘧原蟲海南株紅內期cdna表達文庫的構建。
  9. An oligo - nucleotide primer was designed according to a conservative fragment of this gene of plants in genebank. two 3 ' - end coding sequences of this gene ( including complete sequences of exon 8, 7, 6, 5, 4 and partial sequences of exon 3 ), one, 1097bp, and the other 1109bp, were successfully isolated from brassicaeae napus and brassicaeae campestris. the dna sequence analysis shows that the two fragments are more than 90 % identical to orychophragmus violaceus, arabidopsis thaliana and brassicaceae napus

    同源對比分析已有的植物epsps基因序列，我們找到了該基因中一段極為保守的序列並設計了一條寡核苷酸引物，採用3 』 race法，從植物蜀雜9號油菜，白菜型油菜總rna中成功的擴增出了epsps基因3 』端編碼區（包含外顯子8 、 7 、 6 、 5 、 4的全部序列及外顯子3的部分序列） ，分別長1097bp ， 1109bp 。
  10. A pair of primers were designed according to the published sequence of gnrh2 ' s gene mrna and transporter gene with oligo version 4. 1 softwarre, they were annealed by their 3 ' terminal brief complementary base sequence to form small segment double chain, therery, they serve mutually as template and primer, and their extension were carried out to synthesize 90 bp " gnrh / trs

    本研究根據genbank中已發表的人gnrh2基因mrna序列以及轉運肽（ transporter ， trs ）基因核苷酸序列，藉助oligo4 . 1設計了一對寡核苷酸引物，以引物3末端的短互補序列退火形成小段雙鏈，從而互為模板和引物，通過引導合成長達90bp的gnrh trs序列gnrh trs 。
  11. According to the reported complete vp6 nucleotide sequences of group a prv in genbank, a pair of primers was designed to amplify vp6 gene of jl94 with oligo 4. 1 software. the segments of complete gene 6 of jl94 were obtained from rt - pcr using dsrna extracted from the virus as template

    根據genbank中的多株豬a群輪狀病毒vp6蛋白完整基因序列，利用oligo4 . 1設計引物，以jl94rna為模板，通過rt - pcr擴增出長約1 . 3kb的基因片段，命名為vp6 。
  12. Effect of yangjing - recipe on immunological function of kidney and liver insufficiency patients with oligo - astheno spermia

    弱精子癥肝腎虧虛患者免疫功能的影響
  13. According to csfv ' s e2 gene sequence published in genbank and the sequence of p. pastoris expression vector ppic9 ' s multiple cloning site ( mcs ), a pair of primers were designed with oligo and primers. o softwares

    將該基因片段先克隆到pmd18 - t載體上，並進行了酶切、 pcr鑒定和測序分析，陽性重組質粒命名為t - e2 。
  14. Genes coding mature peptide of igfs were achieved by pcr using another pair of oligo - nucleotide primers to induce to the suitable restriction enzyme site, and the igf - i product of pcr contains 230 base pairs. igf - ii contains 219 base pairs. 3

    各另外設計一對特異性pcr引物，導入適當限制性內切酶切點，以上述連有目的基因的克隆載體為模板，採用pcr方法擴增基因片段，獲得長度約230bp的igf -和219bp的igf -成熟肽基因序列。
  15. The construction of pci - il - 2 : primers were designed by the software oligo, xhol and sail were added to the primers, the cdna of il - 2 was obtained by pcr. the cdna of il - 2 was ligated with pci - neo cleaved by xhol and sail. the recombinant was evaluated by pcr

    Pcr法擴增幾億片段，在t4連接酶的作用下與xhol和sal工酶切的pci neo載體連接， pcr法鑒定重組體，用xho工， xhol sal ， ban工工酶切進一步驗證重組體，命名為pclll 2 。
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