ssDNA

The accumulation mechanism of ssDNA on the modified GCE is discussed .

讨论了单链DNA在电化学修饰玻碳电极上的富集机理。

Flow cytometry was used to monitor the affinity of the ssDNA binding to the target cell .

应用流式细胞术监测进化中的文库与A549细胞的结合情况。

Fabrication and Voltammetric Characteristics of Carbon Paste Electrode Modified by ssDNA / Stearic Acid

ssDNA/十八酸修饰碳糊电极的制备及伏安法表征

With the increasing ssDNA concentration , the oxidation peak current of VB2 decreases .

随ssDNA浓度的增加，VB2的氧化峰电流下降。

High Efficient Yeast Transformation by LiAc / ssDNA / PEG

LiAc/ssDNA/PEG法高效转化酵母

Study on Immobilization of ssDNA onto Au Electrode Coating Aminoethanethiol Monolayer

单链DNA在氨基乙硫醇单分子膜金电极上固定化的研究

Immobilization of ssDNA and Its Interaction with Protein

ssDNA的固定化及其与蛋白质相互作用的研究

The Growth and Micro-actuating Behavior of Polypyrrole Films Doped with ssDNA

ssDNA掺杂下聚吡咯薄膜增长及其电化学微致动行为

Furthermore , paralleled ssDNA arrays and their crossover structures have been obtained under our preparation condition .

而且，在一定浓度下获得了平行DNA单链和它们的交叉结构。

SsDNA purification enhanced the fragments recovering from sliver stained denature PAGE gel

单链DNA纯化对变性PAGE凝胶银染片段回收效率的提高

A Procedure for SELEX Screening Aptamers From ssDNA Random Library

随机单链DNA文库SELEX筛选寡核苷酸适配子方法的建立

Interaction Between Gold Nanoparticles and ssDNA

金纳米粒子与单链DNA的相互作用

Study on DNA biosensor based on immobilization ssDNA by avidin-biotin system with differential pulse voltammetry and square wave voltammetry

差分脉冲和方波伏安法研究亲和素-生物素固载ssDNA的生物传感器

Experimental conditions , such as NaCl concentrations , ssDNA concentrations , aggregation time after the addition of salt were optimized .

本研究优化了实验条件，包括盐浓度，单链DNA浓度和加盐之后聚集时间。

With the ssDNA as probe on the electrode surface , we can detect the frequency change and show it on the computer display .

将单链DNA作为探针点在电极表面，测量晶振频率的改变量，并设计出后续处理电路。

Anti ssDNA antibody may be induced by nuclear antigen released from apoptotic cells mediated by Fas / FasL .

由Fas/FasL启动淋巴细胞凋亡产生的核抗原，可致机体产生抗单链DNA抗体。

The serum antibodies recognizing ssDNA and dsDNA of the group increased significantly ( P < ( 0.05 ) . )

血清抗ssDNA抗体、抗dsDNA抗体较对照组和其它实验组显著升高（P<0.05）。

The binding affinity between ssDNA library of each round and SGC-7901 gastric cancer cells was determined by digoxigenin-anti-digoxigenin-AP system .

利用地高辛-抗地高辛抗体-碱性磷酸酶系统测定每轮ssDNA文库与胃癌细胞的亲和力。

RESULTS : The apoptotic cells could be differentiated from non apoptotic cells by the HIC staining with anti ssDNA mAb .

结果：以抗ssDNAmAb建立的检测细胞凋亡的免疫组化法，能够区分凋亡细胞和非凋亡细胞。

This efficient method is suitable for DNA sequence analysis , for the preparation of ssDNA probes , and potentially useful in studies of genomic structural organization .

此法不仅适用于疾病研究中的DNA测序，还可制各单链DNA探针，更利于基因结构组成的研究。

In this way , each ssDNA can go through many cycles , resulting in cleavage of many beacons , achieving a signal amplification .

以这种方式，每条单链DNA可以多次循环使多个分子信标被切开，从而实现信号放大。

Single stranded DNA ( ssDNA ) of 100 bases was adsorbed onto flat gold surface fabricated by depositing gold onto mica surface .

首先通过将金沉积到云母表面制备了表面粗糙度小于0.3nm的金膜，然后一段硫代的单链DNA（100bases）吸附到金膜表面。

Cyclic voltammetry was used to characterize the ssDNA immobilization and hybridization with its complementary DNA sequences by using methylene blue as indicator .

在硬脂酸铝离子膜上进行DNA探针的固定和与目标基因的杂交。

The nanoprobes are composed of single-stranded DNA ( ssDNA ) and Au NPs .

纳米探针是由单链DNA和AuNPs组成。

According to Wu ′ s experimental data of ssDNA chip , the ssDNA biofilm height and the flexoelectric coefficient are fitted .

根据Wu的ssDNA芯片实验数据，对生物膜高度和弯电系数等模型参数进行了拟合，考察了ssDNA链片段长度和封装密度等因素对芯片挠度的影响。

Means To detect the electronic signal with different indictors respectively on ssDNA , completely complementary dsDNA and incompletely complementary hybridization dsDNA .

方法使用不同指示剂，分别检测单链DNA电极在完全互补与三碱基错配DNA中的电化学信号。

The details are summarized as follows : 1 . Investigation of affinities between single strand DNA ( ssDNA ) and SWNTs in water .

具体内容如下：1.单链DNA与碳纳米管在水溶液中的相互作用研究。

The rate constants of chloroquine phosphate with dsDNA and ssDNA were estimated by fitting the real-time experimental data of capacitive sensor . 3 .

通过拟合电容传感器实时响应实验数据，得到了磷酸氯喹与dsDNA和ssDNA的反应速率常数。

It is revealed that ssDNA can sequentially form network , straight chains and layer structures when the adsorption temperature was increased from room temperature to55 ℃ .

结果表明当温度从室温升高到55℃时，单链DNA能依次地形成网状结构、直线状结构和层结构。

Further AFM observation of the layer structures revealed that they are composed of parallel ssDNA chains with relatively higher height and tend to form patterns with three fold symmetry .

进一步研究表明DNA层结构是由高度相对较高的平行单链DNA盘绕而成，并倾向于形成三重对称模式。