查询词典 B. G.
- 与 B. G. 相关的网络例句 [注:此内容来源于网络,仅供参考]
-
Q: The balls of A and B lie near each other through the green. A plays and in doing so affects Bs area of intended stance (e.g., by creating a divot hole).
问:A和B的球都停在果岭通道,彼此离的很近。A打球会影响B站立姿势的区域(比如通过制造一块削起的草皮)。
-
The results indicated that 0.3% brackish water could be used for growing melon without any yield losses,but fruit yield reductions were significant(P.01) during straw period and flor-fruit period and(P.01) during fruitage at 5,7 and 9 g/L.The salinity improved quality during fruitage and decreased quality b...
结果表明,在不同生育时期3 g/L咸水处理对甜瓜产量均无显著影响,在开花坐果期和伸蔓期至果实成熟期,5,7,9 g/L咸水处理的单果重均极显著低于对照,而在果实发育期各咸水处理的单果重均显著低于对照;在甜瓜果实发育期以前,不同浓度咸水处理使甜瓜品质稍有降低,而后期处理则能提高甜瓜果实的品质,其中可溶性蛋白含量的变化不大;伸蔓期至果实成熟期持续咸水处理对甜瓜营养生长有明显的抑制作用,其中对株高的影响表现得尤为突出。
-
2 Presser Foot, Types A, B, C, D, DO, E, O, OO, OOO, and OOO-S, with an orifice (to allow for the protrusion of the indentor) having a diameter as specified in Fig.
A型,B型,C型,D型,DO型,E型,O型,OO型,OOO型,OOO-S型的压足和配合孔的尺寸见FIG.1(a,b,c,d,e,f和g)的规定,压足中心与测量试样任意边缘最小距离为6.0mm(0.24in),当压足设计成圆形平面时,它的的面积不应小于500mm2 19.7in2
-
The standards specify several types of end user access circuits, each of which involves one or more B channels and one D channel. The B channels are for circuit-switched user communications, and the D channels are primarily for signaling and control (e.g., on-hook and off-hook signaling, ringing signals, performance monitoring, synchronization and error control).
该标准详细列出了几种终端用户电路类型,每一种类型包含一个或多个B信道以及1个D信道。B信道用于电路交换用户通信,D信道主要用于信令和控制(例如挂和摘机机信令、振铃信号、性能监控、同步以及错误控制)。
-
A method to construct an interpolation curve of rational quadratic B-spline G continuity is given.
给出二次有理B样条G2连续拼接的条件,提出一种二次有理B样条G2连续插值曲线的构造方法。
-
After that, all samples were fixed with 10 g/L paraform for 45 minutes. Then 50 μL well-fixed blood was added into the polystyrene tube, meanwhile 20 μL monoclonal antibody, such as CD42a-b-c-d and PE-labeled CD42b, was respectively mixed gently with the blood sample and incubated at room temperature in dark for 30 minutes.
取50 μL固定后全血加至流式检测管,同时分别向不同管中加入20 μL糖蛋白Ib/IX/V 复合物单克隆抗体CD42a-b-c-d和PE标记的糖蛋白Ibα单克隆抗体CD42b,混匀后室温避光孵育30 min,然后CD42a-b-c-d标记的样品中加入20 μL FITC标记的羊抗鼠 IgG,混匀后室温避光孵育30 min。
-
Methods: Diabetic nephropathy rats induced by intraperitoneal injection of STZ were randomized into PN model group, n=10, Vitamin B6 group (group B, n=10) and aminoguanidine group (group A, n=10), contrasted to anormal control group (group C, n=10). Aminoguqnidine and VitB6 with 1 g dissolved in 1 L distilled water were given to group A and B, while group C and D only had 1 L disstided water. All groups drunk water freely after 24 hours.
利用链脲菌素腹腔注射法诱导建立DN大鼠模型,将其随机分为模型组、维生素B6治疗组、氨基胍治疗组,并与正常对照组比较,每组10只大鼠;A、B组每天分别用氨基胍、维生素B61g溶于1L蒸馏水中,C、D组仅给予1L蒸馏水,24h后自由饮用。
-
In this thesis, a S~(2-) modified B-Z oscillating system has been successfully used to determine some heavy metal ions and through examining the influence of S~(2-) and benzylpenicillin sodium on B-Z chemical oscillating reaction highly sensitive detection methods of them have been developed.
本文主要研究了利用硫离子修饰的B-Z化学振荡体系对一些重金属离子的测定;同时利用经典的B-Z化学振荡体系对非金属硫离子进行了测定,并考察了药物青霉素G钠盐对该体系的动力学扰动行为。
-
The poly- 2-(dimethylamino ethyl methacrylate-b- potassium polyacrylate (PDMAEMA-b-PPA) with pH and temperature response was polymerized by Reversible Addition-fragmentation Transfer.
具体的过程与结果如下:通过可逆加成-裂解链转移法(Reversible Addition-fragmentation Transfer,RAFT)制备嵌段聚合物PDMAEMA-b-PPA,分子量为24500 g/mol,分布为1.10。
-
The summary results are below:1. GUS expression under the driving of the BjCHI1 promoter (-1060/+17) was essentially undetectable in the young seedlings under normal growth conditions. GUS activity was first detected in the stigma of young flowers, peaked in the young siliques, and decreased when the siliques became older. No GUS expression was found in the mature siliques, seeds or root.2. The BjCHI1 promoter (-1060/+17) was inducible by NaCl, PEG, wounding and MeJA treatments. High levels of GUS expression were detected in the transgenic tobacco and Arabidopsis plants after wounding, NaCl, PEG, and MeJA treatment, indicating that the BjCHI1 promoter responses to both biotic and abiotic stresses.3. RT-PCR analysis confirmed that the expression of the BjCHI1 gene in B. juncea was inducible by PEG and NaCl.4. The transcription start site was determined by 5′-RACE, and was located at the 17th nucleotide upstream of the translation initiation codon of the BjCHI1 gene.5. A -805/+17 promoter fragment was enough to response to wounding and MeJA induction, which was proved in transgenic tobacco and Arabidopsis plants. The 397 bp region between -805 and -409 of the BjCHI1 promoter contains a cis-acting element that is essential for the wounding and MeJA inducibility.6. The -695/-620 region was necessary but not sufficient to confer MeJA-responsive expression. A T/G-box locates in -353 play an important role in the expression of the BjCHI1 gene in response to MeJA treatment. The 76 bp region is coupled with the T/G-box to confer full MeJA-inducible transcription of the BjCHI1 gene.
主要结果如下:1、利用转基因拟南芥植株分析表明,正常生长条件下,BjCHI1启动子(-1060/+17)驱动GUS基因主要在花柱中表达,幼嫩的荚也有表达,并随着果荚的成熟而减弱,成熟的果荚、种子和根没有显示GUS活性。2、BjCHI1启动子(-1060/+17)能驱动GUS基因在转基因烟草和拟南芥中响应伤害的诱导,转基因拟南芥的分析还证明BjCHI1启动子也受MeJA、NaCl和PEG的诱导,证明BjCHI1启动子是一个伤害、MeJA、NaCl和PEG等生物和非生物因素诱导启动子。3、RT-PCR进一步证明芥菜中BjCHI1基因也受NaCl和PEG的诱导表达。4、5′-RACE法鉴定了BjCHI1启动子的转录起始位点,位于翻译起始位点ATG上游第17个碱基A.5、转基因烟草和拟南芥分析证明,-805/+17的启动子片段足以响应伤害和MeJA的诱导,-805和-409之间397 bp的启动子片段含有对伤害和MeJA诱导必要的元件。6、本明烟叶片瞬时表达系统分析证明,一段76 bp的序列(-695/-620)对BjCHI1启动子响应MeJA的诱导是必要的,但不足以响应MeJA的诱导,位于-353的T/G-box也参与MeJA的诱导。76 bp的序列(-695/-620)与T/G-box协同起作用,赋予BjCHI1启动子MeJA诱导性。
- 相关中文对照歌词
- J.B.G.
- Silent B.G.
- With Tha B.G.
- B.H.G.P.S.A.
- B.F.G.F.
- G.B.O.H.
- K.I.S.S.I.N.G. Part B
- B.I.G.T.I.M.E.
- Girls L.G.B.N.A.F.
- Letter To B.I.G.
- 推荐网络例句
-
This one mode pays close attention to network credence foundation of the businessman very much.
这一模式非常关注商人的网络信用基础。
-
Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.
扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。
-
There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.
双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。