- 更多网络例句与毒基相关的网络例句 [注：此内容来源于网络，仅供参考]
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The compounds 1～6:β-Amanitin、α-Amanitin、phallisacin、phallisin、phallacidin andphalloidin.As the content of compound7, compound 8 and compound 9 were all to little.
化合物1～6分别为：β-鹅膏毒肽、α-鹅膏毒肽、羧基三羟鬼笔毒肽、三羟鬼笔毒肽、羧基二羟鬼笔毒肽和二羟鬼笔毒肽。
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In all, A.subjunquillea.S.lmai methyl alcohol crude extract were research by high pressure liquidchromatography,.separation and purification obtained to 9 kind of compounds, identified 6 kind ofcompounds. The compounds 1～6:β-Amanitin、α-Amanitin、phallisacin、phallisin、phallacidin and phalloidin.
总之，黄盖鹅膏甲醇粗提物应用高效液相分离纯化9种单体化合物，鉴定6种分别为β-鹅膏毒肽、α-鹅膏毒肽、羧基三羟鬼笔毒肽、三羟鬼笔毒肽、羧基二羟鬼笔毒肽和二羟鬼笔毒肽。
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比如：Adobe、第三只眼网络监控、国内外各种杀毒软件，如卡巴斯基、趋势科技、金山公司杀毒系列，办公系列产品，用友，金碟等国内外著名软件的授权代理，详情请登录我司网址：www.nti56.net
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So it is assumed that the E-box might be associated with the enhancement of transcription activity.Here, the LTRs of WH17 ,DLA-25,DLA-118 and LTR with single mutation in the E-box motif were separately cloned into pCAT-Basic vector resulting in a series of recombinant plasmids containing CAT reporter under the control of different versions of LTRs.
通过对EIAV分离株WH17的LTR与L株、DA和DLA株的LTR序列进行比较，发现其在在U3-R结合处多一个E-box基序，推测该基序的变化可能会起到促进转录作用，为此将EIAV强毒株(DLA-25)、驴白细胞弱毒株(DLA-118)、EIAV分离株WH17以及U3-R结合处的E-box基序点突变的LTR分别克隆到pCAT3-basic质粒中的报告基因氯霉素乙酰转移酶的上游，获得一系列受不同LTR控制的CAT表达质粒。
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In order to develop a safe and effective immunoadjuvant to enhance the immunity and resistance of animals against infection, a novel CpG Oligodeoxynucleotides containing 11 CpG motifs was synthesized and inserted into the VR1012 plasmid, designated as VR1C. Then the recombinant VR1C was entrapped with Chitosan nanoparticles prepared by the method of ionic cross linkage, and employed to inject muscularly 3-weeks old Kunming mice; the blank VR1012 packed with CNP and saline were used to inoculate mice as the control groups. 28 days after inoculation, all mice were orally fed with 0.4ml 2x108CFU/ per mouse virulent hemorrhagic enteritis E. coli to challenge the resistance against infection.
为研制安全高效免疫调节剂增强动物免疫抗病能力，本实验设计合成含11个C pG基序的寡聚核苷酸，重组构建含CpG的VR1012质粒(VR1C)；制备壳聚糖纳米颗粒包裹重组质粒(CNP-VR1C)，肌注接种3周龄昆明小白鼠，设壳聚糖包裹空质粒和生理盐水对照组；接种后28天口服大肠杆菌攻毒观察小鼠天然免疫的变化和对强毒感染的抵抗力，Sandwich ELISA测定血清免疫球蛋白和白细胞介素含量。
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The acute toxicities of 2-chloro-4-nitroaniline, 4-chloro-3-nitroaniline, 2-chloro-5-nitroaniline, 2, 4-dichloroaniline, 3, 4-dichloroaniline, 2, 5-dichloroaniline, 2, 3-dichloroaniline to zebra fish were conducted in lab. 48h LC〓 values were 11. 18, 4. 62, 9. 23, 9. 55, 7. 07, 6. 68, 0.62mg/L respectively, and 96h LC〓 values were 6. 99, 2. 58, 8. 63, 7. 79, 6. 08, 5. 23, 0.49mg/L respectively.
1研究了2-氯-4-硝基苯胺、4-氯-3-硝基苯胺、2-氯-5-硝基苯胺、2，4-二氯苯胺、3，4-二氯苯胺、2，5-二氯苯胺、2，3-二氯苯胺对斑马鱼的急性毒性，经计算48h LC〓分别为11.18、4.62、9.23、9.55、7.07、6.68、0.62mg/L，96h LC〓分别为6.99、2.58、8.63、7.79、6.08、5.23、0.49mg/L，这7种化合物均属于高毒物质。
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By combining 2 chloropyridine, 1,3,4 thiadiazole and acylamide , three toxophoric moieties seven 2 [ N (1 methoxycarbonyl)ethyl N acyl]amino 5 [(2 chloropyrid) 4 yl] 1,3,4 thiadiazoles(8) were synthesized in seven steps.
另外 ，酰胺作为致毒基存在于许多生物活性物质中，特别在除草剂中具有重要地位 [5，6 ]。
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The percentage of active transmission of small brown plant hopper varied with the infection stage of RBSDV in maize cell while the nymph acquiring feeding. There were 2.93% and 7.83% of viruliferous rate resp
用灰飞虱无毒若虫在细胞内病毒基质出现和病毒增殖期饲毒的，到成虫时分别有2.93%和7.83%个体传毒率；在细胞内病毒成串分布于管状结构和晶格状聚集排列期饲毒的，到成虫时均不能传毒。
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Cases taking the medicine for more than 6 months were collected. The changes of Chinese medicine clinical symptoms and signs, the clinical symptoms and signs, the integrals, body weights, cold-catching numbers and CD4 were observed. Results The effective rate, steady rate and ineffective rate of Chinese medicine clinical symptom were 79.52%, 10.84% and 9.63%, respectively.
对云南省疾病预防控制中心确诊的HIV/AIDS 140例患者，根据中医辨证，邪毒内蕴者口服扶正抗毒胶囊，肝脾肾俱虚者口服康爱保生胶囊，选择治疗时间≥6个月的病例共83例，对其中医临床症状、体征，临床主、次症状与体征，卡洛夫斯基积分，体重变化，感冒次数，CD4的变化情况进行临床研究。
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The therapeutic efficacy of hemoperfusion and dimerca prol in rescuing patients with acute tetramine poisoning is better than dimercaprol and routine therapy only.
结论HP联合二巯基丙醇救治急性毒鼠强中毒临床疗效优于单纯二巯基丙醇和常规救治措施，可以明显降低患者B—EP、ET、NO与TNF水平，可作为治疗急性鼠毒强中毒的一种较为理想方案。
- 更多网络解释与毒基相关的网络解释 [注：此内容来源于网络，仅供参考]
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abrin：相思豆毒蛋白
与蓖麻毒蛋白相似结构的所有相思豆毒蛋白(Abrin),此类毒蛋白与细胞表面的乳糖残基单糖受结合是共同的,结合部位包括二个以上的糖. 用神经氨酸处理细胞,可增加结合部位,已经证明:肿瘤细胞表面的单糖链与正常细胞有区别,
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Curare, alkaloids of; curare bases：箭毒生物硷;箭毒基质
cupellation method 烤钵试金法 | Curare, alkaloids of; curare bases 箭毒生物硷;箭毒基质 PP-S1,S3 | Curculigoside 仙茅□
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Michelangelo：米开朗基罗
"米开朗基罗"(Michelangelo)病毒出现后感染所有类型的磁碟. 但是,该病毒的散播范围比媒体预先估计的要小一些. Satanbug病毒具有很强的反杀毒软件功能:该变种能够检查到四种杀毒软件,并且破坏相关磁碟. 这是杀毒软件研究人员历史上第一次和美国联邦调查局(FBI)联手逮捕并且起诉了这个还是孩子的病毒编写者
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digoxige, nin：洋地黄毒苷,地高辛配基
diglyceride甘油二酯 | digoxige,nin洋地黄毒苷,地高辛配基 | digoxin异羟基洋地黄毒苷原,地高辛
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auxotox：助毒基;助毒团
auxoplosophore 助爆基;助爆团 | auxotox 助毒基;助毒团 | available chlorine 有效氯<量>
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auxotox：成毒基
auxotox radical | 甲亚氨基 | auxotox | 成毒基 | auxotroph | 营养缺陷型, 营养缺陷体
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Bufo：蟾蜍屬
"上述特征与蟾蜍属(Bufo)动物完全一致. 化学成分 1.强心甾体化合物为结构类似强心甙而有毒性的蟾毒配基类化合物,已知有10余种,大多是干燥加工过程中的分解产物,如华蟾毒配基约5%,脂蟾毒配基约3.4%,蟾毒灵约1.8%,羟基华蟾毒基约1.6%,
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bufotalin：蟾毒配基
已知有10余种,大多为干燥加工过程中的分解产物,如华蟾毒配基约5%,脂蟾毒配基约3.4%,蟾毒灵约1.8%,羟基华蟾毒基约1.6%,蟾毒配基(bufotalin)约1.5%,远华蟾毒基(telocinobufagin)约1.4%及海蟾蜍精(marinobufagin)等;
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Gitoxigenin：吉妥辛配基 羟基洋地黄毒甙元配基
gitostin 吉托司廷 | gitoxigenin 吉妥辛配基 羟基洋地黄毒甙元配基 | gitoxin 羟基洋地黄毒甙 吉妥辛
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gitoxin：羟基洋地黄毒甙 吉妥辛
gitoxigenin 吉妥辛配基 羟基洋地黄毒甙元配基 | gitoxin 羟基洋地黄毒甙 吉妥辛 | gitoxincellobioside 纤维二糖羟基洋地黄毒甙